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Gene : CNBP Homo sapiens

Name  ? CCHC-type zinc finger nucleic acid binding protein Cytological Location  3q21.3
Brief Description  CCHC-type zinc finger nucleic acid binding protein
Description  This gene encodes a nucleic-acid binding protein with seven zinc-finger domains. The protein has a preference for binding single stranded DNA and RNA. The protein functions in cap-independent translation of ornithine decarboxylase mRNA, and may also function in sterol-mediated transcriptional regulation. A CCTG expansion from <30 repeats to 75-11000 repeats in the first intron of this gene results in myotonic dystrophy type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2016]
  • synonyms:
  • zinc finger protein 9 (a cellular retroviral nucleic acid binding protein),
  • uc003elq.5,
  • RNF163,
  • NM_003418,
  • ZCCHC22,
  • HGNC:13164,
  • ZNF9,
  • ZNF9,
  • DM2,
  • CNBP1,
  • DM2,
  • RNF163,
  • PROMM,
  • CNBP,
  • OTTHUMG00000159943,
  • U19765,
  • CCHC-type zinc finger, nucleic acid binding protein,
  • CNBP1,
  • ZCCHC22,
  • zinc finger protein 9
  • identifiers:
  • 7555,
  • ENSG00000169714,
  • CNBP

Genome feature

Region: gene ? Length: 16070  
Location: 3:129167827-129183896 reverse strand Cyto location: 3q21.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 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 --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

153 SN Ps

5 Cross References

18 Data Sets

8 Homologues

0 Located Features

97 Rna Seq Results