Basic Information

SELE

Full name: selectin E

Gene type: protein coding

HGNC ID: HGNC:10718

Gene location: 1q24.2

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/6401

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:10718

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_000450.2

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P16581

AlphaFold: https://alphafold.ebi.ac.uk/entry/P16581

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/131210

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=6401

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa04514+6401

Variant resources

Gene	Disease type	Variant type	NCBI dbSNP	Alleles	Variant location
SELE		3 Prime UTR Variant	rs4786	T>C / T>G	chr1:169722991 (GRCh38.p13)
SELE		Intron Variant	rs3917438	G>A / G>C	chr1:169724709 (GRCh38.p13)
SELE		Missense Variant	rs5368	G>A	chr1:169727805 (GRCh38.p13)
SELE		Intron Variant	rs2076059	C>T	chr1:169729780 (GRCh38.p13)
SELE		Intron Variant	rs3917454	G>A	chr1:169731712 (GRCh38.p13)
SELE		Missense Variant	rs5361	T>A / T>G	chr1:169731919 (GRCh38.p13)