CC2D2A

Protein-coding gene in the species Homo sapiens
CC2D2A
Identifiers
AliasesCC2D2A, JBTS9, MKS6, coiled-coil and C2 domain containing 2A, COACH2, RP93
External IDsOMIM: 612013; MGI: 1924487; HomoloGene: 18159; GeneCards: CC2D2A; OMA:CC2D2A - orthologs
Gene location (Human)
Chromosome 4 (human)
Chr.Chromosome 4 (human)[1]
Chromosome 4 (human)
Genomic location for CC2D2A
Genomic location for CC2D2A
Band4p15.32Start15,469,865 bp[1]
End15,601,552 bp[1]
Gene location (Mouse)
Chromosome 5 (mouse)
Chr.Chromosome 5 (mouse)[2]
Chromosome 5 (mouse)
Genomic location for CC2D2A
Genomic location for CC2D2A
Band5|5 B3Start43,662,346 bp[2]
End43,740,972 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right uterine tube

  • bronchial epithelial cell

  • ventricular zone

  • Achilles tendon

  • olfactory zone of nasal mucosa

  • epithelium of colon

  • sural nerve

  • right coronary artery

  • ganglionic eminence

  • popliteal artery
Top expressed in
  • retinal pigment epithelium

  • pituitary gland

  • otolith organ

  • utricle

  • ciliary body

  • iris

  • neural layer of retina

  • autopod region

  • foot

  • hand
More reference expression data
BioGPS
n/a
Orthologs
SpeciesHumanMouse
Entrez

57545

231214

Ensembl

ENSG00000048342

ENSMUSG00000039765

UniProt

Q9P2K1

Q8CFW7

RefSeq (mRNA)

NM_001080522
NM_001164720
NM_020785
NM_001378615
NM_001378617

NM_172274
NM_001359903
NM_001359904
NM_001359905
NM_001359906

RefSeq (protein)

NP_001073991
NP_001158192
NP_065836
NP_001365544
NP_001365546

NP_758478
NP_001346832
NP_001346833
NP_001346834
NP_001346835

Location (UCSC)Chr 4: 15.47 – 15.6 MbChr 5: 43.66 – 43.74 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Coiled-coil and C2 domain-containing protein 2A that in humans is encoded by the CC2D2A gene.[5][6][7]

Function

This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation.[5]

Clinical significance

Mutations in the CC2D2A gene are associated with Meckel syndrome as well as Joubert syndrome.[5]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000048342 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000039765 – Ensembl, 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. ^ a b c "Entrez Gene: coiled-coil and C2 domain containing 2A".
  6. ^ Nagase T, Kikuno R, Ishikawa KI, Hirosawa M, Ohara O (February 2000). "Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro". DNA Res. 7 (1): 65–73. doi:10.1093/dnares/7.1.65. PMID 10718198.
  7. ^ Tallila J, Jakkula E, Peltonen L, Salonen R, Kestilä M (June 2008). "Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle". Am. J. Hum. Genet. 82 (6): 1361–7. doi:10.1016/j.ajhg.2008.05.004. PMC 2427307. PMID 18513680.

External links

Further reading

  • Mougou-Zerelli S, Thomas S, Szenker E, et al. (2009). "CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation". Hum. Mutat. 30 (11): 1574–82. doi:10.1002/humu.21116. PMC 2783384. PMID 19777577.
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
  • Noor A, Windpassinger C, Patel M, et al. (2008). "Addendum. CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa". Am. J. Hum. Genet. 83 (5): 656. doi:10.1016/j.ajhg.2008.10.005. PMC 2674770. PMID 19068953.
  • Dick DM, Aliev F, Krueger RF, et al. (2010). "Genome-wide association study of conduct disorder symptomatology". Molecular Psychiatry. 16 (8): 800–808. doi:10.1038/mp.2010.73. PMC 3580835. PMID 20585324.
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
  • Noor A, Windpassinger C, Patel M, et al. (2008). "CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa". Am. J. Hum. Genet. 82 (4): 1011–8. doi:10.1016/j.ajhg.2008.01.021. PMC 2427291. PMID 18387594.
  • Doherty D, Parisi MA, Finn LS, et al. (2010). "Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)". J. Med. Genet. 47 (1): 8–21. doi:10.1136/jmg.2009.067249. PMC 3501959. PMID 19574260.
  • Gorden NT, Arts HH, Parisi MA, et al. (2008). "CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290". Am. J. Hum. Genet. 83 (5): 559–71. doi:10.1016/j.ajhg.2008.10.002. PMC 2668034. PMID 18950740.

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


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