CC2D1A

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CC2D1A
Identifiers
Aliases CC2D1A, FREUD-1, Freud-1/Aki1, MRT3, coiled-coil and C2 domain containing 1A
External IDs MGI: 2384831 HomoloGene: 23040 GeneCards: CC2D1A
RNA expression pattern
PBB GE CC2D1A 207083 s at fs.png

PBB GE CC2D1A 58994 at fs.png

PBB GE CC2D1A 221888 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_017721

NM_145970

RefSeq (protein)

NP_060191

NP_666082.2
NP_666082

Location (UCSC) Chr 19: 13.91 – 13.93 Mb Chr 8: 84.13 – 84.15 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Coiled-coil and C2 domain-containing protein 1A is a protein that in humans is encoded by the CC2D1A gene.[3][4][5]


References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ Matsuda A, Suzuki Y, Honda G, Muramatsu S, Matsuzaki O, Nagano Y, Doi T, Shimotohno K, Harada T, Nishida E, Hayashi H, Sugano S (May 2003). "Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways". Oncogene. 22 (21): 3307–18. doi:10.1038/sj.onc.1206406. PMID 12761501. 
  4. ^ Basel-Vanagaite L, Attia R, Yahav M, Ferland RJ, Anteki L, Walsh CA, Olender T, Straussberg R, Magal N, Taub E, Drasinover V, Alkelai A, Bercovich D, Rechavi G, Simon AJ, Shohat M (Mar 2006). "The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non‐syndromic mental retardation". J Med Genet. 43 (3): 203–10. doi:10.1136/jmg.2005.035709. PMC 2563235Freely accessible. PMID 16033914. 
  5. ^ "Entrez Gene: CC2D1A coiled-coil and C2 domain containing 1A". 

External links[edit]

Further reading[edit]