Entity Details

Primary name HMCN1
Entity type gene
Source Source Link

Details

PrimaryID83872
RefseqGeneNG_011841
SymbolHMCN1
Namehemicentin 1
Chromosome1
Location1q25.3-q31.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-06
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsHMCN1_HUMAN

GO terms

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GOName
GO:0005201 extracellular matrix structural constituent
GO:0005509 calcium ion binding
GO:0005604 basement membrane
GO:0005912 adherens junction
GO:0005938 cell cortex
GO:0007049 cell cycle
GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules
GO:0007157 heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules
GO:0007601 visual perception
GO:0009617 response to bacterium
GO:0032154 cleavage furrow
GO:0051301 cell division
GO:0062023 collagen-containing extracellular matrix
GO:0070062 extracellular exosome

Diseases

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Disease IDSourceNameDescription
603075 OMIMMacular degeneration, age-related, 1 (ARMD1)A form of age-related macular degeneration, a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane. The disease is caused by variants affecting the gene represented in this entry.

Interactions

7 interactions