Homo sapiens Gene: SNX7
Summary
InnateDB Gene IDBG-100424.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SNX7
Gene Name sorting nexin 7
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000162627
Encoded Proteins
sorting nexin 7
sorting nexin 7
sorting nexin 7
sorting nexin 7
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region like some family members, and its exact function is unknown. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 11. [provided by RefSeq, Jun 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:98661701-98760500
Strand Forward strand
Band p21.3
Transcripts
ENST00000306121 ENSP00000304429
ENST00000454199 ENSP00000388266
ENST00000473868
ENST00000529992 ENSP00000434731
ENST00000528824 ENSP00000435172
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 11 experimentally validated interaction(s) in this database.
Experimentally validated
Total 11 [view]
Protein-Protein 11 [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
GO:0035091 phosphatidylinositol binding
Biological Process
GO:0006886 intracellular protein transport
GO:0006915 apoptotic process
Cellular Component
GO:0005768 endosome
GO:0030659 cytoplasmic vesicle membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.197015
RefSeq NM_015976 NM_152238
HUGO
OMIM
CCDS CCDS755 CCDS756
HPRD 15416
IMGT
EMBL
GenPept
RNA Seq Atlas