SELP (selectin P) - Rat Genome Database

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Gene: SELP (selectin P) Homo sapiens
Analyze
Symbol: SELP
Name: selectin P
RGD ID: 737162
HGNC Page HGNC
Description: Enables several functions, including fucose binding activity; heparin binding activity; and lipopolysaccharide binding activity. Involved in several processes, including calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules; calcium-mediated signaling using intracellular calcium source; and leukocyte tethering or rolling. Located in external side of plasma membrane; extracellular space; and platelet alpha granule membrane. Is integral component of plasma membrane. Implicated in atopic dermatitis and myocardial infarction. Biomarker of several diseases, including Kawasaki disease; autoimmune disease (multiple); coronary artery disease (multiple); obesity; and type 2 diabetes mellitus.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CD62; CD62 antigen-like family member P; CD62P; FLJ45155; GMP-140; GMP140; granule membrane protein 140; granule membrane protein 140kDa; granulocyte membrane protein; GRMP; LECAM3; leukocyte-endothelial cell adhesion molecule 3; P-selectin; PADGEM; platelet activation dependent granule-external membrane protein; platelet alpha-granule membrane protein; PSEL; selectin P (granule membrane protein 140kDa, antigen CD62)
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1169,588,849 - 169,630,193 (-)EnsemblGRCh38hg38GRCh38
GRCh381169,588,849 - 169,630,125 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371169,558,087 - 169,599,362 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361167,824,711 - 167,866,001 (-)NCBINCBI36hg18NCBI36
Build 341166,289,747 - 166,331,065NCBI
Celera1142,667,866 - 142,709,161 (-)NCBI
Cytogenetic Map1q24.2NCBI
HuRef1140,780,771 - 140,822,069 (-)NCBIHuRef
CHM1_11170,980,248 - 171,021,531 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(R)-linalyl acetate  (ISO)
17beta-estradiol  (ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-acetyl-1-alkyl-sn-glycero-3-phosphocholine  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3-[3-(tert-butylsulfanyl)-1-(4-chlorobenzyl)-5-(propan-2-yl)-1H-indol-2-yl]-2,2-dimethylpropanoic acid  (EXP)
3-methylcholanthrene  (ISO)
4-(ethoxymethylene)-2-phenyloxazol-5-one  (ISO)
4-hydroxyphenyl retinamide  (ISO)
6-propyl-2-thiouracil  (ISO)
acetaldehyde  (EXP)
acetamide  (ISO)
acetylsalicylic acid  (EXP)
ADP  (EXP)
aflatoxin B1  (EXP)
aldehydo-D-glucose  (EXP)
all-trans-retinoic acid  (EXP)
amlodipine  (EXP)
ammonium chloride  (ISO)
anandamide  (EXP)
antirheumatic drug  (EXP)
arachidonic acid  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene  (EXP)
biotin  (ISO)
bisphenol A  (ISO)
bivalirudin  (EXP)
budesonide  (ISO)
Calcimycin  (EXP)
cangrelor  (EXP)
carbon monoxide  (EXP)
carbon nanotube  (ISO)
carrageenan  (ISO)
chloramine T  (EXP)
choline  (ISO)
cimetidine  (EXP)
clopidogrel  (ISO)
cobalt dichloride  (ISO)
cocaine  (EXP)
curcumin  (EXP,ISO)
D-glucose  (EXP)
dextran sulfate  (ISO)
diarsenic trioxide  (EXP)
dichlorine  (ISO)
diclofenac  (ISO)
dioxygen  (ISO)
enalapril  (ISO)
endosulfan  (ISO)
estrone  (ISO)
ethanol  (ISO)
fenvalerate  (ISO)
genistein  (ISO)
glucose  (EXP)
heparin  (EXP)
indometacin  (ISO)
L-methionine  (ISO)
lead diacetate  (ISO)
leukotriene C4  (EXP)
leukotriene D4  (EXP)
linalyl acetate  (ISO)
lipopolysaccharide  (ISO)
lipoxin A4  (EXP)
losartan  (ISO)
manganese(II) chloride  (ISO)
methoxychlor  (ISO)
methylmercury chloride  (ISO)
N-acetyl-beta-D-glucosamine  (ISO)
N-acetyl-D-glucosamine  (ISO)
N-formyl-L-methionyl-L-leucyl-L-phenylalanine  (EXP)
nebivolol  (EXP)
nickel atom  (EXP)
nickel sulfate  (ISO)
nitrogen dioxide  (EXP)
obeticholic acid  (ISO)
ozone  (ISO)
paclitaxel  (ISO)
paracetamol  (ISO)
paraquat  (ISO)
parthenolide  (EXP)
PCB138  (ISO)
perfluorooctane-1-sulfonic acid  (EXP)
pioglitazone  (ISO)
pirinixic acid  (ISO)
poly(styrene)  (EXP)
pravastatin  (EXP)
progesterone  (ISO)
quercetin  (EXP,ISO)
resolvin D1  (ISO)
resveratrol  (EXP,ISO)
rosuvastatin calcium  (ISO)
sertraline  (EXP)
silicon dioxide  (ISO)
simvastatin  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP)
sulforaphane  (ISO)
testosterone  (ISO)
tetrachloromethane  (ISO)
theaflavin  (ISO)
titanium dioxide  (EXP,ISO)
tofacitinib  (ISO)
trichostatin A  (EXP)
trimellitic anhydride  (ISO)
U-73122  (EXP)
valproic acid  (EXP)
XL147  (ISO)
zileuton  (EXP,ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
1. Barbaux SC, etal., Arterioscler Thromb Vasc Biol. 2001 Oct;21(10):1668-73.
2. Bourgain C, etal., Am J Hum Genet. 2003 Sep;73(3):612-26. Epub 2003 Aug 15.
3. Carr CL, etal., Arterioscler Thromb Vasc Biol. 2011 Nov;31(11):2526-33.
4. Corsi MM, etal., Biogerontology. 2011 Oct;12(5):451-4. Epub 2011 Apr 12.
5. GOA_HUMAN data from the GO Consortium
6. Hackert T, etal., Pancreatology. 2009;9(4):369-74. Epub 2009 May 19.
7. Hsieh YH, etal., Shock. 2011 Oct;36(4):424-30.
8. Impellizzeri D, etal., Biochem Pharmacol. 2011 Mar 1;81(5):636-48. Epub 2010 Dec 11.
9. Jin AY, etal., BMC Neurosci. 2010 Feb 2;11:12.
10. Kaufmann BA, etal., Arterioscler Thromb Vasc Biol. 2010 Jan;30(1):54-9. Epub 2009 Oct 15.
11. Ling XB, etal., Clin Proteomics. 2010 Dec;6(4):175-193. Epub 2010 Sep 30.
12. Lu HH, etal., Chin Med J (Engl). 2010 Nov;123(21):3123-6.
13. Lu XY, etal., Lupus. 2010 May;19(6):689-95. Epub 2010 Feb 23.
14. Mayne E, etal., J Acquir Immune Defic Syndr. 2011 Dec 9.
15. Musselwhite LW, etal., AIDS. 2011 Mar 27;25(6):787-95.
16. Nagy B Jr, etal., Thromb Haemost. 2007 Jul;98(1):186-91.
17. Oberheiden T, etal., Blood Coagul Fibrinolysis. 2010 Dec;21(8):729-35.
18. OMIM Disease Annotation Pipeline
19. Pan L, etal., Zhonghua Jie He He Hu Xi Za Zhi. 2010 Apr;33(4):265-7.
20. Pipeline to import KEGG annotations from KEGG into RGD
21. Pipeline to import Pathway Interaction Database annotations from NCI into RGD
22. Polanowska-Grabowska R, etal., Arterioscler Thromb Vasc Biol. 2010 Dec;30(12):2392-9. Epub 2010 Nov 11.
23. Polinska B, etal., Folia Histochem Cytobiol. 2011;49(1):119-24.
24. RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
25. RGD automated import pipeline for gene-chemical interactions
26. Ryan J, etal., Lab Invest. 2011 Dec;91(12):1727-38. doi: 10.1038/labinvest.2011.137. Epub 2011 Sep 5.
27. Schafer A, etal., Eur J Heart Fail. 2009 Apr;11(4):336-41. Epub 2009 Feb 3.
28. Schneider DJ, etal., Diabetes Care. 2009 May;32(5):944-9. Epub 2009 Feb 19.
29. Schreiber O, etal., Am J Physiol Gastrointest Liver Physiol. 2009 Mar;296(3):G534-42. Epub 2009 Jan 15.
30. Sellam J, etal., Arthritis Res Ther. 2009;11(5):R156. Epub 2009 Oct 15.
31. Senchenkov E, etal., Microcirculation. 2011 Aug;18(6):452-62. doi: 10.1111/j.1549-8719.2011.00106.x.
32. Straface E, etal., Biochem Biophys Res Commun. 2010 Feb 12;392(3):426-30. Epub 2010 Jan 15.
33. Sun XP, etal., Zhong Xi Yi Jie He Xue Bao. 2008 May;6(5):524-9.
34. Tregouet DA, etal., Hum Mol Genet. 2002 Aug 15;11(17):2015-23.
35. Vachharajani V, etal., Microcirculation. 2010 Aug;17(6):407-16.
36. Vaduganathan M, etal., Am Heart J. 2008 Nov;156(5):1002.e1-1002.e7.
37. Varughese GI, etal., J Intern Med. 2007 Apr;261(4):384-91.
38. Wong CK, etal., J Clin Immunol. 2008 Jan;28(1):36-43. Epub 2007 Nov 17.
39. Xue F, etal., Anat Rec (Hoboken). 2008 Aug;291(8):1016-22.
40. Xue M, etal., Mol Med Report. 2011 Jul-Aug;4(4):693-6. doi: 10.3892/mmr.2011.485. Epub 2011 May 5.
41. Yang W, etal., Life Sci. 2011 Feb 14;88(7-8):302-6. Epub 2010 Dec 10.
42. Zhao S, etal., Dig Dis Sci. 2009 Apr 1.
43. Zhong M, etal., Antimicrob Agents Chemother. 2012 Mar 5.
44. Zhou BR, etal., Chin Med J (Engl). 2011 Nov;124(22):3768-72.
45. Zhou Z, etal., Arterioscler Thromb Vasc Biol 2002 Oct 1;22(10):1598-603.
Additional References at PubMed
PMID:1375831   PMID:1377048   PMID:1435334   PMID:1694218   PMID:1701178   PMID:1705568   PMID:1717161   PMID:2466574   PMID:2472431   PMID:7505680   PMID:7508745   PMID:7680663  
PMID:7684381   PMID:7693674   PMID:8467233   PMID:8901515   PMID:9128259   PMID:9129046   PMID:9290466   PMID:9668170   PMID:10391209   PMID:10499919   PMID:10713099   PMID:10733515  
PMID:10950950   PMID:11040019   PMID:11081633   PMID:11237770   PMID:11247301   PMID:11861803   PMID:11885026   PMID:11936588   PMID:11981814   PMID:12036879   PMID:12036880   PMID:12082590  
PMID:12200386   PMID:12384485   PMID:12468916   PMID:12477932   PMID:12736150   PMID:12757775   PMID:12783114   PMID:12847232   PMID:12858167   PMID:12860908   PMID:12871503   PMID:12871600  
PMID:12888879   PMID:12911583   PMID:12945872   PMID:14557872   PMID:14568956   PMID:14592723   PMID:14615387   PMID:14630802   PMID:14676308   PMID:14680834   PMID:14681304   PMID:14764537  
PMID:15026421   PMID:15059608   PMID:15059609   PMID:15080580   PMID:15133030   PMID:15217824   PMID:15221968   PMID:15231569   PMID:15297306   PMID:15297307   PMID:15299021   PMID:15316595  
PMID:15351857   PMID:15353601   PMID:15497463   PMID:15543334   PMID:15583743   PMID:15633604   PMID:15705928   PMID:15769472   PMID:15879141   PMID:15885758   PMID:15916851   PMID:15972662  
PMID:16014051   PMID:16100264   PMID:16125711   PMID:16139336   PMID:16184405   PMID:16257118   PMID:16263699   PMID:16332977   PMID:16344560   PMID:16352650   PMID:16390014   PMID:16514062  
PMID:16633357   PMID:16636497   PMID:16648968   PMID:16683915   PMID:16764881   PMID:16860607   PMID:16877367   PMID:16928730   PMID:16935700   PMID:16973503   PMID:16982492   PMID:17027652  
PMID:17064811   PMID:17074110   PMID:17126824   PMID:17143564   PMID:17192395   PMID:17204688   PMID:17275499   PMID:17279322   PMID:17393020   PMID:17420019   PMID:17437524   PMID:17473568  
PMID:17488661   PMID:17497038   PMID:17498578   PMID:17509958   PMID:17510305   PMID:17554801   PMID:17597069   PMID:17632516   PMID:17634906   PMID:17698171   PMID:17700216   PMID:17702963  
PMID:17706337   PMID:17710630   PMID:17849054   PMID:17890399   PMID:17939599   PMID:17944986   PMID:17945332   PMID:17982310   PMID:18029348   PMID:18034324   PMID:18050247   PMID:18054198  
PMID:18080800   PMID:18182036   PMID:18191640   PMID:18217430   PMID:18333373   PMID:18363812   PMID:18363816   PMID:18383329   PMID:18390200   PMID:18449419   PMID:18497306   PMID:18535285  
PMID:18539899   PMID:18550060   PMID:18576930   PMID:18580442   PMID:18597952   PMID:18600034   PMID:18606703   PMID:18649055   PMID:18713749   PMID:18818407   PMID:18828734   PMID:18974840  
PMID:18974842   PMID:19028820   PMID:19036374   PMID:19047793   PMID:19064610   PMID:19074885   PMID:19082691   PMID:19105599   PMID:19106004   PMID:19118202   PMID:19131662   PMID:19132251  
PMID:19136145   PMID:19138666   PMID:19212907   PMID:19221099   PMID:19240957   PMID:19241310   PMID:19247692   PMID:19262138   PMID:19263529   PMID:19264679   PMID:19280705   PMID:19332769  
PMID:19361981   PMID:19395438   PMID:19404301   PMID:19423540   PMID:19452728   PMID:19479237   PMID:19493436   PMID:19525192   PMID:19536175   PMID:19559392   PMID:19578796   PMID:19590054  
PMID:19638712   PMID:19656773   PMID:19689998   PMID:19729601   PMID:19812370   PMID:19874461   PMID:19913121   PMID:19913879   PMID:19948214   PMID:19948975   PMID:20010946   PMID:20034466  
PMID:20051472   PMID:20056442   PMID:20079524   PMID:20097880   PMID:20153702   PMID:20167578   PMID:20205626   PMID:20227257   PMID:20376705   PMID:20406964   PMID:20431845   PMID:20431848  
PMID:20435690   PMID:20438785   PMID:20445017   PMID:20452482   PMID:20485444   PMID:20536507   PMID:20580062   PMID:20586826   PMID:20602615   PMID:20603037   PMID:20628086   PMID:20669347  
PMID:20673868   PMID:20723301   PMID:20855565   PMID:21085001   PMID:21106229   PMID:21116278   PMID:21143192   PMID:21149548   PMID:21159528   PMID:21170343   PMID:21245745   PMID:21319374  
PMID:21385561   PMID:21441381   PMID:21497813   PMID:21507293   PMID:21521525   PMID:21534853   PMID:21544708   PMID:21545688   PMID:21594636   PMID:21618132   PMID:21638248   PMID:21642543  
PMID:21658254   PMID:21714704   PMID:21763287   PMID:21803846   PMID:21816455   PMID:21866298   PMID:21873635   PMID:22010135   PMID:22021370   PMID:22039451   PMID:22053609   PMID:22068558  
PMID:22088599   PMID:22100896   PMID:22142906   PMID:22159147   PMID:22192915   PMID:22425972   PMID:22472781   PMID:22473907   PMID:22593709   PMID:22627390   PMID:22688557   PMID:22703881  
PMID:22717029   PMID:22745009   PMID:22836626   PMID:22842622   PMID:22862794   PMID:23014585   PMID:23018521   PMID:23382219   PMID:23416763   PMID:23421771   PMID:23442851   PMID:23468382  
PMID:23525448   PMID:23593361   PMID:23740526   PMID:24192766   PMID:24244398   PMID:24271554   PMID:24415745   PMID:24435325   PMID:24498435   PMID:24516598   PMID:24534074   PMID:24589269  
PMID:24601701   PMID:24684681   PMID:24699516   PMID:24940335   PMID:24980694   PMID:25000467   PMID:25057500   PMID:25089002   PMID:25095634   PMID:25108430   PMID:25147926   PMID:25197418  
PMID:25238546   PMID:25297946   PMID:25384966   PMID:25390649   PMID:25405250   PMID:25425738   PMID:25428141   PMID:25498912   PMID:25601896   PMID:25633343   PMID:25682040   PMID:25714598  
PMID:25722429   PMID:25744700   PMID:25747934   PMID:25794792   PMID:25869560   PMID:25948279   PMID:26045295   PMID:26051909   PMID:26068309   PMID:26125797   PMID:26261613   PMID:26261626  
PMID:26279254   PMID:26344728   PMID:26388436   PMID:26418972   PMID:26439305   PMID:26539491   PMID:26575878   PMID:26613867   PMID:26627825   PMID:26631722   PMID:26871637   PMID:26962963  
PMID:27101095   PMID:27102967   PMID:27234491   PMID:27237221   PMID:27267514   PMID:27406211   PMID:27423570   PMID:27775438   PMID:27975100   PMID:28011641   PMID:28097631   PMID:28155729  
PMID:28262902   PMID:28318371   PMID:28358707   PMID:28625976   PMID:28646244   PMID:28770875   PMID:28819827   PMID:29077161   PMID:29203267   PMID:29334682   PMID:29378361   PMID:29517629  
PMID:29739756   PMID:29922946   PMID:30047017   PMID:30068374   PMID:30093507   PMID:30171023   PMID:30340092   PMID:30617759   PMID:30784176   PMID:30795966   PMID:31113254   PMID:31160622  
PMID:31169028   PMID:31212795   PMID:31260799   PMID:31371443   PMID:31520401   PMID:31852401   PMID:31897593   PMID:32000410   PMID:32053880   PMID:32110917   PMID:32429899   PMID:32831023  
PMID:33232787   PMID:33805059   PMID:34015287  


Genomics

Comparative Map Data
SELP
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1169,588,849 - 169,630,193 (-)EnsemblGRCh38hg38GRCh38
GRCh381169,588,849 - 169,630,125 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371169,558,087 - 169,599,362 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361167,824,711 - 167,866,001 (-)NCBINCBI36hg18NCBI36
Build 341166,289,747 - 166,331,065NCBI
Celera1142,667,866 - 142,709,161 (-)NCBI
Cytogenetic Map1q24.2NCBI
HuRef1140,780,771 - 140,822,069 (-)NCBIHuRef
CHM1_11170,980,248 - 171,021,531 (-)NCBICHM1_1
Selp
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391163,942,833 - 163,977,595 (+)NCBIGRCm39mm39
GRCm39 Ensembl1163,942,833 - 163,977,595 (+)Ensembl
GRCm381164,115,264 - 164,150,026 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1164,115,264 - 164,150,026 (+)EnsemblGRCm38mm10GRCm38
MGSCv371166,045,509 - 166,079,876 (+)NCBIGRCm37mm9NCBIm37
MGSCv361165,952,053 - 165,986,420 (+)NCBImm8
MGSCv361165,306,067 - 165,340,774 (+)NCBImm8
Celera1166,568,384 - 166,587,846 (+)NCBICelera
Cytogenetic Map1H2.2NCBI
cM Map171.42NCBI
Selp
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21376,476,229 - 76,511,846 (+)NCBImRatBN7.2
Rnor_6.0 Ensembl1382,429,063 - 82,464,628 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01382,428,914 - 82,464,629 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01387,308,435 - 87,344,164 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41379,886,614 - 79,922,180 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11379,910,278 - 79,936,368 (+)NCBI
Celera1376,209,805 - 76,244,685 (+)NCBICelera
RH 3.4 Map13482.6RGD
Cytogenetic Map13q23NCBI
Selp
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554627,652,437 - 7,693,994 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554627,658,371 - 7,692,870 (+)NCBIChiLan1.0ChiLan1.0
SELP
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11148,793,677 - 148,834,701 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1148,793,677 - 148,834,701 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01145,071,094 - 145,112,851 (-)NCBIMhudiblu_PPA_v0panPan3
SELP
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1728,956,428 - 28,997,266 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl728,958,486 - 28,996,313 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha728,490,155 - 28,527,988 (+)NCBI
ROS_Cfam_1.0728,758,392 - 28,799,283 (+)NCBI
UMICH_Zoey_3.1728,608,516 - 28,646,330 (+)NCBI
UNSW_CanFamBas_1.0728,644,251 - 28,682,064 (+)NCBI
UU_Cfam_GSD_1.0728,881,019 - 28,918,852 (+)NCBI
LOC101970607
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934499,229,898 - 99,265,758 (+)NCBI
SpeTri2.0NW_00493648117,076,660 - 17,112,501 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SELP
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl481,365,740 - 81,406,203 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1481,376,804 - 81,401,240 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2489,001,468 - 89,025,903 (+)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103230618
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12559,420,910 - 59,465,140 (+)NCBI
ChlSab1.1 Ensembl2559,433,333 - 59,462,598 (+)Ensembl
Vero_WHO_p1.0NW_02366605561,082,227 - 61,140,767 (+)NCBI
Selp
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248267,510,039 - 7,544,332 (-)NCBI

Position Markers
AL033775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371169,571,381 - 169,571,488UniSTSGRCh37
Build 361167,838,005 - 167,838,112RGDNCBI36
Celera1142,681,160 - 142,681,267RGD
Cytogenetic Map1q22-q25UniSTS
HuRef1140,794,065 - 140,794,172UniSTS
SHGC-17253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371169,558,142 - 169,558,272UniSTSGRCh37
Build 361167,824,766 - 167,824,896RGDNCBI36
Celera1142,667,921 - 142,668,051RGD
Cytogenetic Map1q22-q25UniSTS
HuRef1140,780,826 - 140,780,956UniSTS
Stanford-G3 RH Map16514.0UniSTS
NCBI RH Map11497.8UniSTS
GeneMap99-G3 RH Map16470.0UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2199
Count of miRNA genes:530
Interacting mature miRNAs:569
Transcripts:ENST00000263686, ENST00000367786, ENST00000367788, ENST00000367791, ENST00000367792, ENST00000367793, ENST00000367794, ENST00000367795, ENST00000426706, ENST00000458599, ENST00000466167
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 496 817 274 22 268 10 1293 245 466 72 427 788 13 940 774 1
Low 1811 2145 1325 488 1186 338 2547 1663 537 285 884 603 152 1 264 1778 3 2
Below cutoff 25 26 93 89 256 90 259 238 2184 22 51 27 2 236

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245439 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245440 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF542391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH001473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL022146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY367063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC028067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC068533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA926598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA994564 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L01574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M25322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z99572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000263686   ⟹   ENSP00000263686
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1169,588,849 - 169,630,124 (-)Ensembl
RefSeq Acc Id: ENST00000367786   ⟹   ENSP00000356760
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1169,589,514 - 169,630,076 (-)Ensembl
RefSeq Acc Id: ENST00000367788   ⟹   ENSP00000356762
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1169,590,147 - 169,630,193 (-)Ensembl
RefSeq Acc Id: ENST00000367795   ⟹   ENSP00000356769
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1169,603,026 - 169,630,086 (-)Ensembl
RefSeq Acc Id: ENST00000426706   ⟹   ENSP00000391694
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1169,588,849 - 169,619,219 (-)Ensembl
RefSeq Acc Id: ENST00000458599   ⟹   ENSP00000399368
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1169,590,147 - 169,630,077 (-)Ensembl
RefSeq Acc Id: ENST00000466167
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1169,589,077 - 169,591,570 (-)Ensembl
RefSeq Acc Id: NM_003005   ⟹   NP_002996
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381169,588,849 - 169,630,124 (-)NCBI
GRCh371169,558,087 - 169,599,377 (-)ENTREZGENE
Build 361167,824,711 - 167,866,001 (-)NCBI Archive
HuRef1140,780,771 - 140,822,069 (-)ENTREZGENE
CHM1_11170,980,248 - 171,021,531 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005245435   ⟹   XP_005245492
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381169,588,849 - 169,630,125 (-)NCBI
GRCh371169,558,087 - 169,599,377 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005245436   ⟹   XP_005245493
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381169,589,572 - 169,630,125 (-)NCBI
GRCh371169,558,087 - 169,599,377 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005245438   ⟹   XP_005245495
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381169,588,849 - 169,630,125 (-)NCBI
GRCh371169,558,087 - 169,599,377 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005245439   ⟹   XP_005245496
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381169,588,849 - 169,630,125 (-)NCBI
GRCh371169,558,087 - 169,599,377 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005245440   ⟹   XP_005245497
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381169,588,849 - 169,630,125 (-)NCBI
GRCh371169,558,087 - 169,599,377 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_002996   ⟸   NM_003005
- Peptide Label: precursor
- UniProtKB: P16109 (UniProtKB/Swiss-Prot),   A0A024R8Y9 (UniProtKB/TrEMBL),   Q6NUL9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245497   ⟸   XM_005245440
- Peptide Label: isoform X3
- UniProtKB: Q5R341 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245496   ⟸   XM_005245439
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_005245495   ⟸   XM_005245438
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_005245492   ⟸   XM_005245435
- Peptide Label: isoform X1
- UniProtKB: P16109 (UniProtKB/Swiss-Prot),   A0A024R8Y9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245493   ⟸   XM_005245436
- Peptide Label: isoform X1
- UniProtKB: P16109 (UniProtKB/Swiss-Prot),   A0A024R8Y9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000391694   ⟸   ENST00000426706
RefSeq Acc Id: ENSP00000399368   ⟸   ENST00000458599
RefSeq Acc Id: ENSP00000356760   ⟸   ENST00000367786
RefSeq Acc Id: ENSP00000356762   ⟸   ENST00000367788
RefSeq Acc Id: ENSP00000356769   ⟸   ENST00000367795
RefSeq Acc Id: ENSP00000263686   ⟸   ENST00000263686
Protein Domains
C-type lectin   EGF-like   Sushi

Promoters
RGD ID:6858072
Promoter ID:EPDNEW_H2201
Type:initiation region
Name:SELP_1
Description:selectin P
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381169,630,121 - 169,630,181EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_003005.4(SELP):c.2266A>C (p.Thr756Pro) single nucleotide variant SELECTIN P POLYMORPHISM [RCV000014482] Chr1:169594713 [GRCh38]
Chr1:169563951 [GRCh37]
Chr1:1q24.2
benign
NM_003005.4(SELP):c.1918G>C (p.Val640Leu) single nucleotide variant SELECTIN P POLYMORPHISM [RCV000014483] Chr1:169596108 [GRCh38]
Chr1:169565346 [GRCh37]
Chr1:1q24.2
risk factor|benign
GRCh38/hg38 1q23.1-25.1(chr1:157747246-176021247)x3 copy number gain See cases [RCV000051854] Chr1:157747246..176021247 [GRCh38]
Chr1:157717036..175990383 [GRCh37]
Chr1:155983660..174257006 [NCBI36]
Chr1:1q23.1-25.1
pathogenic
GRCh38/hg38 1q23.3-25.2(chr1:164922655-180061589)x3 copy number gain See cases [RCV000051856] Chr1:164922655..180061589 [GRCh38]
Chr1:164891892..180030724 [GRCh37]
Chr1:163158516..178297347 [NCBI36]
Chr1:1q23.3-25.2
pathogenic
GRCh38/hg38 1q24.2-25.1(chr1:168314822-175299299)x1 copy number loss See cases [RCV000053918] Chr1:168314822..175299299 [GRCh38]
Chr1:168284060..175268435 [GRCh37]
Chr1:166550684..173535058 [NCBI36]
Chr1:1q24.2-25.1
pathogenic
GRCh38/hg38 1q24.2(chr1:169623984-169744043)x1 copy number loss See cases [RCV000053919] Chr1:169623984..169744043 [GRCh38]
Chr1:169593222..169713184 [GRCh37]
Chr1:167859846..167979808 [NCBI36]
Chr1:1q24.2
pathogenic
GRCh38/hg38 1q23.3-25.1(chr1:161740907-173965154)x1 copy number loss See cases [RCV000053914] Chr1:161740907..173965154 [GRCh38]
Chr1:161710697..173934292 [GRCh37]
Chr1:159977321..172200915 [NCBI36]
Chr1:1q23.3-25.1
pathogenic
GRCh38/hg38 1q23.3-24.3(chr1:164036599-171252077)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053916]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053916]|See cases [RCV000053916] Chr1:164036599..171252077 [GRCh38]
Chr1:164005836..171221216 [GRCh37]
Chr1:162272460..169487840 [NCBI36]
Chr1:1q23.3-24.3
pathogenic
GRCh38/hg38 1q24.1-25.1(chr1:166762832-175327423)x1 copy number loss See cases [RCV000053917] Chr1:166762832..175327423 [GRCh38]
Chr1:166732069..175296559 [GRCh37]
Chr1:164998693..173563182 [NCBI36]
Chr1:1q24.1-25.1
pathogenic
NM_003005.3(SELP):c.2249A>G (p.Glu750Gly) single nucleotide variant Malignant melanoma [RCV000059983] Chr1:169594730 [GRCh38]
Chr1:169563968 [GRCh37]
Chr1:167830592 [NCBI36]
Chr1:1q24.2
not provided
NM_003005.3(SELP):c.1666C>T (p.Arg556Ter) single nucleotide variant Malignant melanoma [RCV000059984] Chr1:169603065 [GRCh38]
Chr1:169572303 [GRCh37]
Chr1:167838927 [NCBI36]
Chr1:1q24.2
not provided
GRCh38/hg38 1q24.2-25.2(chr1:169218236-178075834)x1 copy number loss See cases [RCV000137128] Chr1:169218236..178075834 [GRCh38]
Chr1:169187474..178044969 [GRCh37]
Chr1:167454098..176311592 [NCBI36]
Chr1:1q24.2-25.2
pathogenic
GRCh38/hg38 1q23.3-25.1(chr1:163382523-175877022)x1 copy number loss See cases [RCV000143292] Chr1:163382523..175877022 [GRCh38]
Chr1:163352313..175846158 [GRCh37]
Chr1:161618937..174112781 [NCBI36]
Chr1:1q23.3-25.1
pathogenic
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2
pathogenic
NM_003005.4(SELP):c.775+1G>A single nucleotide variant Premature coronary artery disease [RCV000157648] Chr1:169612928 [GRCh38]
Chr1:169582166 [GRCh37]
Chr1:1q24.2
likely pathogenic
GRCh37/hg19 1q24.2-25.3(chr1:169423492-180367623) copy number gain not provided [RCV000767621] Chr1:169423492..180367623 [GRCh37]
Chr1:1q24.2-25.3
pathogenic
NM_003005.4(SELP):c.1195T>C (p.Cys399Arg) single nucleotide variant not provided [RCV000768086] Chr1:169609642 [GRCh38]
Chr1:169578880 [GRCh37]
Chr1:1q24.2
uncertain significance
NM_003005.4(SELP):c.1366G>T (p.Glu456Ter) single nucleotide variant not provided [RCV000768085] Chr1:169607102 [GRCh38]
Chr1:169576340 [GRCh37]
Chr1:1q24.2
uncertain significance
NM_003005.4(SELP):c.985G>A (p.Ala329Thr) single nucleotide variant not provided [RCV000768087] Chr1:169611654 [GRCh38]
Chr1:169580892 [GRCh37]
Chr1:1q24.2
uncertain significance
Single allele deletion 1q24q25 microdeletion syndrome [RCV000754969] Chr1:169095250..175778910 [GRCh37]
Chr1:1q24.2-25.1
pathogenic
GRCh37/hg19 1q23.3-25.3(chr1:161676893-184071723)x1 copy number loss See cases [RCV000447098] Chr1:161676893..184071723 [GRCh37]
Chr1:1q23.3-25.3
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q23.2-25.1(chr1:160369890-175796325) copy number loss not provided [RCV000767779] Chr1:160369890..175796325 [GRCh37]
Chr1:1q23.2-25.1
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q23.2-25.2(chr1:159815642-177026983)x1 copy number loss not provided [RCV000736717] Chr1:159815642..177026983 [GRCh37]
Chr1:1q23.2-25.2
pathogenic
GRCh37/hg19 1q24.2(chr1:169578789-169580892)x1 copy number loss not provided [RCV000749233] Chr1:169578789..169580892 [GRCh37]
Chr1:1q24.2
benign
NM_003005.4(SELP):c.2018A>G (p.Asn673Ser) single nucleotide variant not provided [RCV000963782] Chr1:169596008 [GRCh38]
Chr1:169565246 [GRCh37]
Chr1:1q24.2
benign
NM_003005.4(SELP):c.2019C>T (p.Asn673=) single nucleotide variant not provided [RCV000914734] Chr1:169596007 [GRCh38]
Chr1:169565245 [GRCh37]
Chr1:1q24.2
likely benign
NM_003005.4(SELP):c.2352T>G (p.Gly784=) single nucleotide variant not provided [RCV000933099] Chr1:169593660 [GRCh38]
Chr1:169562898 [GRCh37]
Chr1:1q24.2
likely benign
NM_003005.4(SELP):c.1855T>G (p.Ser619Ala) single nucleotide variant not provided [RCV000958512] Chr1:169597027 [GRCh38]
Chr1:169566265 [GRCh37]
Chr1:1q24.2
benign
NM_003005.4(SELP):c.384C>T (p.Asn128=) single nucleotide variant not provided [RCV000963419] Chr1:169617125 [GRCh38]
Chr1:169586363 [GRCh37]
Chr1:1q24.2
benign
GRCh37/hg19 1q24.2(chr1:169148346-169806006)x1 copy number loss not provided [RCV001005151] Chr1:169148346..169806006 [GRCh37]
Chr1:1q24.2
uncertain significance
NM_003005.4(SELP):c.821C>T (p.Thr274Ile) single nucleotide variant not provided [RCV000961321] Chr1:169612357 [GRCh38]
Chr1:169581595 [GRCh37]
Chr1:1q24.2
benign
NM_003005.4(SELP):c.2301T>C (p.Thr767=) single nucleotide variant not provided [RCV000955810] Chr1:169593711 [GRCh38]
Chr1:169562949 [GRCh37]
Chr1:1q24.2
benign
NM_003005.4(SELP):c.1334-3T>C single nucleotide variant not provided [RCV000955811] Chr1:169607137 [GRCh38]
Chr1:169576375 [GRCh37]
Chr1:1q24.2
benign
GRCh37/hg19 1q24.2-25.1(chr1:167430471-174635618)x1 copy number loss not provided [RCV001005149] Chr1:167430471..174635618 [GRCh37]
Chr1:1q24.2-25.1
pathogenic
GRCh37/hg19 1q24.2(chr1:169499658-169558108)x1 copy number loss not provided [RCV001258482] Chr1:169499658..169558108 [GRCh37]
Chr1:1q24.2
uncertain significance
NM_003005.4(SELP):c.479C>T (p.Thr160Ile) single nucleotide variant not provided [RCV001280979] Chr1:169617030 [GRCh38]
Chr1:169586268 [GRCh37]
Chr1:1q24.2
uncertain significance
NM_003005.4(SELP):c.1499C>T (p.Ser500Phe) single nucleotide variant not provided [RCV001280981] Chr1:169606969 [GRCh38]
Chr1:169576207 [GRCh37]
Chr1:1q24.2
uncertain significance
NM_003005.4(SELP):c.1879C>A (p.Pro627Thr) single nucleotide variant not provided [RCV001280982] Chr1:169597003 [GRCh38]
Chr1:169566241 [GRCh37]
Chr1:1q24.2
uncertain significance
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:10721 AgrOrtholog
COSMIC SELP COSMIC
Ensembl Genes ENSG00000174175 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000263686 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000356760 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000356762 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000356769 UniProtKB/TrEMBL
  ENSP00000391694 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000399368 UniProtKB/TrEMBL
Ensembl Transcript ENST00000263686 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000367786 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000367788 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000367795 UniProtKB/TrEMBL
  ENST00000426706 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000458599 UniProtKB/TrEMBL
Gene3D-CATH 3.10.100.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000174175 GTEx
HGNC ID HGNC:10721 ENTREZGENE
Human Proteome Map SELP Human Proteome Map
InterPro C-type_lectin-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  C-type_lectin-like/link_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  C-type_lectin_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CTDL_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Selectin_CTLD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Selectin_superfamily UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sushi/SCR/CCP_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sushi_SCR_CCP_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6403 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 6403 ENTREZGENE
OMIM 173610 OMIM
Pfam EGF UniProtKB/TrEMBL
  Lectin_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sushi UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA35643 PharmGKB
PRINTS SELECTIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE C_TYPE_LECTIN_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  C_TYPE_LECTIN_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SUSHI UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART CCP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CLECT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56436 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57535 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R8Y9 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z4F5_HUMAN UniProtKB/TrEMBL
  A0A0S2Z509_HUMAN UniProtKB/TrEMBL
  F6VVT6_HUMAN UniProtKB/TrEMBL
  LYAM3_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q5R341 ENTREZGENE, UniProtKB/TrEMBL
  Q5R342_HUMAN UniProtKB/TrEMBL
  Q5R345_HUMAN UniProtKB/TrEMBL
  Q5R349_HUMAN UniProtKB/TrEMBL
  Q6NUL9 ENTREZGENE, UniProtKB/TrEMBL
  Q8N1E9_HUMAN UniProtKB/TrEMBL
UniProt Secondary Q5R344 UniProtKB/Swiss-Prot
  Q5R348 UniProtKB/TrEMBL
  Q8IVD1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 SELP  selectin P    selectin P (granule membrane protein 140kDa, antigen CD62)  Symbol and/or name change 5135510 APPROVED
2011-08-16 SELP  selectin P (granule membrane protein 140kDa, antigen CD62)  SELP  selectin P (granule membrane protein 140kDa, antigen CD62)  Symbol and/or name change 5135510 APPROVED