Entity Details

Primary name LIGO1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96FE5
EntryNameLIGO1_HUMAN
FullNameLeucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1
TaxID9606
Evidenceevidence at protein level
Length620
SequenceStatuscomplete
DateCreated2008-04-08
DateModified2021-06-02

Ontological Relatives

GenesLINGO1

GO terms

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GOName
GO:0005154 epidermal growth factor receptor binding
GO:0005615 extracellular space
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
GO:0031012 extracellular matrix
GO:0050771 negative regulation of axonogenesis

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR000372 Leucine-rich repeat N-terminal domainDomainDomain
IPR001611 Leucine-rich repeatRepeatRepeat
IPR003591 Leucine-rich repeat, typical subtypeRepeatRepeat
IPR003598 Immunoglobulin subtype 2DomainDomain
IPR003599 Immunoglobulin subtypeDomainDomain
IPR007110 Immunoglobulin-like domainDomainDomain
IPR013098 Immunoglobulin I-setDomainDomain
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR026906 BspA type Leucine rich repeat regionRepeatRepeat
IPR032675 Leucine-rich repeat domain superfamilyFamilyHomologous superfamily
IPR036179 Immunoglobulin-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
618103 OMIMMental retardation, autosomal recessive 64 (MRT64)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRT64 patients have moderate to severe intellectual disability, delayed motor development, aggressive behavior, and slurred or absent speech. The disease is caused by variants affecting the gene represented in this entry.