Overview

Variant ID 22460
Entrez Gene ID 7399
Gene USH2A (GeneCards)
Location hg19 1:216545986-216545986
hg38 1:216372644-216372644
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000001.10:g.216545986 C>G (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1557
CADD Raw score (version 1.3) -0.130432 (Deleterious)
FATHMM raw prediction score 0.12013 (Tolerated)
Deleterious probability by DeFine 0.2392 (Neutral)
Entrez Gene ID 7399 (NCBI Gene)
Official Gene Symbol USH2A (GeneCards)
Number of variants in USH2A in this database 8 (view all the variants)
Full name usherin
Band 1q41
Other IDs Vega: OTTHUMG00000037079
OMIM: 608400
HGNC: HGNC:12601
Ensembl: ENSG00000042781
Other names US2, RP39, USH2, dJ1111A8.1
Summary This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIa and retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

Individual #1

Individual ID 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
Title Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis.
Journal Science
Publication date 2018.02
Disease Asymptomatic
Number of cases cases of unknown sex: 3;