Entity Details

Primary name PTPRQ_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9UMZ3
EntryNamePTPRQ_HUMAN
FullNamePhosphatidylinositol phosphatase PTPRQ
TaxID9606
Evidenceevidence at protein level
Length2332
SequenceStatuscomplete
DateCreated2007-09-11
DateModified2021-06-02

Ontological Relatives

GO terms

Show/Hide Table
GOName
GO:0004725 protein tyrosine phosphatase activity
GO:0016021 integral component of membrane
GO:0043235 receptor complex
GO:0045598 regulation of fat cell differentiation
GO:1990264 peptidyl-tyrosine dephosphorylation involved in inactivation of protein kinase activity

Subcellular Location

Show/Hide Table
Subcellular Location
Membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR000242 PTP type protein phosphataseDomainDomain
IPR000387 Tyrosine specific protein phosphatases domainDomainDomain
IPR003595 Protein-tyrosine phosphatase, catalyticDomainDomain
IPR003961 Fibronectin type IIIDomainDomain
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR016130 Protein-tyrosine phosphatase, active siteSiteActive site
IPR029021 Protein-tyrosine phosphatase-likeFamilyHomologous superfamily
IPR036116 Fibronectin type III superfamilyFamilyHomologous superfamily
IPR041201 PTPRJ, transmembrane domainDomainDomain

Diseases

Show/Hide Table
Disease IDSourceNameDescription
613391 OMIMDeafness, autosomal recessive, 84A (DFNB84A)A form of non-syndromic deafness characterized by progressive, sensorineural hearing loss and vestibular dysfunction. The disease is caused by variants affecting the gene represented in this entry.
617663 OMIMDeafness, autosomal dominant, 73 (DFNA73)A form of non-syndromic hearing loss characterized by mild to severe bilateral symptoms with variable age of onset from early childhood to the third decade. The disease may be caused by variants affecting the gene represented in this entry.