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Gene : CISD2 Homo sapiens

Name  ? CDGSH iron sulfur domain 2 Cytological Location  4q24
Brief Description  CDGSH iron sulfur domain 2
description  The protein encoded by this gene is a zinc finger protein that localizes to the endoplasmic reticulum. The encoded protein binds an iron/sulfur cluster and may be involved in calcium homeostasis. Defects in this gene are a cause of Wolfram syndrome 2. [provided by RefSeq, Mar 2011]
  • synonyms:
  • nutrient-deprivation autophagy factor-1,
  • WFS2,
  • ERIS,
  • ZCD2,
  • uc003hwt.5,
  • ERIS,
  • mitoNEET related 1,
  • HGNC:24212,
  • BX537971,
  • ZCD2,
  • zinc finger, CDGSH-type domain 2,
  • Miner1,
  • endoplasmic reticulum intermembrane small protein,
  • WFS2,
  • NAF-1,
  • OTTHUMG00000161014,
  • NAF-1,
  • NM_001008388,
  • Wolfram syndrome 2,
  • CISD2,
  • Miner1
  • identifiers:
  • 493856,
  • ENSG00000145354,
  • CISD2

Genome feature

Region: gene ? Length: 23830  
Location: 4:102868978-102892807 Cyto location: 4q24


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Function

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0 Pathways

Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

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Disease

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

2011 SN Ps

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results