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Gene : NCF1C Homo sapiens

Name  ? neutrophil cytosolic factor 1C pseudogene Cytological Location  7q11.23
Description  The neutrophil cytosolic factor 1 (NCF1) gene encodes the 47 kDa cytosolic subunit of neutrophil NADPH oxidase, which produces superoxide anion. The NCF1 gene is located in close proximity to two highly similar, multi-exon pseudogenes at chromosome 7q11.23, corresponding to this gene record and GeneID:654816. The two pseudogenes contain a dinucleotide deletion (delta-GT) in exon 2 that results in a frameshift and truncation of the open reading frame, and neither pseudogene is likely to express a protein. Recombination events between the pseudogenes and the functional NCF1 gene can inactivate the NCF1 gene and result in chronic granulomatous disease. [provided by RefSeq, Nov 2009]
  • synonyms:
  • OTTHUMG00000149964,
  • SH3PXD1C,
  • SH3PXD1C,
  • neutrophil cytosolic factor 1C,
  • NR_003187,
  • HGNC:32523
  • identifiers:
  • 654817,
  • ENSG00000165178,
  • NCF1C

Genome feature

Region: gene ?
Location: No location information in HumanMine Cyto location: 7q11.23

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0 Diseases

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

Gene --> Alleles and Disease (clinVar data)

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Mouse Gene --> Allele [Phenotype]


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0 Pathways

967 SN Ps

3 Cross References

8 Data Sets

4 Homologues

0 Located Features

54 Rna Seq Results