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Gene : NSFL1C Homo sapiens

Name  ? NSFL1 cofactor Cytological Location  20p13
Brief Description  NSFL1 cofactor
Description  N-ethylmaleimide-sensitive factor (NSF) and valosin-containing protein (p97) are two ATPases known to be involved in transport vesicle/target membrane fusion and fusions between membrane compartments. A trimer of the protein encoded by this gene binds a hexamer of cytosolic p97 and is required for p97-mediated regrowth of Golgi cisternae from mitotic Golgi fragments. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 8. [provided by RefSeq, May 2011]
  • synonyms:
  • uc002wfc.3,
  • NSFL1C,
  • UBXD10,
  • UBXN2C,
  • SHP1 homolog (S. cerevisiae),
  • AF112211,
  • UBX domain protein 2C,
  • UBX1,
  • OTTHUMG00000031665,
  • dJ776F14.1,
  • NM_016143,
  • NSFL1 (p97) cofactor (p47),
  • dJ776F14.1,
  • UBXN2C,
  • P47,
  • p47,
  • UBXD10,
  • HGNC:15912,
  • UBX1
  • identifiers:
  • 55968,
  • ENSG00000088833,
  • NSFL1C

Genome feature

Region: gene ? Length: 25632  
Location: 20:1442162-1467793 reverse strand Cyto location: 20p13


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Proteins

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SNPs

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Disease

0 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Expression

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Other

3753 SN Ps

5 Cross References

17 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results