Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Gna12 ENSRNOG00000001235

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Description

G protein subunit alpha 12 [Source:RGD Symbol;Acc:71018]

Gene Synonyms

Hg1m1

Location

Primary_assembly 12: 18,919,629-19,000,185 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 1 transcript (splice variant), 236 orthologues, 14 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000001654.9	Gna12-201	3345	379aa	ENSRNOP00000001654.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q45QM2 Q45QM3 Q63210	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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Paralogues

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