Entity Details

Primary name XPR1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9UBH6
EntryNameXPR1_HUMAN
FullNameXenotropic and polytropic retrovirus receptor 1
TaxID9606
Evidenceevidence at protein level
Length696
SequenceStatuscomplete
DateCreated2008-02-05
DateModified2021-06-02

Ontological Relatives

GenesXPR1

GO terms

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GOName
GO:0000822 inositol hexakisphosphate binding
GO:0001618 virus receptor activity
GO:0004888 transmembrane signaling receptor activity
GO:0004930 G protein-coupled receptor activity
GO:0005737 cytoplasm
GO:0005794 Golgi apparatus
GO:0005886 plasma membrane
GO:0006817 phosphate ion transport
GO:0007186 G protein-coupled receptor signaling pathway
GO:0009615 response to virus
GO:0015114 phosphate ion transmembrane transporter activity
GO:0015562 efflux transmembrane transporter activity
GO:0016021 integral component of membrane
GO:0016036 cellular response to phosphate starvation
GO:0030643 cellular phosphate ion homeostasis
GO:0031226 intrinsic component of plasma membrane
GO:0035435 phosphate ion transmembrane transport
GO:0038023 signaling receptor activity

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR004331 SPX domainDomainDomain
IPR004342 EXS, C-terminalDomainDomain

Diseases

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Disease IDSourceNameDescription
616413 OMIMBasal ganglia calcification, idiopathic, 6 (IBGC6)A form of basal ganglia calcification, an autosomal dominant condition characterized by symmetric calcification in the basal ganglia and other brain regions. Affected individuals can either be asymptomatic or show a wide spectrum of neuropsychiatric symptoms, including parkinsonism, dystonia, tremor, ataxia, dementia, psychosis, seizures, and chronic headache. Serum levels of calcium, phosphate, alkaline phosphatase and parathyroid hormone are normal. The neuropathological hallmark of the disease is vascular and pericapillary calcification, mainly of calcium phosphate, in the affected brain areas. The disease is caused by variants affecting the gene represented in this entry.

Interactions

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