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: si:ch73-302o18.2 ENSDARG00000088316

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Description

si:ch73-302o18.2 [Source:ZFIN;Acc:ZDB-GENE-120215-213]

Location

Chromosome 19: 33,828,976-33,835,396 reverse strand.

GRCz11:CM002903.2

About this gene

This gene has 3 transcripts (splice variants), 4 orthologues and 32 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000130984.4	si:ch73-302o18.2-201	1091	345aa	ENSDARP00000110106.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FCW6	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,
ENSDART00000151680.2	si:ch73-302o18.2-203	591	160aa	ENSDARP00000126024.1	Nonsense mediated decay	I3ISX4	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000151526.2	si:ch73-302o18.2-202	542	69aa	ENSDARP00000125670.1	Nonsense mediated decay	I3IS07	-

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Summary

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