GRIN2C
glutamate ionotropic receptor NMDA type subunit 2C | GluN2C, NR2C, NMDAR2C

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]

Biological processes 50 terms
NMDA glutamate receptor activity (GO:0004972)NMDA glutamate receptor activity (GO:0004972)NMDA glutamate receptor activity (GO:0004972)NMDA glutamate receptor activity (GO:0004972)NMDA glutamate receptor activity (GO:0004972)NMDA selective glutamate receptor complex (GO:0017146)NMDA selective glutamate receptor complex (GO:0017146)NMDA selective glutamate receptor complex (GO:0017146)NMDA selective glutamate receptor complex (GO:0017146)brain development (GO:0007420)calcium ion transmembrane import into cytosol (GO:0097553)calcium ion transmembrane import into cytosol (GO:0097553)endoplasmic reticulum membrane (GO:0005789)excitatory chemical synaptic transmission (GO:0098976)excitatory postsynaptic potential (GO:0060079)glutamate receptor signaling pathway (GO:0007215)glutamatergic synapse (GO:0098978)ionotropic glutamate receptor signaling pathway (GO:0035235)ligand-gated monoatomic ion channel activity (GO:0015276)long-term synaptic potentiation (GO:0060291)membrane (GO:0016020)modulation of chemical synaptic transmission (GO:0050804)monoatomic cation channel activity (GO:0005261)monoatomic cation transmembrane transport (GO:0098655)monoatomic cation transmembrane transport (GO:0098655)monoatomic ion channel activity (GO:0005216)monoatomic ion transport (GO:0006811)organelle (GO:0043226)plasma membrane (GO:0005886)plasma membrane (GO:0005886)plasma membrane (GO:0005886)plasma membrane (GO:0005886)plasma membrane (GO:0005886)positive regulation of excitatory postsynaptic potential (GO:2000463)positive regulation of synaptic transmission, glutamatergic (GO:0051968)postsynaptic density membrane (GO:0098839)postsynaptic density membrane (GO:0098839)postsynaptic membrane (GO:0045211)postsynaptic membrane (GO:0045211)postsynaptic membrane (GO:0045211)protein binding (GO:0005515)regulation of monoatomic cation transmembrane transport (GO:1904062)regulation of neuronal synaptic plasticity (GO:0048168)regulation of synaptic plasticity (GO:0048167)regulation of synaptic plasticity (GO:0048167)regulation of synaptic plasticity (GO:0048167)signaling receptor activity (GO:0038023)synaptic transmission, glutamatergic (GO:0035249)transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential (GO:1904315)transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential (GO:1904315)
Expression (TPM)
GRIN2C — as a Regulated Gene

TFs regulating GRIN2C 0 TFs

Transcription factors with Perturb-seq knockdown data for GRIN2C. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = GRIN2C upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to GRIN2C

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of GRIN2C, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.

Accessibility Element Dist. to TSS Link type TFs
chr17:74,852,259–74,853,211 8.3 kb Proximal (<10kb) 435
chr17:74,861,383–74,861,945 at TSS At TSS 101
chr17:74,862,113–74,862,501 609 bp At TSS 272
chr17:74,864,803–74,865,168 3.3 kb Proximal (<10kb) 262

Genome Browser

Genomic view of the GRIN2C locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.

chr17:74,842,259 – 74,875,168
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq