Entity Details

Primary name MUC7_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8TAX7
EntryNameMUC7_HUMAN
FullNameMucin-7
TaxID9606
Evidenceevidence at protein level
Length377
SequenceStatuscomplete
DateCreated2006-05-30
DateModified2021-06-02

Ontological Relatives

GenesMUC7

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

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR033529 Mucin-7FamilyFamily

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.