Gene Gene information from NCBI Gene database.
Entrez ID 57658
Gene name Calcium binding and coiled-coil domain 1
Gene symbol CALCOCO1
Synonyms (NCBI Gene)
CocoaPP13275calphoglin
Chromosome 12
Chromosome location 12q13.13
miRNA miRNA information provided by mirtarbase database.
88
miRTarBase ID miRNA Experiments Reference
MIRT858816 hsa-miR-3074-3p CLIP-seq
MIRT858817 hsa-miR-3134 CLIP-seq
MIRT858818 hsa-miR-3201 CLIP-seq
MIRT858819 hsa-miR-3605-5p CLIP-seq
MIRT858820 hsa-miR-3616-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
27
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IEA
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA 24245781
GO:0003682 Function Chromatin binding IEA
GO:0003712 Function Transcription coregulator activity IDA 16344550
GO:0003713 Function Transcription coactivator activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P1Z2
Protein name Calcium-binding and coiled-coil domain-containing protein 1 (Calphoglin) (Coiled-coil coactivator protein) (Sarcoma antigen NY-SAR-3)
Protein function Functions as a coactivator for aryl hydrocarbon and nuclear receptors (NR). Recruited to promoters through its contact with the N-terminal basic helix-loop-helix-Per-Arnt-Sim (PAS) domain of transcription factors or coactivators, such as NCOA2.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17751 SKICH 15 118 SKICH domain Domain
PF07888 CALCOCO1 122 596 Calcium binding and coiled-coil domain (CALCOCO1) like Coiled-coil
PF18112 Zn-C2H2_12 654 680 Autophagy receptor zinc finger-C2H2 domain Domain
Sequence
Sequence length 691
Interactions View interactions
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
EBV-positive nodal T- and NK-cell lymphoma Likely benign rs900627188 RCV004558096
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 19183483
Dyskinesia Drug Induced Associate 34103471
Glioma Associate 31953347
Neoplasms Associate 21542898
Schizophrenia Associate 34103471