Entity Details

Primary name LSHB_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP01229
EntryNameLSHB_HUMAN
FullNameLutropin subunit beta
TaxID9606
Evidenceevidence at protein level
Length141
SequenceStatuscomplete
DateCreated1986-07-21
DateModified2021-06-02

Ontological Relatives

GenesLHB

GO terms

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GOName
GO:0002862 negative regulation of inflammatory response to antigenic stimulus
GO:0005102 signaling receptor binding
GO:0005179 hormone activity
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0005796 Golgi lumen
GO:0006701 progesterone biosynthetic process
GO:0007165 signal transduction
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007267 cell-cell signaling
GO:0008584 male gonad development
GO:0009755 hormone-mediated signaling pathway
GO:0016486 peptide hormone processing

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR001545 Gonadotropin, beta subunitFamilyFamily
IPR006208 Glycoprotein hormone subunit betaDomainDomain
IPR018245 Gonadotropin, beta subunit, conserved siteSiteConserved site
IPR029034 Cystine-knot cytokineFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
228300 OMIMHypogonadotropic hypogonadism 23 without anosmia (HH23)A form of hypogonadotropic hypogonadism, a group of disorders characterized by absent or incomplete sexual maturation by the age of 18 years, in conjunction with low levels of circulating gonadotropins and testosterone and no other abnormalities of the hypothalamic-pituitary axis. HH23 male patients have normal sexual differentiation, reduced or absent Leydig cells, reduced or absent spermatogenesis, and absence of spontaneous puberty. Female patients exhibit normal pubertal development and menarche, followed by oligomenorrhea and anovulatory secondary amenorrhea. The disease is caused by variants affecting the gene represented in this entry.