Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ush1gb ENSDARG00000076079

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Description

Usher syndrome 1Gb (autosomal recessive) [Source:ZFIN;Acc:ZDB-GENE-110411-55]

Gene Synonyms

si:ch73-283g7.2, ush1g

Location

Chromosome 12: 46,582,168-46,598,223 forward strand.

GRCz11:CM002896.2

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000189402.1	ush1gb-202	2038	488aa	ENSDARP00000156275.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8QSI6	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSDART00000149326.2	ush1gb-201	1188	392aa	ENSDARP00000123939.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F8W4A4	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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