Gene: Gpr132 ENSRNOG00000013914

Description

G protein-coupled receptor 132 [Source:RGD Symbol;Acc:1310817]

Gene Synonyms

G2a, LOC314480

Location

Primary_assembly 6: 137,745,241-137,763,157 reverse strand.

GRCr8:CM070396.1

About this gene

This gene has 3 transcripts (splice variants), 32 orthologues, 5 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000110419.2	Gpr132-203	2589	402aa	ENSRNOP00000095175.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AM45	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000018613.5	Gpr132-201	2402	376aa	ENSRNOP00000018613.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KBW8 D3ZIH1	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000094889.2	Gpr132-202	2176	384aa	ENSRNOP00000087645.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A964	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,