Gene Gene information from NCBI Gene database.
Entrez ID 84331
Gene name MAPK regulated corepressor interacting protein 2
Gene symbol MCRIP2
Synonyms (NCBI Gene)
C16orf14FAM195Ac349E10.1
Chromosome 16
Chromosome location 16p13.3
miRNA miRNA information provided by mirtarbase database.
91
miRTarBase ID miRNA Experiments Reference
MIRT284923 hsa-miR-6507-3p PAR-CLIP 20371350
MIRT195612 hsa-miR-18a-5p PAR-CLIP 20371350
MIRT195615 hsa-miR-18b-5p PAR-CLIP 20371350
MIRT195622 hsa-miR-4735-3p PAR-CLIP 20371350
MIRT195623 hsa-miR-5584-5p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding IEA
GO:0005515 Function Protein binding IPI 26184334
GO:0005634 Component Nucleus IDA 26184334
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus IEA
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.
Q9BUT9
Protein name MAPK regulated corepressor interacting protein 2 (Protein FAM195A)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14799 FAM195 61 157 FAM195 family Family
Sequence
Sequence length 160
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations