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: zgc:110591 ENSDARG00000056233

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Description

zgc:110591 [Source:NCBI gene;Acc:402849]

Gene Synonyms

im:6903984

Location

Chromosome 7: 19,909,774-19,923,249 reverse strand.

GRCz11:CM002891.2

About this gene

This gene has 3 transcripts (splice variants), 178 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000078694.4	zgc:110591-201	1918	219aa	ENSDARP00000073155.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7T392	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,
ENSDART00000144180.2	zgc:110591-203	927	106aa	ENSDARP00000114507.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QH73	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000140102.2	zgc:110591-202	727	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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