Entity Details

Primary name LPAR6_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP43657
EntryNameLPAR6_HUMAN
FullNameLysophosphatidic acid receptor 6
TaxID9606
Evidenceevidence at protein level
Length344
SequenceStatuscomplete
DateCreated1995-11-01
DateModified2021-06-02

Ontological Relatives

GenesLPAR6

GO terms

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GOName
GO:0001835 blastocyst hatching
GO:0004930 G protein-coupled receptor activity
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0007186 G protein-coupled receptor signaling pathway
GO:0035025 positive regulation of Rho protein signal transduction
GO:0051482 positive regulation of cytosolic calcium ion concentration involved in phospholipase C-activating G protein-coupled signaling pathway
GO:0070915 lysophosphatidic acid receptor activity

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR000276 G protein-coupled receptor, rhodopsin-likeFamilyFamily
IPR017452 GPCR, rhodopsin-like, 7TMDomainDomain

Diseases

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Disease IDSourceNameDescription
278150 OMIMWoolly hair autosomal recessive 1 with or without hypotrichosis (ARWH1)A hair shaft disorder characterized by fine and tightly curled hair. Compared to normal curly hair that is observed in some populations, woolly hair grows slowly and stops growing after a few inches. Under light microscopy, woolly hair shows some structural anomalies, including trichorrhexis nodosa and tapered ends. Some individuals exhibit features of hypotrichosis. The disease is caused by variants affecting the gene represented in this entry.
278150 OMIMWoolly hair autosomal recessive 1 with or without hypotrichosis (ARWH1)A hair shaft disorder characterized by fine and tightly curled hair. Compared to normal curly hair that is observed in some populations, woolly hair grows slowly and stops growing after a few inches. Under light microscopy, woolly hair shows some structural anomalies, including trichorrhexis nodosa and tapered ends. Some individuals exhibit features of hypotrichosis. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB01069 PromethazineDrugbanksmall molecule

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
LPAR6_HUMANSMIM3_HUMANBioGRID, IntAct32296183 details
LPAR6_HUMANSC22A_HUMANBioGRID, IntAct32296183 details
LPAR6_HUMANRPRM_HUMANBioGRID, IntAct32296183 details
LPAR6_HUMANEMP1_HUMANBioGRID, IntAct32296183 details