Type | Description |
---|---|
Definition | protogenin |
Date | Results | Publications |
---|---|---|
2017-12-02 11:16:00 | We found that a burden of low-frequency coding variants in N4BP2, CDSN, PRTG, and AHRR were associated with increased risk of Nonsyndromic cleft lip with or without cleft palate (NSCL/P) . Low-frequency variants in other genes were associated with decreased risk of NSCL/P. These results demonstrate that low-frequency variants contribute to the genetic etiology of NSCL/P | 28425186 |
2014-02-22 12:26:00 | PRTG is regulated by miRNA9, plays an inhibitory action on survival of chondroblasts and articular chondrocytes during chondrogenesis and osteoarthritis pathogenesis. | 24007463 |
2010-01-21 00:00:00 | Identified association of attention deficit hyperactivity disorder (ADHD) to Protogenin (PRTG), a gene that potentially plays a role in cell migration and axon growth. | 19076634 |
2009-01-11 21:30:00 | Observational study of gene-disease association. (HuGE Navigator) | 19076634 |
Type | IDs |
---|---|
Synonymous | IGDCC5 |
Gene |
UniProtKB-ID:
PRTG_HUMAN
UniprotKB:
Q2VWP7
UniParc:
UPI00001555A7
EMBL:
AK098622,
AY630258
Ensembl:
ENSG00000166450
KO:
hsa:283659
|
Nucleutide sequences |
EMBL-CDS:
BAC05355.1,
AAU05741.1
Ensembl_TRS:
ENST00000389286
|
Protein sequencees |
Ensembl_PRO:
ENSP00000373937
RefSeq:
XP_016877571.1,
XP_016877570.1,
XP_011519761.1,
NP_776175.2,
XP_011519762.1
|
Others |
UniRef100:
UniRef100_Q2VWP7
UniRef90:
UniRef90_Q2VWP7
UniRef50:
UniRef50_Q2VWP7
UniGene:
Hs.130957
CCDS:
CCDS42040.1
|
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Refseq |
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