PCDH11X, PCDH11Y (GeneID: 83259) | Homo sapiens
Description: protocadherin 11 Y-linked [Source:HGNC Symbol;Acc:HGNC:15813], protocadherin 11 X-linked [Source:HGNC Symbol;Acc:HGNC:8656]
Synonyms: PCDHY, PCDHX, PCDH-PC, PCDH11, PPP1R119, PCDH22, PCDH-X
Other ID(s): HGNC:8656, HGNC:15813, ENSG00000102290, ENSG00000099715
Protein Accession Numbers: NP_001161833, ENST00000215473, ENST00000373094, ENST00000406881, NP_116753, ENST00000361724, NP_001161835, ENST00000362095, ENST00000298274, ENST00000373097, NP_001161832, NP_116755, ENST00000373088, ENST00000400457, NP_116751, NP_001265548, ENST00000361655, NP_001161834, ENST00000333703, ENST00000373094.1, ENST00000504220, NP_116754, NP_116750, ENST00000395337
Statistics: COSMIC(262) PTM(8)
Post translational modifications (PTM) by Type

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000215473 ENST00000333703 You are here now! ENST00000362095 ENST00000400457 NP_001265548 You are here now! NP_116753 You are here now! NP_116754 NP_116755


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00028 Cadherin Cadherin domain 503-593 CL0159 E-set Homo sapiens
PF00028 Cadherin Cadherin domain 607-696 CL0159 E-set Homo sapiens
PF00028 Cadherin Cadherin domain 286-378 CL0159 E-set Homo sapiens
PF00028 Cadherin Cadherin domain 714-805 CL0159 E-set Homo sapiens
PF00028 Cadherin Cadherin domain 176-272 CL0159 E-set Homo sapiens
PF00028 Cadherin Cadherin domain 398-489 CL0159 E-set Homo sapiens
PF08266 Cadherin_2 Cadherin-like 57-147 CL0159 E-set Homo sapiens
PF08374 Protocadherin Protocadherin 807-1030 Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Prostatic Neoplasms Neoplasms ; Male Urogenital Diseases ; 0.857 0.138
Psychotic Disorders Mental Disorders ; 0.857 0.138
Schizoaffective Disorder Mental Disorders ; 0.857 0.138
Nonorganic psychosis N/A 0.857 0.138
Malignant neoplasm of prostate Neoplasms ; Male Urogenital Diseases ; 0.857 0.138
NO RESULT FOUND
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