Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- 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: GARIN1A ENSBTAG00000024291

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Description

golgi associated RAB2 interactor 1A [Source:VGNC Symbol;Acc:VGNC:50126]

Gene Synonyms

FAM71F2

Location

Primary_assembly 4: 92,662,571-92,674,004 forward strand.

ARS-UCD1.3:CM008171.2

About this gene

This gene has 1 transcript (splice variant), 94 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000033556.4	GARIN1A-201	1146	300aa	ENSBTAP00000033468.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N304	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,

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Summary

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