ABCD3 p.Asn148Ser

Predicted by SNAP2: A: N (66%), C: N (66%), D: N (78%), E: N (57%), F: D (71%), G: N (82%), H: N (78%), I: D (63%), K: N (57%), L: D (66%), M: D (66%), P: D (59%), Q: N (87%), R: N (57%), S: N (93%), T: N (87%), V: D (66%), W: D (75%), Y: N (57%),
Predicted by PROVEAN: A: D, C: D, D: N, E: D, F: D, G: N, H: D, I: D, K: D, L: D, M: D, P: D, Q: D, R: D, S: N, T: D, V: D, W: D, Y: D,

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[hide] Takano H, Koike R, Onodera O, Sasaki R, Tsuji S
Mutational analysis and genotype-phenotype correlation of 29 unrelated Japanese patients with X-linked adrenoleukodystrophy.
Arch Neurol. 1999 Mar;56(3):295-300., [PMID:10190819] [PubMed]

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[hide] Unterrainer G, Molzer B, Forss-Petter S, Berger J
Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy.
Hum Mol Genet. 2000 Nov 1;9(18):2609-16., [PMID:11063720] [PubMed]

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[hide] Smith KD, Kemp S, Braiterman LT, Lu JF, Wei HM, Geraghty M, Stetten G, Bergin JS, Pevsner J, Watkins PA
X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.
Neurochem Res. 1999 Apr;24(4):521-35., [PMID:10227685] [PubMed]

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