Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57575
Gene name Gene Name - the full gene name approved by the HGNC.
Protocadherin 10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PCDH10
Synonyms (NCBI Gene) Gene synonyms aliases
OL-PCDH, PCDH19
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q28.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. This family member contains 6 extracellular cadherin domains, a transmembrane domain and a cytoplasmic tail differing from those of the classical cadherins. The e
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT045051 hsa-miR-186-5p CLASH 23622248
MIRT519003 hsa-miR-223-5p HITS-CLIP 21572407
MIRT519002 hsa-miR-6867-5p HITS-CLIP 21572407
MIRT519001 hsa-miR-190a-3p HITS-CLIP 21572407
MIRT552018 hsa-miR-3924 HITS-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding IEA
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0007155 Process Cell adhesion IBA 21873635
GO:0007156 Process Homophilic cell adhesion via plasma membrane adhesion molecules IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608286 13404 ENSG00000138650
Protein
UniProt ID Q9P2E7
Protein name Protocadherin-10
Protein function Potential calcium-dependent cell-adhesion protein.; (Microbial infection) Acts as a receptor for Western equine encephalitis virus.
PDB 6VFQ , 6VFW , 6VG4
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08266 Cadherin_2 19 101 Cadherin-like Domain
PF00028 Cadherin 127 241 Cadherin domain Domain
PF00028 Cadherin 255 349 Cadherin domain Domain
PF00028 Cadherin 364 454 Cadherin domain Domain
PF00028 Cadherin 468 565 Cadherin domain Domain
PF00028 Cadherin 589 679 Cadherin domain Domain
PF16492 Cadherin_C_2 713 838 Cadherin cytoplasmic C-terminal Family
Tissue specificity TISSUE SPECIFICITY: Moderately expressed in all regions of the brain examined, as well as in testis and ovary, and low expression in all other tissues tested. {ECO:0000269|PubMed:11549318}.
Sequence
MIVLLLFALLWMVEGVFSQLHYTVQEEQEHGTFVGNIAEDLGLDITKLSARGFQTVPNSR
TPYLDLNLETGVLYVNEKIDREQICKQSPSCVLHLEVFLEN
PLELFQVEIEVLDINDNPP
SFPEPDLTVEISESATPGTRFPLESAFDPDVGTNSLRDYEITPNSYFSLDVQTQGDGNRF
AELVLEKPLDREQQAVHRYVLTAVDGGGGGGVGEGGGGGGGAGLPPQQQRTGTALLTIRV
L
DSNDNVPAFDQPVYTVSLPENSPPGTLVIQLNATDPDEGQNGEVVYSFSSHISPRAREL
FGLSPRTGRLEVSGELDYEESPVYQVYVQAKDLGPNAVPAHCKVLVRVL
DANDNAPEISF
STVKEAVSEGAAPGTVVALFSVTDRDSEENGQVQCELLGDVPFRLKSSFKNYYTIVTEAP
LDREAGDSYTLTVVARDRGEPALSTSKSIQVQVS
DVNDNAPRFSQPVYDVYVTENNVPGA
YIYAVSATDRDEGANAQLAYSILECQIQGMSVFTYVSINSENGYLYALRSFDYEQLKDFS
FQVEARDAGSPQALAGNATVNILIV
DQNDNAPAIVAPLPGRNGTPAREVLPRSAEPGYLL
TRVAAVDADDGENARLTYSIVRGNEMNLFRMDWRTGELRTARRVPAKRDPQRPYELVIEV
RDHGQPPLSSTATLVVQLV
DGAVEPQGGGGSGGGGSGEHQRPSRSGGGETSLDLTLILII
ALGSVSFIFLLAMIVLAVRCQKEKKLNIYTCLASDCCLCCCCCGGGGSTCCGRQARARKK
KLSKSDIMLVQSSNVPSNPAQVPIEESGGFGSHHHNQNYCYQVCLTPESAKTDLMFLK
PC
SPSRSTDTEHNPCGAIVTGYTDQQPDIISNGSILSNETKHQRAELSYLVDRPRRVNSSAF
QEADIVSSKDSGHGDSEQGDSDHDATNRAQSAGMDLFSNCTEECKALGHSDRCWMPSFVP
SDGRQAADYRSNLHVPGMDSVPDTEVFETPEAQPGAERSFSTFGKEKALHSTLERKELDG
LLTNTRAPYKPPYLTRKRIC
Sequence length 1040
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autism Autistic Disorder rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
18621663
Unknown
Disease term Disease name Evidence References Source
Hypertension Hypertension GWAS
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Prostate cancer Prostate cancer Together, these results show that PRRX2 is an oncogene and might play a role in the aggressiveness of PC within the DNPC population. GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 36461127
Adenoma Associate 27896617
Breast Neoplasms Inhibit 33899544
Burkitt Lymphoma Associate 17341268
Carcinogenesis Associate 19709077
Carcinoma Hepatocellular Inhibit 28498423
Carcinoma Hepatocellular Associate 30170418
Carcinoma in Situ Associate 19709077
Carcinoma Non Small Cell Lung Associate 23321465, 26276761, 36461127
Carcinoma Pancreatic Ductal Associate 31088413