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

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Gene: rassf2a ENSDARG00000029865

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Description

Ras association domain family member 2a [Source:ZFIN;Acc:ZDB-GENE-040912-124]

Gene Synonyms

rassf2, wu:fa04h12, zgc:101844

Location

Chromosome 8: 42,998,944-43,049,069 forward strand.

GRCz11:CM002892.2

About this gene

This gene has 3 transcripts (splice variants), 198 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000048819.8	rassf2a-201	3655	325aa	ENSDARP00000048818.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A9C3N2	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,
ENSDART00000142671.2	rassf2a-202	541	129aa	ENSDARP00000117969.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A9C3N1	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000146632.2	rassf2a-203	902	61aa	ENSDARP00000119164.1	Nonsense mediated decay	E9QBA8	-

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Summary

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