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Gene Gene information from NCBI Gene database.
Entrez ID 642489
Gene name FKBP prolyl isomerase family member 1C
Gene symbol FKBP1C
Synonyms (NCBI Gene)
-
Chromosome 6
Chromosome location 6q12
miRNA miRNA information provided by mirtarbase database.
50 Show/Hide all (50)
miRTarBase ID miRNA Experiments Reference
MIRT498154 hsa-miR-543 PAR-CLIP 21572407
MIRT498153 hsa-miR-541-5p PAR-CLIP 21572407
MIRT498152 hsa-miR-181a-5p PAR-CLIP 21572407
MIRT498151 hsa-miR-181b-5p PAR-CLIP 21572407
MIRT498150 hsa-miR-181c-5p PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6 Show/Hide all (6)
GO ID Ontology Definition Evidence Reference
GO:0003755 Function Peptidyl-prolyl cis-trans isomerase activity IBA
GO:0003755 Function Peptidyl-prolyl cis-trans isomerase activity IEA
GO:0006457 Process Protein folding IBA
GO:0010881 Process Regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion IBA
GO:0016853 Function Isomerase activity 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.
Q5VVH2
Protein name Peptidyl-prolyl cis-trans isomerase FKBP1C (EC 5.2.1.8)
Protein function Catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides.
Family and domains
Sequence
Sequence length
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
14
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.
Show/Hide Unknown Diseases (14)
Phenotype Name Clinical Significance Source Reference Evidence Score
ALZHEIMER DISEASE — GWAS catalog 35589863
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CENTRAL NERVOUS SYSTEM CANCER — GWAS catalog 36810956
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLAUCOMA — GWAS catalog 37601966
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLIOBLASTOMA MULTIFORME — GWAS catalog 36810956
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLIOMA — GWAS catalog 36810956
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations