Entity Details

Primary name LIPH_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8WWY8
EntryNameLIPH_HUMAN
FullNameLipase member H
TaxID9606
Evidenceevidence at protein level
Length451
SequenceStatuscomplete
DateCreated2007-01-23
DateModified2021-06-02

Ontological Relatives

GenesLIPH

GO terms

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GOName
GO:0004465 lipoprotein lipase activity
GO:0004620 phospholipase activity
GO:0005615 extracellular space
GO:0005886 plasma membrane
GO:0006633 fatty acid biosynthetic process
GO:0006654 phosphatidic acid biosynthetic process
GO:0008201 heparin binding
GO:0016042 lipid catabolic process
GO:0016298 lipase activity
GO:0019433 triglyceride catabolic process

Subcellular Location

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Subcellular Location
Cell membrane
Secreted

Domains

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DomainNameCategoryType
IPR000734 Triacylglycerol lipase familyFamilyFamily
IPR013818 Lipase/vitellogeninDomainDomain
IPR016272 Lipase, LIPH-typeFamilyFamily
IPR029058 Alpha/Beta hydrolase foldFamilyHomologous superfamily
IPR033906 Lipase, N-terminalDomainDomain

Diseases

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Disease IDSourceNameDescription
604379 OMIMHypotrichosis 7 (HYPT7)A condition characterized by the presence of less than the normal amount of hair. Affected individuals have sparse or absent scalp, axillary and body hair and sparse eyebrows and eyelashes. HYPT7 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry.
604379 OMIMHypotrichosis 7 (HYPT7)A condition characterized by the presence of less than the normal amount of hair. Affected individuals have sparse or absent scalp, axillary and body hair and sparse eyebrows and eyelashes. HYPT7 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry.

Interactions

0 interactions

InteractorPartnerSourcesPublicationsLink