Entity Details

Primary name HEPACAM
Entity type gene
Source Source Link

Details

PrimaryID220296
RefseqGeneNG_029603
SymbolHEPACAM
Namehepatic and glial cell adhesion molecule
Chromosome11
Location11q24.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-05-05
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsHECAM_HUMAN

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

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.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
HEPACAMC1orf87BioGRID, IntAct28514442 details
HEPACAMKIF23BioGRID31586073 details