Homo sapiens Protein: MEGF11
Summary
InnateDB Protein IDBP-239160.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MEGF11
Protein Name multiple EGF-like-domains 11
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000378976
InnateDB Gene IDBG-17824 (MEGF11)
Protein Structure
UniProt Annotation
Function May regulate the mosaic spacing of specific neuron subtypes in the retina through homotypic retinal neuron repulsion. Mosaics provide a mechanism to distribute each cell type evenly across the retina, ensuring that all parts of the visual field have access to a full set of processing elements (By similarity). {ECO:0000250}.
Subcellular Localization Cell membrane {ECO:0000269PubMed:17498693}; Single-pass type I membrane protein {ECO:0000269PubMed:17498693}. Basolateral cell membrane {ECO:0000269PubMed:17498693}; Single- pass type I membrane protein {ECO:0000269PubMed:17498693}. Note=Forms an irregular, mosaic-like adhesion pattern in region of the cell that becomes firmely fixed to the substrate. Localized to protruding lamellipodia. Does not localize with MEGF10.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0010842 retina layer formation
GO:0034109 homotypic cell-cell adhesion
Cellular Component
GO:0016021 integral component of membrane
GO:0016323 basolateral plasma membrane
Protein Structure and Domains
PDB ID
InterPro IPR000742 Epidermal growth factor-like domain
IPR002049 EGF-like, laminin
IPR011489 EMI domain
PFAM PF00008
PF00053
PF07546
PRINTS
PIRSF
SMART SM00181
SM00180
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt A6BM72
PhosphoSite PhosphoSite-A6BM72
TrEMBL C9JYE7
UniProt Splice Variant
Entrez Gene 84465
UniGene Hs.712886
RefSeq XP_006720785
HUGO HGNC:29635
OMIM 612454
CCDS
HPRD 14385
IMGT
EMBL AB058677 AB300051 AC011847 AC084854 AC087382 AL834326 AY358226 BC117419 BC126313
GenPept AAI17420 AAI26314 AAQ88593 BAB47410 BAF64841 CAD38994