Human Gene SELP (uc001ggi.4)
  Description: Homo sapiens selectin P (granule membrane protein 140kDa, antigen CD62) (SELP), mRNA.
RefSeq Summary (NM_003005): This gene encodes a 140 kDa protein that is stored in the alpha-granules of platelets and Weibel-Palade bodies of endothelial cells. This protein redistributes to the plasma membrane during platelet activation and degranulation and mediates the interaction of activated endothelial cells or platelets with leukocytes. The membrane protein is a calcium-dependent receptor that binds to sialylated forms of Lewis blood group carbohydrate antigens on neutrophils and monocytes. Alternative splice variants may occur but are not well documented. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr1:169,558,088-169,599,377 Size: 41,290 Total Exon Count: 17 Strand: -
Coding Region
   Position: hg19 chr1:169,559,386-169,599,312 Size: 39,927 Coding Exon Count: 16 

Page IndexSequence and LinksUniProtKB CommentsPrimersGenetic AssociationsMalaCards
CTDGene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein Structure
Other SpeciesGO AnnotationsmRNA DescriptionsPathwaysOther NamesModel Information
Methods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr1:169,558,088-169,599,377)mRNA (may differ from genome)Protein (830 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkH-INVHGNCHPRDLynxMalacards
MGIOMIMPubMedTreefamUniProtKBWikipedia
BioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: Q5R349_HUMAN
DESCRIPTION: SubName: Full=P-selectin; SubName: Full=Selectin P (Granule membrane protein 140kDa, antigen CD62); Flags: Fragment;
SIMILARITY: Contains 1 C-type lectin domain.

-  Primer design for this transcript
 

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Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
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To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  Genetic Association Studies of Complex Diseases and Disorders
  Genetic Association Database (archive): SELP
CDC HuGE Published Literature: SELP
Positive Disease Associations: Alzheimer Disease , Atherosclerosis , atherosclerosis, coronary , atopy-susceptibility , Cardiovascular Diseases , cognitive function , Coronary Artery Disease , coronary artery disease; P-selectin , heart disease, ischemic stroke, ischemic , myocardial infarction , nephropathy, IgA , P-selectin , soluble levels of adhesion molecules , thromboembolism, venous
Related Studies:
  1. Alzheimer Disease
    S J Furney et al. Molecular psychiatry 2011, Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease., Molecular psychiatry. [PubMed 21116278]
  2. Atherosclerosis
    Kelly A Volcik , et al. Clinical chemistry 2009 55(6):1076-82, SELP and SELPLG genetic variation is associated with cell surface measures of SELP and SELPLG: the Atherosclerosis Risk in Communities Carotid MRI Study., Clinical chemistry 2009 55(6):1076-82. [PubMed 19395438]
    Specific SELP and SELPLG polymorphisms were associated with cell surface measures of SELP and SELPLG in both whites and African Americans in the ARIC Carotid MRI Study.
  3. atherosclerosis, coronary
    Bugert, P. et al. 2004, Polymorphisms in the P-selectin (CD62P) and P-selectin glycoprotein ligand-1 (PSGL-1) genes and coronary heart disease, Clinical chemistry and laboratory medicine. 2004 ;42(9):997-1004. [PubMed 15497463]
    The molecular characterization of P-selectin and PSGL-1 in a case-control study including CHD patients and healthy controls revealed evidence for association of the genes with development of the disease. However, the functional role of the gene variants should be elucidated by further experimental data.
           more ... click here to view the complete list

-  MalaCards Disease Associations
  MalaCards Gene Search: SELP
Diseases sorted by gene-association score: arteriosclerosis obliterans (28), immune-complex glomerulonephritis (22), intermittent claudication (21), peripheral vascular disease (18), gray platelet syndrome (16), intracranial arteriosclerosis (15), carotid stenosis (15), ehrlichiosis (12), peripheral artery disease (12), mitral valve stenosis (11), cerebrovascular disease (11), von willebrand's disease (10), venous insufficiency (10), thrombocytopenia due to platelet alloimmunization (10), leukocyte adhesion deficiency (10), thrombotic thrombocytopenic purpura (10), acute myocardial infarction (9), blood platelet disease (9), vascular disease (9), retinal vascular occlusion (9), thrombocytosis (8), type 2b von willebrand disease (8), maxillary sinusitis (8), systemic scleroderma (8), essential thrombocythemia (8), heparin-induced thrombocytopenia (8), antiphospholipid syndrome (7), glanzmann thrombasthenia (7), quebec platelet disorder (7), chronic venous insufficiency (7), thrombocytopenic purpura, autoimmune (7), portal vein thrombosis (7), coronary artery disease (7), stroke, ischemic (6), thrombasthenia (6), sickle cell disease (6), generalized atherosclerosis (6), clopidogrel resistance (6), carotid artery thrombosis (5), intermediate coronary syndrome (5), obstructive sleep apnea (5), malaria (5), hermansky-pudlak syndrome 3 (5), common cold (5), primary thrombocytopenia (5), stormorken syndrome (5), multiple symmetrical lipomatosis (5), thrombotic thrombocytopenic purpura, acquired (4), griscelli syndrome, type 1 (4), thrombosis (4), transient global amnesia (4), atrial fibrillation (4), ischemia (3), myocardial infarction (3), arteriosclerosis (3), artery disease (3), asthma (2), autoinflammation, lipodystrophy, and dermatosis syndrome (2), diabetes mellitus, insulin-dependent (2), hypertension, essential (1), diabetes mellitus, noninsulin-dependent (1)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 8.02 RPKM in Lung
Total median expression: 124.94 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -16.9065-0.260 Picture PostScript Text
3' UTR -185.91613-0.303 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR001304 - C-type_lectin
IPR016186 - C-type_lectin-like
IPR018378 - C-type_lectin_CS
IPR016187 - C-type_lectin_fold
IPR016060 - Complement_control_module
IPR000742 - EG-like_dom
IPR013032 - EGF-like_CS
IPR002396 - Selectin_superfamily
IPR000436 - Sushi_SCR_CCP

Pfam Domains:
PF00059 - Lectin C-type domain
PF00084 - Sushi repeat (SCR repeat)

SCOP Domains:
56436 - C-type lectin-like
57535 - Complement control module/SCR domain
57196 - EGF/Laminin

ModBase Predicted Comparative 3D Structure on Q5R349
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The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologGenome BrowserNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGD    
 Protein Sequence    
 Alignment    

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Biological Process:
GO:0007155 cell adhesion

Cellular Component:
GO:0016020 membrane


-  Descriptions from all associated GenBank mRNAs
  LF205427 - JP 2014500723-A/12930: Polycomb-Associated Non-Coding RNAs.
LP895761 - Sequence 625 from Patent EP3253886.
BC028067 - Homo sapiens selectin P (granule membrane protein 140kDa, antigen CD62), mRNA (cDNA clone IMAGE:5212431), partial cds.
BC068533 - Homo sapiens selectin P (granule membrane protein 140kDa, antigen CD62), mRNA (cDNA clone MGC:87370 IMAGE:30349489), complete cds.
M25322 - Human granule membrane protein-140 mRNA, complete cds.
LF320382 - JP 2014500723-A/127885: Polycomb-Associated Non-Coding RNAs.
JD063036 - Sequence 44060 from Patent EP1572962.
LF320381 - JP 2014500723-A/127884: Polycomb-Associated Non-Coding RNAs.
JD088350 - Sequence 69374 from Patent EP1572962.
JD268392 - Sequence 249416 from Patent EP1572962.
JD094471 - Sequence 75495 from Patent EP1572962.
JD246241 - Sequence 227265 from Patent EP1572962.
JD419731 - Sequence 400755 from Patent EP1572962.
JD508701 - Sequence 489725 from Patent EP1572962.
JD172169 - Sequence 153193 from Patent EP1572962.
AK312884 - Homo sapiens cDNA, FLJ93328, highly similar to Homo sapiens selectin P (granule membrane protein 140kDa, antigen CD62) (SELP), mRNA.
AB527801 - Synthetic construct DNA, clone: pF1KB5791, Homo sapiens SELP gene for selectin P, without stop codon, in Flexi system.
KU178327 - Homo sapiens selectin P isoform 1 (SELP) mRNA, partial cds, alternatively spliced.
KU178328 - Homo sapiens selectin P isoform 3 (SELP) mRNA, complete cds, alternatively spliced.
AY367063 - Homo sapiens P-selectin mRNA, partial cds.
JD060899 - Sequence 41923 from Patent EP1572962.
MA441004 - JP 2018138019-A/12930: Polycomb-Associated Non-Coding RNAs.
MA555959 - JP 2018138019-A/127885: Polycomb-Associated Non-Coding RNAs.
MA555958 - JP 2018138019-A/127884: Polycomb-Associated Non-Coding RNAs.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa04514 - Cell adhesion molecules (CAMs)

-  Other Names for This Gene
  Alternate Gene Symbols: NM_003005, NP_002996, Q5R349, Q5R349_HUMAN, RP1-86F14.2-002
UCSC ID: uc001ggi.4
RefSeq Accession: NM_003005
Protein: Q5R349 CCDS: CCDS1282.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_003005.3
exon count: 17CDS single in 3' UTR: no RNA size: 3185
ORF size: 2493CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 5186.00frame shift in genome: no % Coverage: 99.56
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.