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
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: Gpr137c ENSRNOG00000026328

.

Description

G protein-coupled receptor 137C [Source:RGD Symbol;Acc:1563070]

Gene Synonyms

LOC305812, RGD1563070

Location

Primary_assembly 15: 20,905,958-20,970,541 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000036235.8	Gpr137c-201	2271	423aa	ENSRNOP00000031370.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZFP1	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,
ENSRNOT00000130843.1	Gpr137c-202	2145	381aa	ENSRNOP00000106839.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Summary

.

.