ESAM (gene)

Endothelial cell-selective adhesion molecule is a protein that in humans is encoded by the ESAM gene.^[5][6][7] A mutation in the ESAM gene is known to cause fetal intracranial hemorrhaging.^[8]

ESAM
Identifiers
Aliases	ESAM, W117m, endothelial cell adhesion molecule
External IDs	OMIM: 614281; MGI: 1916774; HomoloGene: 12316; GeneCards: ESAM; OMA:ESAM - orthologs
Gene location (Human) Chr. Chromosome 11 (human)[1] Band 11q24.2 Start 124,752,583 bp[1] End 124,762,290 bp[1]
Gene location (Mouse) Chr. Chromosome 9 (mouse)[2] Band 9|9 A4 Start 37,439,374 bp[2] End 37,449,615 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right lung right lobe of thyroid gland left lobe of thyroid gland upper lobe of left lung right coronary artery popliteal artery tibial arteries apex of heart left coronary artery subcutaneous adipose tissue Top expressed in right lung lobe left lung left lung lobe interventricular septum decidua digastric muscle gastrula cardiac muscles myocardium of ventricle right ventricle More reference expression data BioGPS More reference expression data
Orthologs Species Human Mouse Entrez 90952 69524 Ensembl ENSG00000149564 ENSMUSG00000001946 UniProt Q96AP7 Q925F2 RefSeq (mRNA) NM_138961 NM_027102 RefSeq (protein) NP_620411 NP_081378 Location (UCSC) Chr 11: 124.75 – 124.76 Mb Chr 9: 37.44 – 37.45 Mb PubMed search [3] [4]
Wikidata
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