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: Grin2c ENSRNOG00000003280

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Description

glutamate ionotropic receptor NMDA type subunit 2C [Source:RGD Symbol;Acc:2739]

Gene Synonyms

GluN2C, NR2C

Location

Primary_assembly 10: 100,987,513-101,005,409 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 322 orthologues and 17 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000004477.7	Grin2c-201	4567	1250aa	ENSRNOP00000004477.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JSH8 A6HKL2	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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