GRIN2C

GENERAL INFORMATION

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Gene name

GRIN2C

Gene description

Glutamate receptor, ionotropic, N-methyl D-aspartate 2C

Protein class

FDA approved drug targets
Plasma proteins
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (cerebral cortex, heart muscle, placenta, salivary gland, testis, thyroid gland)
GTEx:Group enriched (cerebellum)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (cerebral cortex, heart muscle, placenta, salivary gland, testis, thyroid gland)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (cerebellum)

Organ

Expression



GENE INFORMATION

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Gene name

GRIN2C (HGNC Symbol)

Synonyms

GluN2C, NMDAR2C

Description

Glutamate receptor, ionotropic, N-methyl D-aspartate 2C (HGNC Symbol)

Entrez gene summary

This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptor, which is a subtype of ionotropic glutamate receptor. NMDA receptors are found in the central nervous system, are permeable to cations and have an important role in physiological processes such as learning, memory, and synaptic development. The receptor is a tetramer of different subunits (typically heterodimer of subunit 1 with one or more of subunits 2A-D), forming a channel that is permeable to calcium, potassium, and sodium, and whose properties are determined by subunit composition. Alterations in the subunit composition of the receptor are associated with pathophysiological conditions such as Parkinson's disease, Alzheimer's disease, depression, and schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]

Chromosome

17

Cytoband

q25.1

Chromosome location (bp)

74842023 - 74861504

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000161509 (version 78.38)

Entrez gene

2905

UniProt

Q14957 (UniProt - Evidence at protein level)

neXtProt

NX_Q14957

Antibodypedia

GRIN2C antibodies


PROTEIN BROWSER

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ENST00000293190
 
ENST00000347612
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

GRIN2C-001 ENSP00000293190
ENST00000293190
Q14957
Show all »
Show » Show » 1233 134.2 Yes 4
GRIN2C-002 ENSP00000338645
ENST00000347612
H0Y2V8
Show all »
Show » Show » 873 96 Yes 4