Gene Gene information from NCBI Gene database.
Entrez ID 11328
Gene name FKBP prolyl isomerase 9
Gene symbol FKBP9
Synonyms (NCBI Gene)
FKBP60FKBP63PPIase
Chromosome 7
Chromosome location 7p14.3
miRNA miRNA information provided by mirtarbase database.
718
miRTarBase ID miRNA Experiments Reference
MIRT029796 hsa-miR-26b-5p Microarray 19088304
MIRT042868 hsa-miR-324-3p CLASH 23622248
MIRT650422 hsa-miR-548av-3p HITS-CLIP 23824327
MIRT650421 hsa-miR-186-3p HITS-CLIP 23824327
MIRT650420 hsa-miR-6787-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
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:0005509 Function Calcium ion binding IEA
GO:0005509 Function Calcium ion binding ISS
GO:0005783 Component Endoplasmic reticulum IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616257 3725 ENSG00000122642
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95302
Protein name Peptidyl-prolyl cis-trans isomerase FKBP9 (PPIase FKBP9) (EC 5.2.1.8) (63 kDa FK506-binding protein) (63 kDa FKBP) (FKBP-63) (FK506-binding protein 9) (FKBP-9) (Rotamase)
Protein function PPIases accelerate the folding of proteins during protein synthesis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00254 FKBP_C 47 139 FKBP-type peptidyl-prolyl cis-trans isomerase Domain
PF00254 FKBP_C 159 251 FKBP-type peptidyl-prolyl cis-trans isomerase Domain
PF00254 FKBP_C 271 362 FKBP-type peptidyl-prolyl cis-trans isomerase Domain
PF00254 FKBP_C 382 474 FKBP-type peptidyl-prolyl cis-trans isomerase Domain
Sequence
Sequence length 570
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
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
AMYOTROPHIC LATERAL SCLEROSIS 1 Lateral Sclerosis BEFREE 10077670
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 31575382 Associate
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma Pubtator 32620753 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of prostate Prostate cancer BEFREE 31780055
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 31780055
★☆☆☆☆
Found in Text Mining only
Parkinson Disease Parkinson disease BEFREE 31830361
★☆☆☆☆
Found in Text Mining only
Prostate carcinoma Prostate cancer BEFREE 31780055
★☆☆☆☆
Found in Text Mining only
Stomach Diseases Stomach Diseases BEFREE 29148176
★☆☆☆☆
Found in Text Mining only