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Gene : SNX18 Homo sapiens

Name  ? sorting nexin 18 Cytological Location  5q11.2
Brief Description  sorting nexin 18
Description  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, but contains a SH3 domain. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • HGNC:19245,
  • AF395536,
  • SH3PXD3B,
  • SH3PX2,
  • SNAG1,
  • SH3PX2,
  • SH3PXD3B,
  • uc003jpi.5,
  • NM_001102575,
  • sorting nexin associated golgi protein 1,
  • SNAG1,
  • OTTHUMG00000096994,
  • SNX18
  • identifiers:
  • 112574,
  • ENSG00000178996,
  • SNX18

Genome feature

Region: gene ? Length: 101491  
Location: 5:54517759-54619249 Cyto location: 5q11.2

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Gene -> HPO annotation (Human Phenotype Ontology)

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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

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Gene --> GO terms.



3756 SN Ps

4 Cross References

14 Data Sets

8 Homologues

0 Located Features

97 Rna Seq Results