Gene Gene information from NCBI Gene database.
Entrez ID 9454
Gene name Homer scaffold protein 3
Gene symbol HOMER3
Synonyms (NCBI Gene)
HOMER-3VESL3
Chromosome 19
Chromosome location 19p13.11
Summary This gene encodes a member of the HOMER family of postsynaptic density scaffolding proteins that share a similar domain structure consisting of an N-terminal Enabled/vasodilator-stimulated phosphoprotein homology 1 domain which mediates protein-protein in
miRNA miRNA information provided by mirtarbase database.
11
miRTarBase ID miRNA Experiments Reference
MIRT1052599 hsa-miR-1538 CLIP-seq
MIRT1052600 hsa-miR-1915 CLIP-seq
MIRT1052601 hsa-miR-3940-3p CLIP-seq
MIRT1052602 hsa-miR-4685-5p CLIP-seq
MIRT1052603 hsa-miR-4690-3p CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
CEBPA Unknown 14645007
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 16979624, 18218901, 18387811, 19060904, 19345194, 21516116, 21911467, 25416956, 25910212, 26871637, 29892012, 32296183, 33961781, 35271311
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol IEA
GO:0005829 Component Cytosol TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604800 17514 ENSG00000051128
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NSC5
Protein name Homer protein homolog 3 (Homer-3)
Protein function Postsynaptic density scaffolding protein. Binds and cross-links cytoplasmic regions of GRM1, GRM5, ITPR1, DNM3, RYR1, RYR2, SHANK1 and SHANK3. By physically linking GRM1 and GRM5 with ER-associated ITPR1 receptors, it aids the coupling of surfac
PDB 2P8V , 3CVF
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00568 WH1 1 110 WH1 domain Domain
Sequence
MSTAREQPIFSTRAHVFQIDPATKRNWIPAGKHALTVSYFYDATRNVYRIISIGGAKAII
NSTVTPNMTFTKTSQKFGQWADSRANTVYGLGFASEQHLTQFAEKFQEVK
EAARLAREKS
QDGGELTSPALGLASHQVPPSPLVSANGPGEEKLFRSQSADAPGPTERERLKKMLSEGSV
GEVQWEAEFFALQDSNNKLAGALREANAAAAQWRQQLEAQRAEAERLRQRVAELEAQAAS
EVTPTGEKEGLGQGQSLEQLEALVQTKDQEIQTLKSQTGGPREALEAAEREETQQKVQDL
ETRNAELEHQLRAMERSLEEARAERERARAEVGRAAQLLDVSLFELSELREGLARLAEAA
P
Sequence length 361
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  FoxO signaling pathway
Glutamatergic synapse
  Neurexins and neuroligins
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Keratoconus 5 Uncertain significance rs2513132510 RCV004572866
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Depressive Disorder Major Associate 37511534
Glioma Associate 33885248
Hypoxia Associate 34108014
Keratoconus Associate 39238827
Leukemia Associate 23725168
Leukemia Myeloid Acute Associate 23725168
Mood Disorders Associate 37511534
Neoplasm Metastasis Associate 34108014
Neoplasms Associate 34108014
Precursor T Cell Lymphoblastic Leukemia Lymphoma Associate 37820824