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Prepair 1000+

Gene: LINS1

Green List (high evidence)

LINS1 (lines homolog 1)
EnsemblGeneIds (GRCh38): ENSG00000140471
EnsemblGeneIds (GRCh37): ENSG00000140471
OMIM: 610350, Gene2Phenotype
LINS1 is in 5 panels

2 reviews

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Cassandra Muller (Victorian Clinical Genetics Services)

Well established gene- condition association.
Created: 12 Dec 2024, 1:57 a.m. | Last Modified: 12 Dec 2024, 1:57 a.m.
Panel Version: 1.669

Phenotypes
Intellectual developmental disorder, autosomal recessive 2, 614340 (3)

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Intellectual developmental disorder, autosomal recessive 2, MIM#614340
OMIM
610350
Clinvar variants
Variants in LINS1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

13 Dec 2024, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: lins1 has been classified as Green List (High Evidence).

13 Dec 2024, Gel status: 3

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: LINS1 were changed from Mental retardation, autosomal recessive 27, 614340 (3) to Intellectual developmental disorder, autosomal recessive 2, MIM#614340

13 Dec 2024, Gel status: 3

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: LINS1 were set to

1 Jun 2022, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: LINS1 was added gene: LINS1 was added to Reproductive Carrier Screen_VCGS. Sources: Mackenzie's Mission,Expert Review Green Mode of inheritance for gene: LINS1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: LINS1 were set to Mental retardation, autosomal recessive 27, 614340 (3)