Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
731 to 740 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

731
Solute carrier family 35 member F6
ANT2BP, C2orf18, TANGO9
Corneal astigmatism

732
Solute carrier family 35 member G2
TMEM22
Melanoma, Mitochondrial complex deficiency

733
Solute carrier family 35 member G3
AMAC1, TMEM21A
Alzheimer disease

734
Solute carrier family 36 member 1
Dct1, LYAAT1, PAT1, TRAMD3
Autism, Cerebellar ataxia, Glycinuria with/without oxalate urolithiasis, Iminoglycinuria, Oligodendroglioma, Scoliosis, Spinocerebellar ataxia

735
Solute carrier family 36 member 2
PAT2, TRAMD1
Cannabis abuse, Glycinuria with/without oxalate urolithiasis, Hyperglycinuria, Iminoglycinuria, Oligodendroglioma, Scoliosis, Substance abuse

736
Solute carrier family 36 member 4
PAT4
Metabolic syndrome, Obesity, Osteoarthritis, Polycystic ovary syndrome, Diabetes mellitus type 2

737
Solute carrier family 37 member 1
G3PP, SPX1
Obsessive-compulsive disorder

738
Solute carrier family 37 member 3
SPX3
Androgenetic alopecia, Eye disease, Meniere disease, Enterocolitis, Non-small cell lung carcinoma, Retinitis pigmentosa

739
Solute carrier family 37 member 4
CDG2W, G6PT, G6PT1, G6PT2, G6PT3, GSD1b, GSD1c, GSD1d, PRO0685, SPX4, TRG-19, TRG19
B-cell acute lymphoblastic leukemia, Congenital disorder of glycosylation, Glycogen storage disease, Liver cirrhosis

740
Solute carrier family 38 member 1
ATA1, NAT2, SAT1, SNAT1
Alzheimer disease, Gout, Hypertrophic cardiomyopathy, Multiple sclerosis, Oligodendroglioma, Parkinson disease, Diabetes mellitus type 2