GRIN2C
Glutamate receptor ionotropic, NMDA 2C
Also known as: GluN2C, NMDAR2C, NMDE3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14957
- Gene
- GRIN2C
- Ensembl
- ENSG00000161509
- Chromosome
- 17
- Canonical length
- 1233 aa
- Protein class
- FDA approved drug targets, Plasma proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
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]
Canonical amino-acid sequenceUniProt
1233 residues, UniProt reviewed canonical sequence.
>Q14957|GRIN2C
1 MGGALGPALL LTSLFGAWAG LGPGQGEQGM TVAVVFSSSG PPQAQFRARL TPQSFLDLPL
61 EIQPLTVGVN TTNPSSLLTQ ICGLLGAAHV HGIVFEDNVD TEAVAQILDF ISSQTHVPIL
121 SISGGSAVVL TPKEPGSAFL QLGVSLEQQL QVLFKVLEEY DWSAFAVITS LHPGHALFLE
181 GVRAVADASH VSWRLLDVVT LELGPGGPRA RTQRLLRQLD APVFVAYCSR EEAEVLFAEA
241 AQAGLVGPGH VWLVPNLALG STDAPPATFP VGLISVVTES WRLSLRQKVR DGVAILALGA
301 HSYWRQHGTL PAPAGDCRVH PGPVSPAREA FYRHLLNVTW EGRDFSFSPG GYLVQPTMVV
361 IALNRHRLWE MVGRWEHGVL YMKYPVWPRY SASLQPVVDS RHLTVATLEE RPFVIVESPD
421 PGTGGCVPNT VPCRRQSNHT FSSGDVAPYT KLCCKGFCID ILKKLARVVK FSYDLYLVTN
481 GKHGKRVRGV WNGMIGEVYY KRADMAIGSL TINEERSEIV DFSVPFVETG ISVMVARSNG
541 TVSPSAFLEP YSPAVWVMMF VMCLTVVAIT VFMFEYFSPV SYNQNLTRGK KSGGPAFTIG
601 KSVWLLWALV FNNSVPIENP RGTTSKIMVL VWAFFAVIFL ASYTANLAAF MIQEQYIDTV
661 SGLSDKKFQR PQDQYPPFRF GTVPNGSTER NIRSNYRDMH THMVKFNQRS VEDALTSLKM
721 GKLDAFIYDA AVLNYMAGKD EGCKLVTIGS GKVFATTGYG IAMQKDSHWK RAIDLALLQF
781 LGDGETQKLE TVWLSGICQN EKNEVMSSKL DIDNMAGVFY MLLVAMGLAL LVFAWEHLVY
841 WKLRHSVPNS SQLDFLLAFS RGIYSCFSGV QSLASPPRQA SPDLTASSAQ ASVLKMLQAA
901 RDMVTTAGVS SSLDRATRTI ENWGGGRRAP PPSPCPTPRS GPSPCLPTPD PPPEPSPTGW
961 GPPDGGRAAL VRRAPQPPGR PPTPGPPLSD VSRVSRRPAW EARWPVRTGH CGRHLSASER
1021 PLSPARCHYS SFPRADRSGR PFLPLFPELE DLPLLGPEQL ARREALLHAA WARGSRPRHA
1081 SLPSSVAEAF ARPSSLPAGC TGPACARPDG HSACRRLAQA QSMCLPIYRE ACQEGEQAGA
1141 PAWQHRQHVC LHAHAHLPFC WGAVCPHLPP CASHGSWLSG AWGPLGHRGR TLGLGTGYRD
1201 SGGLDEISRV ARGTQGFPGP CTWRRISSLE SEVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GRIN2C can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 3
- Mean surface accessibility (rSASA)
- 0.43
- Highest tissue expression
- 114 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 114 nTPM
- basal ganglia: 28 nTPM
- cerebral cortex: 24 nTPM
- amygdala: 24 nTPM
- heart muscle: 18 nTPM
- thyroid gland: 16 nTPM
Single-cell type
- astrocytes: 149 nCPM
- bergmann glia: 58 nCPM
- hofbauer cells: 43 nCPM
- sertoli cells: 33 nCPM
- brain excitatory neurons: 32 nCPM
- retinal amacrine cells: 29 nCPM
Immune cell
- plasmacytoid DC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebellum: 108 nTPM
- pons: 62 nTPM
- basal ganglia: 46 nTPM
- amygdala: 42 nTPM
- cerebral cortex: 41 nTPM
- thalamus: 38 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.72
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.61
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- brain development
- calcium ion transmembrane import into cytosol
- directional locomotion
- excitatory chemical synaptic transmission
- excitatory postsynaptic potential
- glutamate receptor signaling pathway
- ionotropic glutamate receptor signaling pathway
- long-term synaptic potentiation
- monoatomic cation transmembrane transport
- negative regulation of protein catabolic process
- neuromuscular process controlling balance
- positive regulation of excitatory postsynaptic potential
- positive regulation of synaptic transmission, glutamatergic
- protein localization to postsynaptic membrane
- regulation of monoatomic cation transmembrane transport
- regulation of neuronal synaptic plasticity
- regulation of synaptic plasticity
- response to wounding
- synaptic transmission, glutamatergic
Molecular functions
- monoatomic cation channel activity
- NMDA glutamate receptor activity
- transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ionotropic glutamate receptor, C-terminal
- Ionotropic glutamate receptor, metazoa
- Receptor, ligand binding region
- Ionotropic glutamate receptor
- Glutamate [NMDA] receptor, epsilon subunit, C-terminal
- Ionotropic glutamate receptor, L-glutamate and glycine-binding domain
- Periplasmic binding protein-like I
- Ligand-gated ion channel
- Receptor family ligand binding region
- N-methyl D-aspartate receptor 2B3 C-terminus
- Ligated ion channel L-glutamate- and glycine-binding site
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GRIN2C in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GRIN2C as an antibody target. Whether an autoantibody or antibody against GRIN2C could matter depends on whether native GRIN2C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GRIN2C is annotated at the cell surface, where native GRIN2C is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label GRIN2C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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