biogenesis factor 3 is a protein that in humans is encoded by the PEX3 gene. PEX3 has been shown to interact with PEX19. GRCh38: Ensembl release 89:...
9 KB (1,117 words) - 04:31, 27 August 2023
insertion of peroxisomal membrane proteins (PMPs) requires the peroxins PEX19, PEX3, and PEX16. PEX19 is a PMP receptor and chaperone, which binds the PMPs and...
33 KB (3,863 words) - 06:13, 27 July 2024
of peroxisomes. Most commonly, patients have mutations in the PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, or PEX26 genes. In...
14 KB (1,378 words) - 09:58, 25 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...
43 KB (983 words) - 04:37, 11 August 2024
Name OMIM Gene ICD-10 Zellweger syndrome 214100 PEX1, PEX2, PEX3, PEX5, PEX6, PEX12, PEX14, PEX26 Q87.82 Infantile Refsum disease 266510 PEX1, PEX2, PEX26...
8 KB (578 words) - 19:15, 22 July 2024
transmembrane proteins, for example Peroxisomal biogenesis factor 11. PEX1 PEX2 PEX3 PEX5 PEX6 PEX7 PEX10 PEX11A, PEX11B, PEX11G PEX12 PEX13 PEX14 PEX16 PEX19...
2 KB (133 words) - 18:24, 25 December 2023
HGNC:40045 Q6UWS5 11966 PEX1 HGNC:8850 O43933 11967 PEX2 HGNC:9717 P28328 11968 PEX3 HGNC:8858 P56589 11969 PEX5 HGNC:9719 P50542 11970 PEX5L HGNC:30024 Q8IYB4...
282 KB (17 words) - 07:55, 20 June 2024
interact with: ABCD1, ABCD2, ABCD3, PEX10, PEX11B, PEX12, PEX13, PEX16, and PEX3. GRCh38: Ensembl release 89: ENSG00000162735 – Ensembl, May 2017 GRCm38:...
11 KB (1,270 words) - 13:20, 26 August 2023
peroxisome assembly. Most commonly, patients have mutations in the PEX1, PEX3, PEX6, PEX12, and PEX26 genes. In almost all cases, patients have mutations...
10 KB (866 words) - 18:50, 28 August 2023
syndrome; 214100; PXF Zellweger syndrome, complementation group G; 214100; PEX3 Zellweger syndrome-1; 214100; PEX1 https://www.ncbi.nlm.nih.gov/Omim/omimfaq...
234 KB (18,877 words) - 15:43, 9 May 2024