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
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.
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.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
HEPACAMC1orf87BioGRID, IntAct28514442 details
HEPACAMKIF23BioGRID31586073 details