PROKR2

prokineticin receptor 2
OMIM: 607123, ClinGen, DECIPHER

8 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 8 panels
Green PROKR2 in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 1.6	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hypogonadotropic hypogonadism 3 with or without anosmia, MIM# 244200
Green PROKR2 in Mendeliome Version 1.2302	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hypogonadotropic hypogonadism 3 with or without anosmia, MIM# 244200
Amber PROKR2 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.540	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Hypogonadotropic hypogonadism 3 with or without anosmia, MIM# 244200
Green PROKR2 in Primary Ovarian Insufficiency_Premature Ovarian Failure Level 3: Gonadal and sex development disorders Level 2: Endocrine disorders Version 0.339	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Victorian Clinical Genetics Services Phenotypes Hypogonadotropic hypogonadism 3 with or without anosmia, MIM# 244200
Green PROKR2 in Pituitary hormone deficiency Level 2: Endocrine disorders Version 0.35	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Genomics England PanelApp Phenotypes Hypogonadotropic hypogonadism 3 with or without anosmia (244200)
Green PROKR2 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Hypogonadotropic hypogonadism
Red PROKR2 in Growth failure Version 1.76	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Genomics England PanelApp Phenotypes Hypogonadotropic hypogonadism 3 with or without anosmia MIM# 244200 Kallmann syndrome (KS) normosmic idiopathic hypogonadotropic hypogonadism (nIHH) Anosmia GnRH deficiency cleft lip and palate renal agenesis Hypogonadotropic hypogonadism low testosterone/ estradiol Absent/ partial Puberty Hearing loss
Red PROKR2 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene Phenotypes Hypogonadotropic hypogonadism 3 with or without anosmia, MIM# 244200