Entity Details

Primary name MUC7
Entity type gene
Source Source Link

Details

PrimaryID4589
RefseqGeneNG_012348
SymbolMUC7
Namemucin 7, secreted
Chromosome4
Location4q13.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1995-04-03
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsMUC7_HUMAN

GO terms

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GOName
GO:0002223 stimulatory C-type lectin receptor signaling pathway
GO:0005796 Golgi lumen
GO:0005886 plasma membrane
GO:0016266 O-glycan processing
GO:0031640 killing of cells of other organism
GO:0061844 antimicrobial humoral immune response mediated by antimicrobial peptide
GO:0070062 extracellular exosome

Diseases

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Disease IDSourceNameDescription
600807 OMIMAsthma (ASTHMA)The most common chronic disease affecting children and young adults. It is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment. It is characterized by recurrent attacks of paroxysmal dyspnea, with wheezing due to spasmodic contraction of the bronchi. Disease susceptibility is associated with variants affecting the gene represented in this entry.