Homo sapiens Protein: MUC5B | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-602497.3 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | MUC5B | ||||||||||||||||||
Protein Name | mucin 5B, oligomeric mucus/gel-forming | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000436812 | ||||||||||||||||||
InnateDB Gene | IDBG-18918 (MUC5B) | ||||||||||||||||||
Protein Structure | |||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Gel-forming mucin that is thought to contribute to the lubricating and viscoelastic properties of whole saliva and cervical mucus. | ||||||||||||||||||
Subcellular Localization | Secreted. | ||||||||||||||||||
Disease Associations | Pulmonary fibrosis, idiopathic (IPF) [MIM:178500]: A lung disease characterized by shortness of breath, radiographically evident diffuse pulmonary infiltrates, and varying degrees of inflammation and fibrosis on biopsy. In some cases, the disorder can be rapidly progressive and characterized by sequential acute lung injury with subsequent scarring and end-stage lung disease. {ECO:0000269PubMed:21506741, ECO:0000269PubMed:21506748}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry. A common polymorphism in the promoter of MUC5B is associated with familial interstitial pneumonia and idiopathic pulmonary fibrosis, suggesting that dysregulated MUC5B expression in the lung may be involved in the pathogenesis of pulmonary fibrosis (PubMed:21506741). {ECO:0000269PubMed:21506741}. | ||||||||||||||||||
Tissue Specificity | Expressed on surface airway epithelia. Expressed mainly in mucous cells of submucosal glands of airway tissues. Highly expressed in the sublingual gland. Also found in submaxillary glands, endocervix, gall bladder, and pancreas. {ECO:0000269PubMed:11713095, ECO:0000269PubMed:8554565, ECO:0000269PubMed:9147051, ECO:0000269PubMed:9164870}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR001007
von Willebrand factor, type C IPR001846 von Willebrand factor, type D domain IPR002919 Trypsin Inhibitor-like, cysteine rich domain IPR006207 Cystine knot, C-terminal IPR006552 VWC out IPR014853 Uncharacterised domain, cysteine-rich IPR029034 Cystine-knot cytokine |
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PFAM |
PF00093
PF00094 PF01826 PF08742 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00214
SM00216 SM00041 SM00215 SM00832 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q9HC84 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q9HC84 | ||||||||||||||||||
TrEMBL | Q93043 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 727897 | ||||||||||||||||||
UniGene | Hs.523395 | ||||||||||||||||||
RefSeq | NP_002449 | ||||||||||||||||||
HUGO | HGNC:7516 | ||||||||||||||||||
OMIM | 600770 | ||||||||||||||||||
CCDS | CCDS44515 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AC061979 AF086604 AF107890 AH006676 AJ004862 S80993 U63836 U78551 U95031 X74955 Y09788 Z72496 | ||||||||||||||||||
GenPept | AAB35930 AAB61398 AAB65151 AAC51343 AAC51344 AAC67545 AAG33673 CAA06167 CAA52910 CAA70926 CAA96577 | ||||||||||||||||||