Homo sapiens Protein: LAMA4 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-95555.7 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | LAMA4 | ||||||||||||||||||
Protein Name | laminin, alpha 4 | ||||||||||||||||||
Synonyms | CMD1JJ; LAMA3; LAMA4*-1; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000374114 | ||||||||||||||||||
InnateDB Gene | IDBG-95551 (LAMA4) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. | ||||||||||||||||||
Subcellular Localization | Secreted, extracellular space, extracellular matrix, basement membrane. Note=Major component. | ||||||||||||||||||
Disease Associations | Cardiomyopathy, dilated 1JJ (CMD1JJ) [MIM:615235]: A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. {ECO:0000269PubMed:17646580}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | In adult, strong expression in heart, lung, ovary small and large intestines, placenta, liver; weak or no expression in skeletal muscle, kidney, pancreas, testis, prostate, brain. High expression in fetal lung and kidney. Expression in fetal and newborn tissues is observed in certain mesenchymal cells in tissues such as smooth muscle and dermis. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 20 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 |
IPR000742
Epidermal growth factor-like domain IPR001791 Laminin G domain IPR002049 EGF-like, laminin IPR005189 Focal adhesion kinase, targeting (FAT) domain IPR008985 Concanavalin A-like lectin/glucanases superfamily IPR009254 Laminin I IPR010307 Laminin domain II |
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PFAM |
PF00008
PF00054 PF02210 PF00053 PF03623 PF06008 PF06009 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00181
SM00210 SM00282 SM00180 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q16363 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q16363 | ||||||||||||||||||
TrEMBL | E5RK79 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 3910 | ||||||||||||||||||
UniGene | Hs.654572 | ||||||||||||||||||
RefSeq | |||||||||||||||||||
HUGO | HGNC:6484 | ||||||||||||||||||
OMIM | 600133 | ||||||||||||||||||
CCDS | CCDS34514 | ||||||||||||||||||
HPRD | 02532 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB210027 AL590106 BC004241 BT006690 S78569 X70904 X76939 X91171 Y14240 Z99289 | ||||||||||||||||||
GenPept | AAB34635 AAH04241 AAP35336 BAE06109 CAA50261 CAA54258 CAA62596 CAA74636 CAI12948 CAI12949 CAI12950 CAI42325 | ||||||||||||||||||