Entity Details

Primary name LAMC3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9Y6N6
EntryNameLAMC3_HUMAN
FullNameLaminin subunit gamma-3
TaxID9606
Evidenceevidence at transcript level
Length1575
SequenceStatuscomplete
DateCreated2001-12-13
DateModified2021-06-02

Ontological Relatives

GenesLAMC3

GO terms

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GOName
GO:0005198 structural molecule activity
GO:0005576 extracellular region
GO:0005604 basement membrane
GO:0007601 visual perception
GO:0009887 animal organ morphogenesis
GO:0009888 tissue development
GO:0014002 astrocyte development
GO:0016020 membrane
GO:0016477 cell migration
GO:0030198 extracellular matrix organization
GO:0031012 extracellular matrix
GO:0034446 substrate adhesion-dependent cell spreading
GO:0060041 retina development in camera-type eye

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR000034 Laminin IVDomainDomain
IPR000742 EGF-like domainDomainDomain
IPR002049 Laminin EGF domainDomainDomain
IPR008211 Laminin, N-terminalDomainDomain

Diseases

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Disease IDSourceNameDescription
614115 OMIMCortical malformations occipital (OCCM)A disease in which affected individuals develop seizures, sometimes associated with transient visual changes. Brain MRI shows both pachygyria and polymicrogyria restricted to the lateral occipital lobes. The disease is caused by variants affecting the gene represented in this entry.