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Gene : CXXC5 Homo sapiens

Name  ? CXXC finger protein 5 Cytological Location  5q31.2
Brief Description  CXXC finger protein 5
Description  The protein encoded by this gene is a retinoid-inducible nuclear protein containing a CXXC-type zinc finger motif. The encoded protein is involved in myelopoiesis, is required for DNA damage-induced p53 activation, regulates the differentiation of C2C12 myoblasts into myocytes, and negatively regulates cutaneous wound healing. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2015]
  • synonyms:
  • CF5,
  • HGNC:26943,
  • uc010jfg.2,
  • WID,
  • CXXC5,
  • HSPC195,
  • WT1-induced Inhibitor of Dishevelled,
  • RINF,
  • AK024338,
  • NM_016463,
  • retinoid-inducible nuclear factor,
  • OTTHUMG00000163331,
  • WID,
  • RINF,
  • HSPC195
  • identifiers:
  • 51523,
  • ENSG00000171604,
  • CXXC5

Genome feature

Region: gene ? Length: 36587  
Location: 5:139647299-139683885 Cyto location: 5q31.2

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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


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]


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



557 SN Ps

5 Cross References

15 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results