Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6414
Gene name Gene Name - the full gene name approved by the HGNC.
Selenoprotein P
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SELENOP
Synonyms (NCBI Gene) Gene synonyms aliases
SELP, SEPP, SEPP1, SeP
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5p12
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a selenoprotein that is predominantly expressed in the liver and secreted into the plasma. This selenoprotein is unique in that it contains multiple selenocysteine (Sec) residues per polypeptide (10 in human), and accounts for most of th
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001887 Process Selenium compound metabolic process IBA 21873635
GO:0002576 Process Platelet degranulation TAS
GO:0005576 Component Extracellular region IBA 21873635
GO:0005576 Component Extracellular region NAS 14718574
GO:0005576 Component Extracellular region TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601484 10751 ENSG00000250722
Protein
UniProt ID P49908
Protein name Selenoprotein P (SeP)
Protein function Might be responsible for some of the extracellular antioxidant defense properties of selenium or might be involved in the transport of selenium. May supply selenium to tissues such as brain and testis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04592 SelP_N 23 248 Selenoprotein P, N terminal region Family
PF04593 SelP_C 251 381 Selenoprotein P, C terminal region Family
Tissue specificity TISSUE SPECIFICITY: Made in the liver and heart and secreted into the plasma. It is also found in the kidney.
Sequence
Sequence length 381
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Platelet degranulation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Carcinoma Carcinoma, Carcinoma, Spindle-Cell, Undifferentiated carcinoma rs121912654, rs555607708, rs786202962, rs1564055259 12376462, 16316942
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
18483336
Colorectal neoplasms Colorectal Neoplasms rs28929483, rs63751108, rs28929484, rs63749831, rs63750047, rs63751207, rs63749811, rs1553350126, rs63750875, rs63750955, rs587776706, rs63750871, rs587776715, rs63751466, rs63750049
View all (1682 more)
18483336
Lung cancer Malignant neoplasm of lung rs121913530, rs121913529, rs878855122, rs1057519784, rs770315135 19058871
Unknown
Disease term Disease name Evidence References Source
Endometriosis Endometriosis 20864642 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Achalasia Addisonianism Alacrimia syndrome Associate 25395084
Adenoma Associate 30469315
Alzheimer Disease Associate 18997300, 20521393, 24914767
Amyotrophic Lateral Sclerosis Associate 23732511
Aneuploidy Associate 22715394
Antithrombin deficiency type 2 Inhibit 39265995
Anxiety Associate 35577822
Aortic Aneurysm Abdominal Associate 25395084, 30188935
Aortic Diseases Associate 25395084, 30188935
Arterial Occlusive Diseases Associate 25395084, 30188935