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CC2D1A

From Wikipedia, the free encyclopedia

CC2D1A
Identifiers
AliasesCC2D1A,FREUD-1, Freud-1/Aki1, MRT3, coiled-coil and C2 domain containing 1A
External IDsOMIM:610055;MGI:2384831;HomoloGene:23040;GeneCards:CC2D1A;OMA:CC2D1A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_017721

NM_145970
NM_001381871
NM_001381872
NM_001381873

RefSeq (protein)

NP_060191

NP_666082
NP_001368800
NP_001368801
NP_001368802

Location (UCSC)Chr 19: 13.91 – 13.93 MbChr 8: 84.86 – 84.87 Mb
PubMedsearch[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Coiled-coil and C2 domain-containing protein 1Ais aproteinthat in humans is encoded by theCC2D1Agene.[5][6][7]

References

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  1. ^abcGRCh38: Ensembl release 89: ENSG00000132024Ensembl,May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000036686Ensembl,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. ^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.PMID12761501.
  6. ^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.PMC2563235.PMID16033914.
  7. ^"Entrez Gene: CC2D1A coiled-coil and C2 domain containing 1A".
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Further reading

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