Peroxisome biogenesis factor 10 is a protein that in humans is encoded by the PEX10 gene. Alternative splicing results in two transcript variants encoding different...
8 KB (975 words) - 21:06, 27 August 2023
commonly, patients have mutations in the PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, or PEX26 genes. In almost all cases...
14 KB (1,378 words) - 09:58, 25 July 2024
retinopathy. PBD-ZSD is most commonly caused by mutations in the PEX1, PEX6, PEX10, PEX12, and PEX26 genes. This results in the over-accumulation of very long...
8 KB (578 words) - 19:15, 22 July 2024
XYYYY syndrome (49,XYYYY) Y 1:1,000,000 males Zellweger syndrome PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX26 recessive...
42 KB (983 words) - 10:34, 21 August 2024
peroxin proteins include: PEX1, PEX2 (PXMP3), PEX3, PEX5, PEX6, PEX7, PEX9, PEX10, PEX11A, PEX11B, PEX11G, PEX12, PEX13, PEX14, PEX16, PEX19, PEX26, PEX28...
33 KB (3,863 words) - 06:13, 27 July 2024
example Peroxisomal biogenesis factor 11. PEX1 PEX2 PEX3 PEX5 PEX6 PEX7 PEX10 PEX11A, PEX11B, PEX11G PEX12 PEX13 PEX14 PEX16 PEX19 PEX26 Crookes WJ, Olsen...
2 KB (133 words) - 18:24, 25 December 2023
may refer to: Neonatal adrenoleukodystrophy Non-alcoholic liver disease PEX10, peroxisome gene PEX13, peroxisome gene This disambiguation page lists articles...
162 bytes (47 words) - 11:51, 22 January 2021
via ubiquitinylation by a membrane complex comprising pex2, pex12, and pex10 followed by an ATP dependent removal involving the cytosolic protein complex...
52 KB (6,402 words) - 02:22, 14 August 2024
NFX1, NFX2, PCGF1, PCGF2, PCGF3, PCGF4, PCGF5, PCGF6, PDZRN3, PDZRN4, PEX10, PHRF1, PJA1, PJA2, PML, PML-RAR, PXMP3, RAD18, RAG1, RAPSN, RBCK1, RBX1...
12 KB (1,259 words) - 10:55, 10 September 2024
HGNC:30024 Q8IYB4 11971 PEX6 HGNC:8859 Q13608 11972 PEX7 HGNC:8860 O00628 11973 PEX10 HGNC:8851 O60683 11974 PEX11A HGNC:8852 O75192 11975 PEX11B HGNC:8853 O96011...
282 KB (17 words) - 07:55, 20 June 2024
PBD complementation groups (CGs). PEX12 has been shown to interact with PEX10, PEX5 and PEX19. GRCh38: Ensembl release 89: ENSG00000108733 – Ensembl,...
9 KB (1,168 words) - 23:34, 29 January 2023
Recessive mitochondrial ataxia syndrome Autosomal recessive ataxia due to PEX10 deficiency Autosomal recessive cerebellar ataxia with late-onset spasticity...
4 KB (426 words) - 16:52, 8 April 2023
; Gärtner, J. (2006). "Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients". Human Mutation. 27 (11):...
10 KB (866 words) - 18:50, 28 August 2023
RER1 gene on the positive strand of chromosome 1.On the minus strand, the PEX10 gene occurs further upstream of Morn1. MORN1 contains 19 different GT-AG...
15 KB (1,434 words) - 06:15, 23 November 2023
DS, Sacksteder KA, Gould SJ (Nov 1999). "PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import"...
12 KB (1,507 words) - 07:44, 4 January 2024
Adrenoleukodystrophy, neonatal; 202370; PEX1 Adrenoleukodystrophy, neonatal; 202370; PEX10 Adrenoleukodystrophy, neonatal; 202370; PEX13 Adrenoleukodystrophy, neonatal;...
234 KB (18,877 words) - 15:43, 9 May 2024
PEX19 gene. PEX19 has been shown to interact with: ABCD1, ABCD2, ABCD3, PEX10, PEX11B, PEX12, PEX13, PEX16, and PEX3. GRCh38: Ensembl release 89: ENSG00000162735...
11 KB (1,270 words) - 13:20, 26 August 2023