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Gene: Grik4 (glutamate receptor, ionotropic, kainate 4) Mus musculus
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Symbol: Grik4
Name: glutamate receptor, ionotropic, kainate 4
Description: Predicted to have kainate selective glutamate receptor activity and transmitter-gated ion channel activity involved in regulation of postsynaptic membrane potential. Predicted to be involved in glutamatergic synaptic transmission and modulation of chemical synaptic transmission. Localizes to the hippocampal mossy fiber to CA3 synapse and integral component of plasma membrane. Is expressed in brain; hippocampus; hippocampus CA3; telencephalon; and thalamus. Orthologous to human GRIK4 (glutamate ionotropic receptor kainate type subunit 4); PARTICIPATES IN glutamate signaling pathway; INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 3,4-methylenedioxymethamphetamine; 4,4'-sulfonyldiphenol.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: 6330551K01Rik; GluK4; GluRgamma1; glutamate receptor ionotropic, kainate 4; glutamate receptor KA1; glutamate receptor, ionotropic kainate 4; KA-1; KA1
Orthologs:
Latest Assembly: GRCm38 - Mouse Genome Assembly GRCm38
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm38942,518,182 - 42,945,000 (-)NCBIGRCm38GRCm38mm10GRCm38
MGSCv37942,328,519 - 42,752,454 (-)NCBIGRCm37mm9NCBIm37
MGSCv36942,271,429 - 42,695,366 (-)NCBImm8
Celera939,769,298 - 40,069,762 (-)NCBICelera
Cytogenetic Map9 A5.1NCBI
cM Map923.8NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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References - curated
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Genomics

Comparative Map Data
Position Markers
QTLs in Region (GRCm38)
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
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Additional Information

External Database Links
 
More on Grik4
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: mm9 mm10
MGI Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 10683
Created: 2000-05-25
Species: Mus musculus
Last Modified: 2019-11-27
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.