Entity Details

Primary name FSHR_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP23945
EntryNameFSHR_HUMAN
FullNameFollicle-stimulating hormone receptor
TaxID9606
Evidenceevidence at protein level
Length695
SequenceStatuscomplete
DateCreated1992-03-01
DateModified2021-06-02

Ontological Relatives

GenesFSHR

GO terms

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GOName
GO:0002862 negative regulation of inflammatory response to antigenic stimulus
GO:0004963 follicle-stimulating hormone receptor activity
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway
GO:0007190 activation of adenylate cyclase activity
GO:0007283 spermatogenesis
GO:0007292 female gamete generation
GO:0008406 gonad development
GO:0008528 G protein-coupled peptide receptor activity
GO:0008584 male gonad development
GO:0008585 female gonad development
GO:0009755 hormone-mediated signaling pathway
GO:0010738 regulation of protein kinase A signaling
GO:0014068 positive regulation of phosphatidylinositol 3-kinase signaling
GO:0016021 integral component of membrane
GO:0042699 follicle-stimulating hormone signaling pathway
GO:0043235 receptor complex
GO:0070374 positive regulation of ERK1 and ERK2 cascade
GO:0071372 cellular response to follicle-stimulating hormone stimulus

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR000276 G protein-coupled receptor, rhodopsin-likeFamilyFamily
IPR000372 Leucine-rich repeat N-terminal domainDomainDomain
IPR002131 Glycoprotein hormone receptor familyFamilyFamily
IPR002272 Follicle stimulating hormone receptorFamilyFamily
IPR017452 GPCR, rhodopsin-like, 7TMDomainDomain
IPR024635 Gonadotropin hormone receptor, transmembrane domainDomainDomain
IPR026906 BspA type Leucine rich repeat regionRepeatRepeat

Diseases

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Disease IDSourceNameDescription
608115 OMIMOvarian hyperstimulation syndrome (OHSS)Disorder which occurs either spontaneously or most often as an iatrogenic complication of ovarian stimulation treatments for in vitro fertilization. The clinical manifestations vary from abdominal distention and discomfort to potentially life-threatening, massive ovarian enlargement and capillary leak with fluid sequestration. Pathologic features of this syndrome include the presence of multiple serous and hemorrhagic follicular cysts lined by luteinized cells, a condition called hyperreactio luteinalis. The disease is caused by variants affecting the gene represented in this entry.
233300 OMIMOvarian dysgenesis 1 (ODG1)An autosomal recessive disease characterized by primary amenorrhea, variable development of secondary sex characteristics, poorly developed streak ovaries, and high serum levels of follicle-stimulating hormone (FSH) and luteinizing hormone (LH). The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00032 MenotropinsDrugbankbiotech
DB00066 FollitropinDrugbankbiotech
DB00094 UrofollitropinDrugbankbiotech
DB00097 Choriogonadotropin alfaDrugbankbiotech
DB04786 SuraminDrugbanksmall molecule
DB09066 Corifollitropin alfaDrugbankbiotech