Cataract (Version 0.373)

List	Entity	Reviews	Mode of inheritance	Details
Filter Entities 201 Entitiess
Green List (high evidence)	ABHD12	2 reviews 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract, MIM# 612674 Tags
Green List (high evidence)	ADAMTS10	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	ADAMTS17	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Expert Review Green Phenotypes Weill-Marchesani 4 syndrome, recessive, MIM# 613195 Tags
Green List (high evidence)	AGK	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Sengers syndrome, MIM#212350 Cataract 38 MIM#614691 Tags
Green List (high evidence)	AGPS	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	ALDH18A1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	ANAPC1	3 reviews 3 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Rothmund Thomson syndrome type 1, OMIM 618625 Tags deep intronic
Green List (high evidence)	B3GLCT	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	BCOR	1 review 1 green	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Microphthalmia, syndromic 2, MIM# 300166 Oculofaciocardiodental syndrome Lenz microphthalmia Tags
Green List (high evidence)	BFSP1	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 33, multiple types, MIM# 611391 Tags
Green List (high evidence)	BFSP2	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 12, multiple types, MIM# 611597 Tags
Green List (high evidence)	CHMP4B	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 31, multiple types MIM#605387 Tags
Green List (high evidence)	COG4	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Saul-Wilson syndrome, OMIM #618150 Congenital disorder of glycosylation, type IIj, OMIM #613489 Tags
Green List (high evidence)	COL11A1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	COL18A1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	COL2A1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	COL4A1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	CRYAA	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 9, multiple types, MIM# 604219 Tags
Green List (high evidence)	CRYAB	1 review 1 green	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	CRYBA1	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 10, multiple types, MIM# 600881 Tags
Green List (high evidence)	CRYBA4	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 23, MIM# 610425 Tags
Green List (high evidence)	CRYBB1	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 17, multiple types, MIM# 611544 Tags
Green List (high evidence)	CRYBB2	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 3, multiple types, MIM# 601547 Tags
Green List (high evidence)	CRYBB3	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 22, MIM# 609741 Tags
Green List (high evidence)	CRYGC	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 2, multiple types, MIM# 604307 Tags
Green List (high evidence)	CRYGD	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 4, multiple types, MIM# 115700 Tags
Green List (high evidence)	CRYGS	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 20, multiple types MIM#116100 Tags
Green List (high evidence)	CTDP1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Congenital cataracts, facial dysmorphism, and neuropathy, MIM# 604168 Tags deep intronic founder
Green List (high evidence)	CYP27A1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	CYP51A1	1 review 1 green	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Congenital cataract infantile liver disease Tags
Green List (high evidence)	DHCR7	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	DNMBP	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes congenital cataract Tags
Green List (high evidence)	DPAGT1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Expert Review Green Phenotypes Congenital disorder of glycosylation, type Ij, MIM# 608093 DPAGT1-CDG MONDO:0011964 Tags
Green List (high evidence)	EIF2B2	2 reviews 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes leukodystrophy congenital cataracts Leukoencephalopathy with vanishing white matter, MIM# 603896 Tags
Green List (high evidence)	EPG5	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Expert Review Green Phenotypes Vici syndrome, MIM# 242840 Tags
Green List (high evidence)	EPHA2	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 6, multiple types, MIM# 116600 Tags
Green List (high evidence)	ERCC2	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	ERCC3	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	ERCC6	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	ERCC8	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	FAM126A	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	FAR1	2 reviews 2 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Cataracts, spastic paraparesis, and speech delay, MIM#619338 Peroxisomal fatty acyl-CoA reductase 1 disorder, MIM# 616154 Tags
Green List (high evidence)	FBN1	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Marfan syndrome, MIM# 154700 Weill-Marchesani syndrome 2, dominant, MIM# 608328 Tags
Green List (high evidence)	FOSL2	2 reviews 2 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Aplasia cutis-enamel dysplasia syndrome, MIM# 620789 Tags
Green List (high evidence)	FOXE3	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	FTL	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	FYCO1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 18, MIM#610019 Tags
Green List (high evidence)	GALK1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags treatable
Green List (high evidence)	GALM	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes galactosaemia type IV galactosaemia Tags
Green List (high evidence)	GALT	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags treatable
Green List (high evidence)	GCNT2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 13 with adult i phenotype, OMIM # 116700 Tags
Green List (high evidence)	GEMIN4	2 reviews 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities, 617913 Tags
Green List (high evidence)	GFER	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay MIM#613076 Tags
Green List (high evidence)	GJA3	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	GJA8	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 1, multiple types, MIM# 116200 Microphthalmia Tags
Green List (high evidence)	GNPAT	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	GTF2H5	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Trichothiodystrophy 3, photosensitive (MIM# 616395) Tags
Green List (high evidence)	HMX1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	HSF4	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 5, multiple types, 116800 Tags
Green List (high evidence)	HTRA2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes 3-methylglutaconic aciduria type VIII (617248) Tags
Green List (high evidence)	INPP5K	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	INTS1	2 reviews 2 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies, MIM# 618571 Tags
Green List (high evidence)	ISPD	2 reviews 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7 MIM#614643 Tags
Green List (high evidence)	JAM3	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730 Tags
Green List (high evidence)	LIM2	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 19, multiple types, MIM# 615277 Tags
Green List (high evidence)	LONP1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes CODAS syndrome MIM# 600373 Tags
Green List (high evidence)	LSS	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Cataract 44 MIM#616509 Tags
Green List (high evidence)	MAF	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	MAN2B1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	MED27	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia, MIM# 619286 Tags
Green List (high evidence)	MIP	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	MIR184	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes EDICT syndrome, MIM# 614303 Tags
Green List (high evidence)	MSMO1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Green Phenotypes Microcephaly, congenital cataract, and psoriasiform dermatitis MIM#616834 MONDO:0014793 Tags
Green List (high evidence)	MYH9	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	NACC1	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination delayed brain myelination (MIM# 617393) Tags
Green List (high evidence)	NDP	1 review 1 green	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Norrie disease (MIM# 310600) Tags
Green List (high evidence)	NF2	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Neurofibromatosis, type 2 (MIM# 101000) Tags
Green List (high evidence)	NHS	1 review 1 green	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Nance-Horan syndrome (MIM# 302350) Tags
Green List (high evidence)	NUP188	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Sandestig-Stefanova syndrome, 618804 microcephaly ID cataract structural brain abnormalities hypoventilation Tags
Green List (high evidence)	OAT	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Green Phenotypes Gyrate atrophy of choroid and retina with or without ornithinemia MIM#258870 Tags
Green List (high evidence)	OCRL	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	OPA3	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	P3H2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Myopia, high, with cataract and vitreoretinal degeneration - MIM#614292 Tags
Green List (high evidence)	PAX6	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX10	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX11B	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX12	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX13	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX14	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX16	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX19	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX2	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX26	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX3	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX5	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX6	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX7	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PIK3C2A	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Oculoskeletodental syndrome, MIM# 618440 Tags
Green List (high evidence)	PISD	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PITX3	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PLOD3	2 reviews 2 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes cataract Tags
Green List (high evidence)	POLG	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes POLG-related disorders Tags
Green List (high evidence)	POMT2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PXDN	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400 Tags
Green List (high evidence)	RAB18	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Warburg micro syndrome 3, MIM# 614222 Tags founder
Green List (high evidence)	RAB3GAP1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Warburg micro syndrome 1, MIM# 600118 Martsolf syndrome 2, MIM# 619420 Tags
Green List (high evidence)	RAB3GAP2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Warburg micro syndrome 2, MIM# 614225 Tags
Green List (high evidence)	SC5D	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Lathosterolosis, MIM# 607330 Tags
Green List (high evidence)	SIL1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Marinesco-Sjogren syndrome (MIM#248800) Tags
Green List (high evidence)	SLC16A12	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 47, juvenile, with microcornea 612018 Tags
Green List (high evidence)	SLC2A1	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	SLC33A1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Congenital cataracts, hearing loss, and neurodegeneration, MIM# 614482 Tags
Green List (high evidence)	SRD5A3	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	SREBF1	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Expert Review Green Phenotypes Mucoepithelial dysplasia, hereditary, MIM#158310 Tags
Green List (high evidence)	TDRD7	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cataract 36 613887 glaucoma nonobstructive azoospermia arrested spermatogenesis Tags
Green List (high evidence)	TFAP2A	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	VIM	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	VSX2	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	WFS1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Green Phenotypes Wolfram syndrome 1, MIM# 222300 Tags
Green List (high evidence)	WRN	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	XYLT2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Green Phenotypes Spondyloocular syndrome, MIM# 605822 Tags
Green List (high evidence)	ZNF526	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Dentici-Novelli neurodevelopmental syndrome, MIM# 619877 Tags
Amber List (moderate evidence)	ADD3	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Cerebral palsy, spastic quadriplegic, 3 617008 Tags
Amber List (moderate evidence)	COL4A2	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Cataract (MONDO:0005129), COL4A2-related Tags
Amber List (moderate evidence)	COL9A1	2 reviews 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Stickler syndrome, type IV, MIM#614134 Tags
Amber List (moderate evidence)	COPB1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Baralle-Macken syndrome, MIM# 619255 Severe intellectual disability variable microcephaly cataracts Tags
Amber List (moderate evidence)	DNA2	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Rothmund-Thomson syndrome, type 4, MIM# 620819 Tags
Amber List (moderate evidence)	ESCO2	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Craniofacial abnormalities Developmental Delay Corneal opacities Growth retardation Limb abnormalities Roberts syndrome 238300 Tags
Amber List (moderate evidence)	FKRP	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 5 Muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation) type B, 5 Muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 5 Tags
Amber List (moderate evidence)	FKTN	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Limb Girdle Muscular Dystrophy with No Mental Retardation Congenital Cataract Tags
Amber List (moderate evidence)	GLS	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Amber Phenotypes Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development MONDO:0032685 Tags
Amber List (moderate evidence)	HPS1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Hermansky-Pudlak syndrome 1 (203300) Tags
Amber List (moderate evidence)	HPS4	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Hermansky-Pudlak syndrome 4 (614073) Tags
Amber List (moderate evidence)	HPS6	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Hermansky-Pudlak syndrome 6 (614075) Tags
Amber List (moderate evidence)	IKBKG	1 review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Incontinentia pigmenti (308300) / Ectodermal dysplasia and immunodeficiency 1 (300291) Ectodermal dysplasia, anhidrotic, lymphoedema and immunodeficiency (300301) Immunodeficiency 33 (300636) Immunodeficiency, isolated (300584) Invasive pneumococcal disease, recurrent isolated 2 (300640) Tags
Amber List (moderate evidence)	ITPA	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Epileptic encephalopathy, early infantile, 35, MIM# 616647 Tags
Amber List (moderate evidence)	LARGE1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 6 (MIM# 613154) Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6 (MIM# 608840) Tags
Amber List (moderate evidence)	LCAT	2 reviews 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Tags
Amber List (moderate evidence)	LEMD2	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Cataract 46, juvenile-onset, OMIM# 212500 Tags founder
Amber List (moderate evidence)	LMX1B	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Nail-patella syndrome, MIM# 161200 Tags
Amber List (moderate evidence)	PANK4	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Cataract 49, MIM# 619593 Congenital posterior cataract Tags
Amber List (moderate evidence)	PGRMC1	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Amber Literature Phenotypes Isolated paediatric cataract Tags SV/CNV
Amber List (moderate evidence)	PIK3R1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes SHORT syndrome, MIM# 269880 Tags
Amber List (moderate evidence)	POMT1	1 review	Unknown	Sources Expert Review Amber Victorian Clinical Genetics Services Tags
Amber List (moderate evidence)	PSMC3	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Deafness, cataract, impaired intellectual development, and polyneuropathy, MIM#619354 Tags
Amber List (moderate evidence)	RIC1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Amber Phenotypes CATIFA syndrome, MIM# 618761 Tags
Amber List (moderate evidence)	SIPA1L3	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert list Expert Review Amber Phenotypes Cataract 45 MIM#616851 Tags
Amber List (moderate evidence)	TKFC	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Triokinase and FMN cyclase deficiency syndrome, MIM#618805 Developmental delay cataracts liver dysfunction Tags
Amber List (moderate evidence)	TMEM70	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Amber Phenotypes Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2 MIM#614052 Tags
Amber List (moderate evidence)	TRPM3	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Amber Phenotypes Cataract 50 with or without glaucoma, MIM#620253 Tags
Red List (low evidence)	ADA	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Severe combined immunodeficiency due to ADA deficiency 102700 Tags
Red List (low evidence)	ADAM17	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Inflammatory skin and bowel disease Tags
Red List (low evidence)	ADAMTSL4	2 reviews 2 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes ectopia lentis cataract Tags
Red List (low evidence)	AICDA	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Immunodeficiency with hyper-IgM, type 2 605258 Tags
Red List (low evidence)	AKR1E2	2 reviews 2 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Cataract, MONDO:0005129, AKR1E2-related Tags
Red List (low evidence)	ARL2	1 review 1 red	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Red Phenotypes Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma-1 (MRCS1), MIM#619082 Tags
Red List (low evidence)	BTK	1 review 1 red	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes X-linked agammaglobulinemia isolated growth hormone deficiency type III with agammaglobulinemia Tags
Red List (low evidence)	CD3G	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Immunodeficiency 17, CD3 gamma deficient Tags
Red List (low evidence)	CD40LG	1 review 1 red	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Immunodeficiency with Hyper-IgM type 1 Tags
Red List (low evidence)	COL9A2	2 reviews 1 green 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Stickler syndrome, type V, MIM# 614284 Tags
Red List (low evidence)	CRYGA	1 review 1 red	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Tags disputed
Red List (low evidence)	CYBA	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Chronic granulomatous disease Tags
Red List (low evidence)	CYBB	1 review 1 red	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Chronic granulomatous disease immunodeficiency 34 with mycobacteriosis Tags
Red List (low evidence)	DCLRE1C	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Omenn syndrome 603554 Severe combined immunodeficiency, Athabascan type 602450 Tags
Red List (low evidence)	DOCK8	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Hyper-IgE recurrent infection syndrome 243700 Tags SV/CNV
Red List (low evidence)	DYRK1A	1 review 1 red	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes congenital cataracts Tags
Red List (low evidence)	EED	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Cohen-Gibson syndrome Tags
Red List (low evidence)	EPCAM	1 review 1 red	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Congenital diarrhoea 5 with tufting enteropathy Lynch syndrome Tags
Red List (low evidence)	FOXP3	1 review 1 red	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790 Tags
Red List (low evidence)	GBF1	1 review 1 red	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes autosomal dominant cataract MONDO:0022672, GBF1-related Tags
Red List (low evidence)	GJA1	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Oculodentodigital dysplasia, autosomal recessive, MIM# 257850 Tags
Red List (low evidence)	GUCY2C	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Diarrhea 6, 614616 Meconium ileus, 614665 Tags
Red List (low evidence)	ICOS	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Common variable immunodeficiency 1 (604558) Tags
Red List (low evidence)	IL10	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	IL10RA	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Inflammatory bowel disease 28, early onset (613148) Tags
Red List (low evidence)	IL10RB	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Inflammatory bowel disease 25, early onset (612567) Tags
Red List (low evidence)	IL2RG	1 review 1 red	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Severe combined immunodeficiency, X-linked (300400) Moderate combined immunodeficiency, X-linked (312863) Tags
Red List (low evidence)	ITGB2	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Leukocyte adhesion deficiency (MIM# 116920) Tags
Red List (low evidence)	KAT2B	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes cataract MONDO:0005129, KAT2B-related Tags
Red List (low evidence)	LIG4	2 reviews 2 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	LRBA	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	NCF1	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	NCF2	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	NCF4	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	NSUN2	2 reviews 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Mental retardation, autosomal recessive 5, MIM# 611091 Severe intellectual disability, microcephaly, postnatal growth retardation, and dysmorphic facial features Tags
Red List (low evidence)	PLCG2	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	RAG2	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	RET	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	RGS6	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Neurodevelopmental disorder, MONDO:0700092, RGS6-related Tags
Red List (low evidence)	RNH1	3 reviews 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Neurodevelopmental disorder, MONDO:0700092, RNH1-related Tags
Red List (low evidence)	SH2D1A	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	SKIV2L	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	SLC37A4	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	STXBP2	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	TAPT1	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type (MIM#616897) Tags
Red List (low evidence)	TTC37	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	UBE2U	1 review 1 red	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Retinoschisis cataracts learning disabilities developmental delay Tags
Red List (low evidence)	WAS	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	XIAP	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	ZAP70	1 review 1 red	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags

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