Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9456
Gene name Gene Name - the full gene name approved by the HGNC.
Homer scaffold protein 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HOMER1
Synonyms (NCBI Gene) Gene synonyms aliases
HOMER, HOMER1A, HOMER1B, HOMER1C, SYN47, Ves-1
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q14.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the homer family of dendritic proteins. Members of this family regulate group 1 metabotrophic glutamate receptor function. [provided by RefSeq, Jul 2008]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT032118 hsa-let-7d-5p Sequencing 20371350
MIRT042276 hsa-miR-484 CLASH 23622248
MIRT614961 hsa-miR-19a-3p HITS-CLIP 23824327
MIRT614960 hsa-miR-19b-3p HITS-CLIP 23824327
MIRT614959 hsa-miR-6074 HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003009 Process Skeletal muscle contraction IEA
GO:0005515 Function Protein binding IPI 16189514, 18218901, 19447967, 25416956, 28514442, 32296183, 32814053
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005829 Component Cytosol TAS
GO:0005886 Component Plasma membrane IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604798 17512 ENSG00000152413
Protein
UniProt ID Q86YM7
Protein name Homer protein homolog 1 (Homer-1)
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
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00568 WH1 1 107 WH1 domain Domain
Sequence
MGEQPIFSTRAHVFQIDPNTKKNWVPTSKHAVTVSYFYDSTRNVYRIISLDGSKAIINST
ITPNMTFTKTSQKFGQWADSRANTVYGLGFSSEHHLSKFAEKFQEFK
EAARLAKEKSQEK
MELTSTPSQESAGGDLQSPLTPESINGTDDERTPDVTQNSEPRAEPTQNALPFSHSSAIS
KHWEAELATLKGNNAKLTAALLESTANVKQWKQQLAAYQEEAERLHKRVTELECVSSQAN
AVHTHKTELNQTIQELEETLKLKEEEIERLKQEIDNARELQEQRDSLTQKLQEVEIRNKD
LEGQLSDLEQRLEKSQNEQEAFRNNLKTLLEILDGKIFELTELRDNLAKLLECS
Sequence length 354
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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
12815733, 17317002, 16354916, 16011574
Unknown
Disease term Disease name Evidence References Source
Mental depression Mental Depression, Depressive disorder, Unipolar Depression, Major Depressive Disorder 22267161, 20673876, 22072696 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 32142100, 34502114, 36039594
Atherosclerosis Stimulate 27832625
Autistic Disorder Associate 22558107
Bipolar Disorder Inhibit 25956630
Bipolar Disorder Associate 30178121
Carcinoma Hepatocellular Associate 31790363, 40302343
Cerebral Infarction Associate 27832625
Cholangiocarcinoma Associate 24815486
Cognition Disorders Associate 36039594
Coronary Artery Disease Associate 25551602