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CCDC40 (gene)

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Protein-coding gene in humans
CCDC40
Identifiers
AliasesCCDC40, CILD15, FAP172, coiled-coil domain containing 40, CFAP172
External IDsOMIM: 613799; MGI: 2443893; HomoloGene: 27890; GeneCards: CCDC40; OMA:CCDC40 - orthologs
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)
Chromosome 17 (human)Genomic location for CCDC40Genomic location for CCDC40
Band17q25.3Start80,036,632 bp
End80,100,613 bp
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)
Chromosome 11 (mouse)Genomic location for CCDC40Genomic location for CCDC40
Band11|11 E2Start119,119,398 bp
End119,156,064 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right uterine tube

  • bronchial epithelial cell

  • sural nerve

  • olfactory zone of nasal mucosa

  • left testis

  • tendon of biceps brachii

  • anterior pituitary

  • right testis

  • stromal cell of endometrium

  • left uterine tube
Top expressed in
  • choroidal fissure

  • seminiferous tubule

  • otolith organ

  • olfactory epithelium

  • utricle

  • spermatocyte

  • spermatid

  • choroid plexus of fourth ventricle

  • tail of embryo

  • genital tubercle
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

55036

207607

Ensembl

ENSG00000141519

ENSMUSG00000039963

UniProt

Q4G0X9

Q8BI79

RefSeq (mRNA)

NM_001243342
NM_017950
NM_001330508

NM_175430
NM_001364767

RefSeq (protein)

NP_001230271
NP_001317437
NP_060420

NP_780639
NP_001351696

Location (UCSC)Chr 17: 80.04 – 80.1 MbChr 11: 119.12 – 119.16 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

CCDC40 is the gene in humans that encodes the protein named coiled-coil domain containing 40.

Function

This gene encodes a protein that is necessary for motile cilia function. It functions in correct left-right axis formation by regulating the assembly of the inner dynein arm and the dynein regulatory complexes, which control ciliary beat. Mutations in this gene cause primary ciliary dyskinesia type 15, a disorder due to defects in cilia motility. Alternative splicing results in multiple transcript variants. .

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000141519Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000039963Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Coiled-coil domain containing 40".

Further reading

  • Wang J, Lin J, Chang Y, Li P, Yang Y (August 2010). "MCM3AP, a novel HBV integration site in hepatocellular carcinoma and its implication in hepatocarcinogenesis". Journal of Huazhong University of Science and Technology. 30 (4): 425–9. doi:10.1007/s11596-010-0443-3. PMID 20714864. S2CID 195683753.
  • Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJ, Bird TD, Fong CT, Mefford HC, Smith RJ, Stephens K, Zariwala MA, Knowles MR, Leigh MW (1993). "Primary Ciliary Dyskinesia". PMID 20301301. {{cite journal}}: Cite journal requires |journal= (help)
  • Blanchon S, Legendre M, Copin B, Duquesnoy P, Montantin G, Kott E, Dastot F, Jeanson L, Cachanado M, Rousseau A, Papon JF, Beydon N, Brouard J, Crestani B, Deschildre A, Désir J, Dollfus H, Leheup B, Tamalet A, Thumerelle C, Vojtek AM, Escalier D, Coste A, de Blic J, Clément A, Escudier E, Amselem S (June 2012). "Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia". Journal of Medical Genetics. 49 (6): 410–6. doi:10.1136/jmedgenet-2012-100867. PMID 22693285. S2CID 54524650.
  • Becker-Heck A, Zohn IE, Okabe N, Pollock A, Lenhart KB, Sullivan-Brown J, McSheene J, Loges NT, Olbrich H, Haeffner K, Fliegauf M, Horvath J, Reinhardt R, Nielsen KG, Marthin JK, Baktai G, Anderson KV, Geisler R, Niswander L, Omran H, Burdine RD (January 2011). "The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation". Nature Genetics. 43 (1): 79–84. doi:10.1038/ng.727. PMC 3132183. PMID 21131974.

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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