Type | Description |
---|---|
Definition | peroxidasin like |
Date | Results | Publications |
---|---|---|
2020-06-20 11:31:00 | We also observe evidence for an excess burden of rare, predicted loss-of-function variation in PXDNL and BMS1- two genes relevant to the broader laterality phenotype. These findings highlight potential new genes in the development of laterality defects, and suggest extensive locus heterogeneity and complex genetic models in this class of birth defects. | 30622330 |
2019-02-23 13:33:00 | the PMR1 pump, a Golgi resident Ca(2+)/Mn(2+) P-type ATPase, plays a pivotal role in regulating the intracellular levels of calcium and manganese ions. | 28780169 |
2017-06-10 11:28:00 | The human PXDN endonuclease stimulates cell motility by down regulating miR-200 family microRNAs. | 27257068 |
2010-12-05 22:08:00 | Observational study of gene-disease association. (HuGE Navigator) | 20800603 |
2010-06-30 22:05:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
Type | IDs |
---|---|
Synonymous | PMR1, PRM1, VPO2 |
Gene |
UniProtKB-ID:
PXDNL_HUMAN
UniprotKB:
A1KZ92
UniParc:
UPI0001AE6ED6,
UPI000049E0C0,
UPI0001EC9666
EMBL:
CH471068,
AK131524,
AC090186,
AC107374,
AY877349,
AC012413,
EU170240,
AK058200,
AC011128,
AC103958
Ensembl:
ENSG00000147485
KO:
hsa:137902
|
Nucleutide sequences |
EMBL-CDS:
ABX24517.1,
BAB71713.1,
BAD18663.1,
EAW86707.1,
AAX70929.1
Ensembl_TRS:
ENST00000356297
|
Protein sequencees |
Ensembl_PRO:
ENSP00000348645
RefSeq:
XP_011515760.1,
NP_653252.4,
XP_005251225.1,
XP_016868530.1
|
Others |
UniRef100:
UniRef100_A1KZ92
UniRef90:
UniRef90_A1KZ92
UniRef50:
UniRef50_A1KZ92
UniGene:
Hs.444882
CCDS:
CCDS47855.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
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