Entity Details

Primary name VANG2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9ULK5
EntryNameVANG2_HUMAN
FullNameVang-like protein 2
TaxID9606
Evidenceevidence at protein level
Length521
SequenceStatuscomplete
DateCreated2003-10-31
DateModified2021-06-02

Ontological Relatives

GenesVANGL2

GO terms

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GOName
GO:0001736 establishment of planar polarity
GO:0001843 neural tube closure
GO:0001947 heart looping
GO:0005886 plasma membrane
GO:0005911 cell-cell junction
GO:0016021 integral component of membrane
GO:0016324 apical plasma membrane
GO:0016328 lateral plasma membrane
GO:0035787 cell migration involved in kidney development
GO:0045176 apical protein localization
GO:0060071 Wnt signaling pathway, planar cell polarity pathway
GO:1905515 non-motile cilium assembly

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR009539 Vang-like proteinFamilyFamily

Diseases

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Disease IDSourceNameDescription
182940 OMIMNeural tube defects (NTD)Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy. Failure of neural tube closure can occur at any level of the embryonic axis. Common NTD forms include anencephaly, myelomeningocele and spina bifida, which result from the failure of fusion in the cranial and spinal region of the neural tube. NTDs have a multifactorial etiology encompassing both genetic and environmental components. The disease is caused by variants affecting the gene represented in this entry.