ABCD4 p.Gly486Cys
| Predicted by SNAP2: | A: N (87%), C: N (78%), D: N (93%), E: N (87%), F: N (53%), H: N (93%), I: N (82%), K: N (87%), L: N (82%), M: N (78%), N: N (93%), P: N (82%), Q: N (93%), R: N (87%), S: N (97%), T: N (93%), V: N (87%), W: N (61%), Y: N (57%), |
| Predicted by PROVEAN: | A: N, C: N, D: N, E: N, F: N, H: N, I: N, K: N, L: N, M: N, N: N, P: N, Q: N, R: N, S: N, T: N, V: N, W: N, Y: N, |
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[hide] Mutations in ABCD4 cause a new inborn error of vit... Nat Genet. 2012 Oct;44(10):1152-5. doi: 10.1038/ng.2386. Epub 2012 Aug 26. Coelho D, Kim JC, Miousse IR, Fung S, du Moulin M, Buers I, Suormala T, Burda P, Frapolli M, Stucki M, Nurnberg P, Thiele H, Robenek H, Hohne W, Longo N, Pasquali M, Mengel E, Watkins D, Shoubridge EA, Majewski J, Rosenblatt DS, Fowler B, Rutsch F, Baumgartner MR
Mutations in ABCD4 cause a new inborn error of vitamin B(12) metabolism.
Nat Genet. 2012 Oct;44(10):1152-5. doi: 10.1038/ng.2386. Epub 2012 Aug 26., [PMID:22922874]
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Inherited disorders of vitamin B(12) (cobalamin) have provided important clues to how this vitamin, which is essential for hematological and neurological function, is transported and metabolized. We describe a new disease that results in failure to release vitamin B(12) from lysosomes, which mimics the cblF defect caused by LMBRD1 mutations. Using microcell-mediated chromosome transfer and exome sequencing, we identified causal mutations in ABCD4, a gene that codes for an ABC transporter, which was previously thought to have peroxisomal localization and function. Our results show that ABCD4 colocalizes with the lysosomal proteins LAMP1 and LMBD1, the latter of which is deficient in the cblF defect. Furthermore, we show that mutations altering the putative ATPase domain of ABCD4 affect its function, suggesting that the ATPase activity of ABCD4 may be involved in intracellular processing of vitamin B(12).
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No. Sentence Comment
41 Subject 2 carried two mutations that are predicted to disrupt consensus splice sites: c.542+1G>T, located at the 5' splice donor site of intron 5, and c.1456G>T (p.Gly486Cys), located at the last nucleotide of exon 14.
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ABCD4 p.Gly486Cys 22922874:41:164
status: NEW