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: rassf4a ENSDARG00000012460

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Description

Ras association domain family member 4a [Source:ZFIN;Acc:ZDB-GENE-050102-3]

Gene Synonyms

rassf4, zgc:92261

Location

Chromosome 13: 30,664,819-30,700,460 reverse strand.

GRCz11:CM002897.2

About this gene

This gene has 3 transcripts (splice variants), 170 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000139073.3	rassf4a-203	1378	317aa	ENSDARP00000113433.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B8JII7	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,
ENSDART00000126835.4	rassf4a-201	2550	211aa	ENSDARP00000109754.2	Nonsense mediated decay	Q5M7X7	-
ENSDART00000134354.2	rassf4a-202	463	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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