Homo sapiens Protein: ITGB4
Summary
InnateDB Protein IDBP-68786.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ITGB4
Protein Name integrin, beta 4
Synonyms CD104;
Species Homo sapiens
Ensembl Protein ENSP00000200181
InnateDB Gene IDBG-68784 (ITGB4)
Protein Structure
UniProt Annotation
Function Integrin alpha-6/beta-4 is a receptor for laminin. Plays a critical structural role in the hemidesmosome of epithelial cells. Is required for the regulation of keratinocyte polarity and motility. {ECO:0000269PubMed:12482924, ECO:0000269PubMed:19403692}.
Subcellular Localization Cell membrane; Single-pass type I membrane protein. Cell membrane; Lipid-anchor. Cell junction, hemidesmosome. Note=Colocalizes with DST at the leading edge of migrating keratinocytes.
Disease Associations Epidermolysis bullosa letalis, with pyloric atresia (EB- PA) [MIM:226730]: An autosomal recessive, frequently lethal, epidermolysis bullosa with variable involvement of skin, nails, mucosa, and with variable effects on the digestive system. It is characterized by mucocutaneous fragility, aplasia cutis congenita, and gastrointestinal atresia, which most commonly affects the pylorus. Pyloric atresia is a primary manifestation rather than a scarring process secondary to epidermolysis bullosa. {ECO:0000269PubMed:10873890, ECO:0000269PubMed:11251584, ECO:0000269PubMed:11328943, ECO:0000269PubMed:9422533, ECO:0000269PubMed:9546354, ECO:0000269PubMed:9792864, ECO:0000269PubMed:9892956}. Note=The disease is caused by mutations affecting the gene represented in this entry.Generalized atrophic benign epidermolysis bullosa (GABEB) [MIM:226650]: A non-lethal, adult form of junctional epidermolysis bullosa characterized by life-long blistering of the skin, associated with hair and tooth abnormalities. {ECO:0000269PubMed:10792571}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Integrin alpha-6/beta-4 is predominantly expressed by epithelia. Isoform beta-4D is also expressed in colon and placenta. Isoform beta-4E is also expressed in epidermis, lung, duodenum, heart, spleen and stomach.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 28 experimentally validated interaction(s) in this database.
Experimentally validated
Total 28 [view]
Protein-Protein 28 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0001664 G-protein coupled receptor binding
GO:0004872 receptor activity
GO:0005515 protein binding
Biological Process
GO:0006914 autophagy
GO:0007154 cell communication
GO:0007155 cell adhesion
GO:0007160 cell-matrix adhesion
GO:0007229 integrin-mediated signaling pathway
GO:0007275 multicellular organismal development
GO:0009611 response to wounding
GO:0030198 extracellular matrix organization
GO:0031581 hemidesmosome assembly
GO:0034329 cell junction assembly
GO:0046847 filopodium assembly
GO:0048870 cell motility
Cellular Component
GO:0005604 basement membrane
GO:0005886 plasma membrane
GO:0008305 integrin complex
GO:0009925 basal plasma membrane
GO:0009986 cell surface
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0030056 hemidesmosome
GO:0031252 cell leading edge
GO:0043235 receptor complex
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR002035 von Willebrand factor, type A
IPR002369 Integrin beta subunit, N-terminal
IPR003644 Na-Ca exchanger/integrin-beta4
IPR003961 Fibronectin, type III
IPR012013 Integrin beta-4 subunit
IPR012896 Integrin beta subunit, tail
IPR013111 EGF-like domain, extracellular
IPR015812 Integrin beta subunit
IPR016201 Plexin-like fold
PFAM PF00092
PF00362
PF03160
PF00041
PF01108
PF07965
PF07974
PRINTS PR01186
PIRSF PIRSF002513
PIRSF002512
SMART SM00327
SM00187
SM00237
SM00060
SM00423
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P16144
PhosphoSite PhosphoSite-P16144
TrEMBL A0A024R8T0
UniProt Splice Variant
Entrez Gene 3691
UniGene Hs.632226
RefSeq NP_000204
HUGO HGNC:6158
OMIM 147557
CCDS CCDS11727
HPRD 00946
IMGT
EMBL AC087749 AF011375 AF011376 AJ251004 BC118916 BC126411 CH471099 U66530 U66531 U66532 U66533 U66534 U66535 U66536 U66537 U66538 U66539 U66540 U66541 X51841 X52186 X53587 Y11107
GenPept AAB65421 AAB65422 AAC51632 AAC51633 AAC51634 AAI18917 AAI26412 CAA36134 CAA36433 CAA37656 CAB61345 EAW89305 EAW89312 EAW89315