Gene: USH1G ENSG00000182040

Description

Usher syndrome 1G (autosomal recessive) [Source:HGNC Symbol;Acc:16356]

Gene Synonyms

ANKS4A, FLJ33924, SANS, Sans

Location

GRCh37:CM000679.1

About this gene

This gene has 2 transcripts (splice variants), 1 paralogue and is associated with 4 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000319642.1	USH1G-001	3561	461aa	ENSP00000320076.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS32725	Q495M9	NM_173477.2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000579243.1	USH1G-002	1673	115aa	ENSP00000462568.1	Nonsense mediated decay		J3KSN5	-	-

Summary