ABCMdb

PMID: 15800013

Asheuer M, Bieche I, Laurendeau I, Moser A, Hainque B, Vidaud M, Aubourg P
Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy.
Hum Mol Genet. 2005 May 15;14(10):1293-303. Epub 2005 Mar 30., [PubMed]

Sentences

No. Mutations Sentence Comment

76 ABCD1 p.Tyr174Cys ABCD1 p.Arg464* ABCD1 p.Arg464* ABCD1 p.Trp137* ABCD1 p.Gln177* ABCD1 p.Gln177* ABCD1 p.Gln177* ABCD1 p.Tyr296Cys ABCD1 p.Gly266Arg ABCD1 p.Arg554His ABCD1 p.Arg554His ABCD1 p.Arg554His ABCD1 p.Arg554His ABCD1 p.Glu609Lys ABCD1 p.His667Asp ABCD1 p.His667Asp ABCD1 p.Arg617His ABCD1 p.Leu654Pro ABCD1 p.Leu322Pro ABCD1 p.Ser108Leu ABCD1 p.Ser108Leu ABCD1 p.Arg104Cys ABCD1 p.Arg104Cys ABCD1 p.Arg389Cys ABCD1 p.Arg389Cys ABCD1 p.Gly608Ser ABCD1 p.Gln307* ABCD1 p.Gln307* ABCD1 p.Gln307* ABCD1 p.Tyr666Ser ABCD1 p.Tyr666Ser Mutation Amino acid alteration Type of mutation at the protein level Tissue sample CCER1 521A.G Y174C Missense CCER2 1414insC fsE471 Frame shift CCER3 Unknown Unknown Unknown Fibroblast CCER4 411G.A W137X Nonsense CCER5 1961T.C L654P Missense CCER6 529C.T Q177X Nonsense CCER7 901-1G.A fsE300 Frame shift CCER8 796G.A G266R Missense CCER9 1822G.A G608S Missense Brain CCER10 1390C.A R464X Nonsense CCER11 253-254insC fsP84 Frame shift CCER12 619_627del S207_A209del Deletion AMN-C1 1414-1415insC fsE471 Frame shift AMN-C2 1661G.A R554H Missense AMN-C3 1585delG fsG528 Frame shift Fibroblast AMN-C4 1661G.A R554H Missense AMN-C5 1825G.A E609K Missense AMN-C6 919C.T Q307X Nonsense AMN-C7 1850G.A R617H Missense AMN-C8 887A.G Y296C Missense AMN-C9 965T.C L322P Missense Brain AMN-C10 1390C.T R464X Nonsense AMN-C11 [1165C.T;1224 þ 1GT.TG] [R389C;fSE408] Missense; frame shift AMN-C12 1661G.A R554H Missense AMN-C13 [1997A.C;2007C.G] [Y666S;H669Q] Missense AMN-C14 1755delG fsH586 Frame shift AMN1 529C.T Q177X Nonsense AMN2 1999C.G H667D Missense AMN3 1415delAG fsE471 Frame shift Fibroblast AMN4 337delC fsA112 Frame shift AMN5 310C.T R104C Missense AMN6 919C.T Q307X Nonsense AMN7 323C.T S108L Missense Brain All mutation designations conform to the nomenclature described by Antonarakis and den Dunnen (30,31). Login to comment