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Gene : SNX21 Homo sapiens

Name  ? sorting nexin family member 21 Cytological Location  20q13.12
Brief Description  sorting nexin family member 21
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. The specific function of this protein has not been determined. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • dJ337O18.4,
  • uc002xpv.2,
  • PP3993,
  • C20orf161,
  • SNX-L,
  • HGNC:16154,
  • SNX-L,
  • NM_033421,
  • chromosome 20 open reading frame 161,
  • SNX21,
  • dJ337O18.4,
  • OTTHUMG00000032624,
  • C20orf161,
  • AK095851
  • identifiers:
  • 90203,
  • ENSG00000124104,
  • SNX21

Genome feature

Region: gene ? Length: 9858  
Location: 20:45833418-45843275 Cyto location: 20q13.12


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Gene --> Orthologues

Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

2011 SN Ps

4 Cross References

14 Data Sets

5 Homologues

0 Located Features

90 Rna Seq Results