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

Смотрите также:

  • 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 ]