about
P527
P688
Peroxisome synthesis in the absence of preexisting peroxisomesPEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein importAnalysis of mammalian peroxin interactions using a non-transcription-based bacterial two-hybrid assayA novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees CIsolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disordersPEX5 binds the PTS1 independently of Hsp70 and the peroxin PEX12PEX12 encodes an integral membrane protein of peroxisomes
P921
Q22008726-90BA3FAB-2B51-4518-BCE6-12EEBCF2D1AAQ22010795-46F70DE7-1F15-4354-AC10-534B9B419227Q24300882-BB1AFF4E-39C8-42DF-BE62-E19E35123C9FQ24307402-0AD3973D-34C6-4C0B-8801-EE24A6A13054Q24311606-263559D6-227C-4242-9AF6-32B188ACFE5EQ24322022-B2DCD834-5BBD-41E8-931D-C05E630345FCQ24323122-240C5218-F023-4B39-8D8E-7A8538CDF821
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Peroxisomal biogenesis factor 12
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Peroxisomal biogenesis factor 12
@en
type
label
Peroxisomal biogenesis factor 12
@en
altLabel
PAF-3
@en
PEX12
@en
Peroxin-12
@en
peroxin 12
@en
peroxisome assembly factor 3
@en
peroxisome assembly protein 12
@en
prefLabel
Peroxisomal biogenesis factor 12
@en
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ENSP00000225873
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P7260
3.A.20.1.1