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72129 Pex13

72129

Pex13

peroxisomal biogenesis factor 13

protein-coding

Mus musculus

基因描述

Type Description
Definition peroxisomal biogenesis factor 13

研究结论

Date Results Publications
2020-12-12 13:22:00 Hepatocyte-specific deletion of peroxisomal protein PEX13 results in disrupted iron homeostasis. 32565019
2019-02-02 10:44:00 An increasing reactive gliosis in the PEX13 mutant brain started at E14.5 in association with the pathology 29187321
2011-04-09 10:24:00 PEX13 deficiency leads to mitochondria-mediated oxidative stress, neuronal cell death and impairment of cerebellar development. 20959636
2010-01-21 00:00:00 pex13 has a role in peroxisome biogenesis and its disruption in mice causes a Zellweger syndrome phenotype 12897163
2010-01-21 00:00:00 gene structure, tissue expression, and localization of the protein to peroxisomes 11829486

名称对应

Type IDs
Synonymous 2610008O20Rik
Gene
UniProtKB-ID: PEX13_MOUSE
UniprotKB: Q9D0K1
UniParc: UPI00000218AF
EMBL: AK011355, AK032650, AK029336, AK169148, AK031975, AK031710, AK153438, AF329877, AK029099, AJ304506, BC023683
Ensembl: ENSMUSG00000020283
KO: mmu:72129
Nucleutide sequences
EMBL-CDS: AAH23683.1, AAK15313.2, BAC27971.1, BAE40927.1, BAC27635.1, CAC20705.1, BAC26296.1, BAE31995.1, BAC26402.1, BAB27563.1, BAC27526.1
Ensembl_TRS: ENSMUST00000020523
Protein sequencees
Ensembl_PRO: ENSMUSP00000020523
RefSeq: NP_076140.2
Others
UniRef100: UniRef100_Q9D0K1
UniRef90: UniRef90_Q9D0K1
UniRef50: UniRef50_Q92968
UniGene: Mm.29536, Mm.286622
CCDS: CCDS24478.1

全选

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研究热度

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