USH1G gene homepage

General information
Gene symbol USH1G
Gene name Usher syndrome 1G (autosomal recessive)
Chromosome 17
Chromosomal band q25.1
Imprinted Unknown
Genomic reference NC_000017.10
Transcript reference NM_173477.2
Associated with diseases 500004
Citation reference(s) -
Curators (1) Lishuang Shen
Total number of public variants reported 37
Unique public DNA variants reported 37
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
Date created December 10, 2013
Date last updated December 10, 2013
Version USH1G:131210

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 16356
Entrez Gene 124590
PubMed articles USH1G
OMIM - Gene 607696
OMIM - Diseases 500004 (RETINITIS PIGMENTOSA-DEAFNESS SYNDROME )
HGMD USH1G
GeneCards USH1G
GeneTests USH1G


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00003185 17 Usher syndrome 1G (autosomal recessive) NM_173477.2 NP_775748.2 37


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