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Proteintech
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Immunogen sequence: IRAQAAKPC ILFFDEFESI APRRGHDNTG VTDRVVNQLL TQLDGVEGLQ GVYVLAATSR PDLIDPALLR PGRLDKCVYC PPPDQVSRLE ILNVLSDSLP LADDVDLQHV ASVTDSFTGA DLKALLYNAQ LEALHGMLLS SGLQDGSSSS DSDLSLSSMV FLNHSSGSDD SAGDGECGLD QSLVSLEMSE ILPDESKFNM YRLYFGSSYE SELGNGTSSD LSSQCLSAPS SMTQDLPGVP GKDQLFSQPP VLRTASQEGC QELTQEQRDQ LRADISIIKG RYRSQSGEDE SMNQPGPIKT RLAISQSHLM TALGHTRPSI SEDDWKNFAE LYESFQNPKR RKNQSGTMFR PGQKVTLA (927-1283 aa encoded by BC035575)
This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Peroxin-1; Peroxisomal ATPase PEX1; Peroxisome biogenesis disorder protein 1; Peroxisome biogenesis factor 1; Zellweger syndrome
基因别名: 5430414H02Rik; E330005K07Rik; HMLR1; PBD1A; PBD1B; PEX1; RGD1559939; ZWS; ZWS1
UniProt ID: (Human) O43933, (Mouse) Q5BL07
Entrez Gene ID: (Human) 5189, (Rat) 500006, (Mouse) 71382