Gene Gene information from NCBI Gene database.
Entrez ID 29916
Gene name Sorting nexin 11
Gene symbol SNX11
Synonyms (NCBI Gene)
-
Chromosome 17
Chromosome location 17q21.32
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
miRNA miRNA information provided by mirtarbase database.
267
miRTarBase ID miRNA Experiments Reference
MIRT045867 hsa-miR-128-3p CLASH 23622248
MIRT042365 hsa-miR-484 CLASH 23622248
MIRT038195 hsa-miR-151a-5p CLASH 23622248
MIRT146496 hsa-miR-15a-5p HITS-CLIP 22473208
MIRT146501 hsa-miR-15b-5p HITS-CLIP 22473208
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 26818531, 32296183
GO:0005737 Component Cytoplasm IDA 26818531
GO:0005737 Component Cytoplasm IEA
GO:0005768 Component Endosome IBA
GO:0005768 Component Endosome IDA 23615901
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614906 14975 ENSG00000002919
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y5W9
Protein name Sorting nexin-11
Protein function Phosphoinositide-binding protein involved in protein sorting and membrane trafficking in endosomes (PubMed:23615901). Regulates the levels of TRPV3 by promoting its trafficking from the cell membrane to lysosome for degradation (PubMed:26818531)
PDB 4IKB , 4IKD , 6KOI , 6KOJ , 6KOK
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00787 PX 46 129 PX domain Domain
Sequence
MGFWCRMSENQEQEEVITVRVQDPRVQNEGSWNSYVDYKIFLHTNSKAFTAKTSCVRRRY
REFVWLRKQLQRNAGLVPVPELPGKSTFFGTSDEFIEKRRQGLQHFLEKVLQSVVLLSDS
QLHLFLQSQ
LSVPEIEACVQGRSTMTVSDAILRYAMSNCGWAQEERQSSSHLAKGDQPKS
CCFLPRSGRRSSPSPPPSEEKDHLEVWAPVVDSEVPSLESPTLPPLSSPLCCDFGRPKEG
TSTLQSVRRAVGGDHAVPLDPGQLETVLEK
Sequence length 270
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANOREXIA NERVOSA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FIBRILLATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ENDOMETRIAL CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ENDOMETRIAL CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Endometrial Neoplasms Endometrial neoplasm Pubtator 39401154 Associate
★☆☆☆☆
Found in Text Mining only