Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11140
Gene name Gene Name - the full gene name approved by the HGNC.
Cell division cycle 37, HSP90 cochaperone
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CDC37
Synonyms (NCBI Gene) Gene synonyms aliases
P50CDC37
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is highly similar to Cdc 37, a cell division cycle control protein of Sacchromyces cerevisiae. This protein is a molecular chaperone with specific function in cell signal transduction. It has been shown to form complex wit
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016144 hsa-miR-615-3p Sequencing 20371350
MIRT016565 hsa-miR-193b-3p Proteomics 21512034
MIRT025907 hsa-miR-7-5p Microarray 19073608
MIRT031991 hsa-miR-16-5p Sequencing 20371350
MIRT049255 hsa-miR-92a-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000079 Process Regulation of cyclin-dependent protein serine/threonine kinase activity TAS 8666233
GO:0005515 Function Protein binding IPI 9150368, 11036079, 12176997, 14676191, 14743216, 16321986, 17979178, 19026643, 19875381, 20562859, 20642453, 21163940, 21360678, 21871133, 21900206, 21903422, 22612223, 22939624, 23075850, 23428871, 23455922, 24189400, 24366813, 24618592, 24880080, 24981860, 25036637, 25486457, 2649
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005737 Component Cytoplasm IDA
GO:0005829 Component Cytosol IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605065 1735 ENSG00000105401
Protein
UniProt ID Q16543
Protein name Hsp90 co-chaperone Cdc37 (Hsp90 chaperone protein kinase-targeting subunit) (p50Cdc37) [Cleaved into: Hsp90 co-chaperone Cdc37, N-terminally processed]
Protein function Co-chaperone that binds to numerous kinases and promotes their interaction with the Hsp90 complex, resulting in stabilization and promotion of their activity (PubMed:8666233). Inhibits HSP90AA1 ATPase activity (PubMed:23569206). {ECO:0000269|Pub
PDB 1US7 , 2K5B , 2N5X , 2NCA , 2W0G , 5FWK , 5FWL , 5FWM , 5FWP , 5HPE , 7Z37 , 7Z38 , 7ZR0 , 7ZR5 , 7ZR6 , 8GAE , 8GFT , 8U1L
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03234 CDC37_N 1 164 Cdc37 N terminal kinase binding Domain
PF08565 CDC37_M 161 276 Cdc37 Hsp90 binding domain Domain
PF08564 CDC37_C 286 360 Cdc37 C terminal domain Domain
Sequence
Sequence length 378
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  PI3K-Akt signaling pathway   Signaling by ERBB2
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants
Constitutive Signaling by EGFRvIII
Downregulation of ERBB2 signaling
Constitutive Signaling by Overexpressed ERBB2
Drug-mediated inhibition of ERBB2 signaling
Signaling by ERBB2 KD Mutants
Resistance of ERBB2 KD mutants to trastuzumab
Resistance of ERBB2 KD mutants to sapitinib
Resistance of ERBB2 KD mutants to tesevatinib
Resistance of ERBB2 KD mutants to neratinib
Resistance of ERBB2 KD mutants to osimertinib
Resistance of ERBB2 KD mutants to afatinib
Resistance of ERBB2 KD mutants to AEE788
Resistance of ERBB2 KD mutants to lapatinib
Signaling by ERBB2 ECD mutants
Signaling by ERBB2 TMD/JMD mutants
Drug resistance in ERBB2 TMD/JMD mutants
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hypercholesterolemia Hypercholesterolemia, Familial rs28942111, rs28942112, rs137852912, rs121908025, rs28942082, rs28942083, rs121908028, rs121908030, rs28942079, rs28942084, rs121908032, rs387906302, rs387906303, rs121908033, rs121908034
View all (1161 more)
22968135
Inflammatory bowel disease Inflammatory Bowel Diseases rs137853579, rs137853580, rs121909601, rs149491038, rs368287711, rs387907326, rs587777338, rs758439420, rs1329427406, rs1264862631, rs1192830343, rs1373354533, rs1419560997, rs1591263883, rs1989014468 23128233, 26192919, 28067908
Multiple sclerosis Multiple Sclerosis rs104895219, rs483353022, rs483353023, rs483353028, rs483353029, rs483353024, rs483353030, rs3207617, rs483353031, rs483353032, rs483353033, rs483353034, rs483353035, rs483353036, rs483353039
View all (4 more)
21833088
Unknown
Disease term Disease name Evidence References Source
Crohn disease Crohn Disease 28067908, 26192919 ClinVar
Multiple Sclerosis Multiple Sclerosis GWAS
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Ankylosing Spondylitis Ankylosing Spondylitis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 22912728, 24869908, 24927996
Carcinogenesis Associate 22912728
Carcinoma Hepatocellular Associate 34884975
Colorectal Neoplasms Associate 18931700, 24292678, 27391062, 38359495
COVID 19 Associate 35421970, 36571271
Gastrointestinal Stromal Tumors Associate 23584476, 31776458
Hypoxia Associate 38359495
Multiple Myeloma Associate 21871133
Multiple Myeloma Stimulate 37409850
Multiple Sclerosis Associate 36571271