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Gene : CCDC39 Homo sapiens

Name  ? coiled-coil domain containing 39 Cytological Location  3q26.33
Brief Description  coiled-coil domain containing 39
Description  The protein encoded by this gene is involved in the motility of cilia and flagella. The encoded protein is essential for the assembly of dynein regulatory and inner dynein arm complexes, which regulate ciliary beat. Defects in this gene are a cause of primary ciliary dyskinesia type 14 (CILD14). [provided by RefSeq, Jul 2011]
  • synonyms:
  • NM_181426,
  • CILD14,
  • HGNC:25244,
  • FAP59,
  • CFAP59,
  • DKFZp434A128,
  • CILD14,
  • OTTHUMG00000157857,
  • CFAP59,
  • uc010hxe.4,
  • FAP59,
  • BC047103,
  • CCDC39
  • identifiers:
  • 339829,
  • ENSG00000284862,
  • CCDC39

Genome feature

Region: gene ? Length: 65482  
Location: 3:180614008-180679489 reverse strand Cyto location: 3q26.33

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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

0 SNPs

5 Cross References

14 Data Sets

3 Homologues

0 Located Features

43 Rna Seq Results