Entity Details

Primary name HECAM_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ14CZ8
EntryNameHECAM_HUMAN
FullNameHepatocyte cell adhesion molecule
TaxID9606
Evidenceevidence at protein level
Length416
SequenceStatuscomplete
DateCreated2007-08-21
DateModified2021-06-02

Ontological Relatives

GenesHEPACAM

GO terms

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GOName
GO:0005737 cytoplasm
GO:0005911 cell-cell junction
GO:0007155 cell adhesion
GO:0016021 integral component of membrane
GO:0030424 axon
GO:0034613 cellular protein localization
GO:0040008 regulation of growth

Subcellular Location

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Subcellular Location
Cytoplasm
Membrane

Domains

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DomainNameCategoryType
IPR003598 Immunoglobulin subtype 2DomainDomain
IPR003599 Immunoglobulin subtypeDomainDomain
IPR007110 Immunoglobulin-like domainDomainDomain
IPR013106 Immunoglobulin V-set domainDomainDomain
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR036179 Immunoglobulin-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
613926 OMIMLeukoencephalopathy, megalencephalic, with subcortical cysts, 2B (MLC2B)A neurodegenerative disorder characterized by infantile-onset of macrocephaly and mildly delayed motor development associated with white-matter abnormalities on brain magnetic resonance imaging. The phenotype is milder that MLC2A, with better preserved cerebellar white matter and no subcortical cysts outside the temporal region. On follow-up, patients show normal or almost normal motor function. Some patients have normal intelligence, whereas others have a significant cognitive deficiency. The disease is caused by variants affecting the gene represented in this entry.
613925 OMIMLeukoencephalopathy, megalencephalic, with subcortical cysts, 2A (MLC2A)A neurodegenerative disorder characterized by infantile-onset macrocephaly and later onset of motor deterioration, with ataxia and spasticity, seizures, and cognitive decline of variable severity. The brain appears swollen on magnetic resonance imaging with white-matter abnormalities and subcortical cysts, in all stages of the disease. The disease is caused by variants affecting the gene represented in this entry.

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