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:ch211-129c21.1 ENSDARG00000024775

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Description

si:ch211-129c21.1 [Source:ZFIN;Acc:ZDB-GENE-030131-5796]

Gene Synonyms

fi18h09, wu:fb73c06, wu:fi18h09

Location

Chromosome 22: 22,316,855-22,340,688 reverse strand.

GRCz11:CM002906.2

About this gene

This gene has 2 transcripts (splice variants), 107 orthologues and 36 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000105597.5	si:ch211-129c21.1-201	2398	775aa	ENSDARP00000096374.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M9MMA2	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,
ENSDART00000144684.2	si:ch211-129c21.1-202	760	115aa	ENSDARP00000115892.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M9MMB2	-

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Summary

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