Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4900
Gene name Gene Name - the full gene name approved by the HGNC.
Neurogranin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NRGN
Synonyms (NCBI Gene) Gene synonyms aliases
RC3, hng
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q24.2
Summary Summary of gene provided in NCBI Entrez Gene.
Neurogranin (NRGN) is the human homolog of the neuron-specific rat RC3/neurogranin gene. This gene encodes a postsynaptic protein kinase substrate that binds calmodulin in the absence of calcium. The NRGN gene contains four exons and three introns. The ex
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT492851 hsa-miR-744-5p PAR-CLIP 23592263
MIRT492850 hsa-miR-665 PAR-CLIP 23592263
MIRT492849 hsa-miR-3940-3p PAR-CLIP 23592263
MIRT492848 hsa-miR-3141 PAR-CLIP 23592263
MIRT492847 hsa-miR-6840-3p PAR-CLIP 23592263
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005516 Function Calmodulin binding IEA
GO:0005516 Function Calmodulin binding TAS 10075657
GO:0005547 Function Phosphatidylinositol-3,4,5-trisphosphate binding IEA
GO:0005829 Component Cytosol TAS
GO:0007165 Process Signal transduction TAS 10075657
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602350 8000 ENSG00000154146
Protein
UniProt ID Q92686
Protein name Neurogranin (Ng) (RC3) [Cleaved into: NEUG(55-78)]
Protein function Acts as a 'third messenger' substrate of protein kinase C-mediated molecular cascades during synaptic development and remodeling. Binds to calmodulin in the absence of calcium (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00612 IQ 27 47 IQ calmodulin-binding motif Motif
Tissue specificity TISSUE SPECIFICITY: In the cerebral cortex, found in the cell bodies of neurons in layers II-VI, and in apical and basal dendrites of pyramidal neurons. Is not found in the dendrites in patients with Alzheimer disease. {ECO:0000269|PubMed:9329454}.
Sequence
MDCCTENACSKPDDDILDIPLDDPGANAAAAKIQASFRGHMARKKIKSGERGRKGPGPGG
PGGAGVARGGAGGGPSGD
Sequence length 78
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Long-term potentiation
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Stimulate 26826204, 27604409, 36142742
Alzheimer Disease Associate 27321472, 29700597, 30342961, 30846386, 32568193, 33765432, 33924468, 35173266, 36142780, 39242539
Alzheimer Disease Inhibit 32776690
Anemia Sickle Cell Associate 33915030
Atrophy Associate 35584575
Brain Diseases Associate 30953482
Brain Injuries Traumatic Stimulate 29717219
Cerebral Infarction Associate 32785988
Cognition Disorders Associate 27321472, 30419087, 32776690
Cognition Disorders Inhibit 39242539