Type | Description |
---|---|
Definition | selectin P |
Date | Results | Publications |
---|---|---|
2021-03-20 13:27:00 | Putative functional non-coding polymorphisms in SELP significantly modulate sP-selectin levels, arterial stiffness and type 2 diabetes mellitus susceptibility. | 32429899 |
2021-03-13 13:16:00 | The Ser290Asn and Thr715Pro Polymorphisms of the SELP Gene Are Associated with A Lower Risk of Developing Acute Coronary Syndrome and Low Soluble P-Selectin Levels in A Mexican Population (double dagger). | 32053880 |
2021-01-16 15:55:00 | P-selectin (CD62P) and soluble TREM-like transcript-1 (sTLT-1) are associated with coronary artery disease: a case control study. | 32831023 |
2020-12-05 12:57:00 | Glycosaminoglycans as Tools to Decipher the Platelet Tumor Cell Interaction: A Focus on P-Selectin. | 32110917 |
2020-11-21 13:24:00 | Effect of the expression of CD62P and thrombin generation on patients using central venous catheters for hemodialysis. | 31520401 |
Type | IDs |
---|---|
Synonymous | CD62, CD62P, GMP140, GRMP, LECAM3, PADGEM, PSEL |
Gene |
UniProtKB-ID:
LYAM3_HUMAN,
A0A024R8Y9_HUMAN,
Q6NUL9_HUMAN,
Q5R341_HUMAN
UniprotKB:
P16109,
A0A024R8Y9,
Q6NUL9,
Q5R341
UniParc:
UPI000183CB79,
UPI0000204D4A,
UPI00004708C7,
UPI0000352C26
EMBL:
M60233,
M60234,
M60227,
CH471067,
M60224,
M25322,
M60219,
M60218,
M60226,
M60232,
M60222,
M60225,
AL022146,
M60229,
BC068533,
M60231,
M60217,
KF455060,
AF542391,
Z99572,
M60223,
M60228
Ensembl:
ENSG00000174175
KO:
hsa:6403
|
Nucleutide sequences |
EMBL-CDS:
AAA35910.1,
AAA35911.1,
EAW90851.1,
AAN06828.1,
EAW90853.1,
AAH68533.1,
EAW90850.1
Gene_ORFName:
hCG_38007,
hCG_38007
Ensembl_TRS:
ENST00000263686,
ENST00000367786
|
Protein sequencees |
Ensembl_PRO:
ENSP00000263686,
ENSP00000356760
RefSeq:
XP_005245492.1,
XP_005245497.1,
XP_005245493.1,
XP_005245496.1,
XP_005245495.1,
NP_002996.2
|
Others |
UniRef100:
UniRef100_A0A024R8Y9,
UniRef100_Q5R341,
UniRef100_P16109,
UniRef100_Q6NUL9
UniRef90:
UniRef90_G1RYC2,
UniRef90_P16109
UniRef50:
UniRef50_P16109,
UniRef50_G1RYC2
UniGene:
Hs.73800
CCDS:
CCDS1282.1
|
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Refseq |
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