Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11721 to 11730 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11721
SEL1L adaptor subunit of SYVN1 ubiquitin ligase
Hrd3, NEDGSAF, NEDHGFA, PRO1063, SEL1-LIKE, SEL1L1
Neurodevelopmental disorder

11722
SEL1L family member 3
Sel-1L3
Liver cirrhosis, Nonalcoholic fatty liver disease

11723
Selectin E
CD62E, ELAM, ELAM1, ESEL, LECAM2, selectin-e
Atrial fibrillation, Brain ischemia, Cardiovascular disease, Cerebrovascular disorder, Ischemic heart disease, Coronary artery disease, Allergic contact dermatitis, Atopic dermatitis, Hypercholesterolemia, Iga nephropathy, Multiple sclerosis, Myocardial ischemia, Urticaria

11724
Selenium binding protein 1
EHMTO, HEL-S-134P, LPSB, MTO, SBP56, SP56, hSBP
Colorectal neoplasms, Lung neoplasms, Major depressive disorder, Myocardial infarction, Ovarian neoplasms, Psychotic disorders, Schizophrenia, Stomach neoplasms, Diabetes mellitus type 2

11725
Selenoprotein F
Sep-15
Alzheimer disease, Myocardial infarction

11726
Selenoprotein H
C11orf31, C17orf10, SELH
Schizophrenia

11727
Selenoprotein I
EPT1, SELI, SEPI, SPG81
Complex spastic paraplegia, Coronary artery disease, Neurodevelopmental disorder, Spastic paraplegia, Diabetes mellitus type 2

11728
Selenoprotein K
HSPC030, HSPC297, SELK
Dry eye syndrome, Stevens-johnson syndrome, Toxic epidermal necrolysis

11729
Selenoprotein M
SELM, SEPM
Liver cirrhosis

11730
Selenoprotein N
CFTD, CMYO3, CMYP3, MDRS1, RSMD1, RSS, SELN, SEPN1
Multiminicore myopathy, Congenital fiber type disproportion myopathy, Congenital myopathy, Eichsfeld type congenital muscular dystrophy, Muscular dystrophy, Rigid spine muscular dystrophy