Gene: [12p13/PXR1] peroxisome receptor 1; peroxin-5; peroxisome biogenesis disorder (MIM:601539), complementation group 2; adrenoleukodystrophy, autosomal neonatal form (MIM:202370); [PEX5 PTS1R ]
REF | CLO,SEQ,STR,MUT "Dodt G &: Nature Genet, 9, 115-125, 1995 LOC "Marynen P &: Genomics, 30, 366-368, 1995 |
SWI | SWISSPROT: P50542 |
KEY | recp |
CLA | coding, basic |
LOC | 12 p13 |
MIM | MIM: 600414 |
SYN | PEX5 PTS1R |
Ссылки:
- Gene: [07q11/ZWS1] Zellweger syndrome 1 (cerebrohepatorenal); [ZS CHR ]
- Gene: [07q2/PEX1] peroxisome biogenesis factor 1; peroxin-1; Refsum disease, infantile form (neonatal adrenoleukodystrophy); Zellweger syndrome; [IRD NALD ZS ]
- Gene: [08q211/PXMP3] peroxisomal membrane protein 3 (35kD, Zellweger syndrome); peroxin-2; peroxisome biogenesis disorder (MIM:601539), complementation group 10; Zellweger syndrome 3; [PEX2 ZWS3 ]
