Type | Description |
---|---|
Definition | peroxisomal biogenesis factor 13 |
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 |
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
|
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Refseq |
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