Homo sapiens Gene: MEGF11
Summary
InnateDB Gene IDBG-17824.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MEGF11
Gene Name multiple EGF-like-domains 11
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000157890
Encoded Proteins
multiple EGF-like-domains 11
multiple EGF-like-domains 11
multiple EGF-like-domains 11
multiple EGF-like-domains 11
multiple EGF-like-domains 11
multiple EGF-like-domains 11
multiple EGF-like-domains 11
multiple EGF-like-domains 11
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 15:65895079-66253747
Strand Reverse strand
Band q22.31
Transcripts
ENST00000288745 ENSP00000288745
ENST00000395614 ENSP00000378976
ENST00000409699 ENSP00000386908
ENST00000422354 ENSP00000414475
ENST00000455812 ENSP00000401400
ENST00000478721
ENST00000490495 ENSP00000456118
ENST00000489275 ENSP00000478311
ENST00000493192
ENST00000478590
ENST00000484618
ENST00000474398
ENST00000469917
ENST00000562154 ENSP00000483007
ENST00000564573 ENSP00000477691
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
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene 84465
UniGene
RefSeq NM_032445
HUGO HGNC:29635
OMIM 612454
CCDS CCDS10213
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas 84465