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"
721 to 730 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

721
Solute carrier family 35 member E4
-
Atrial fibrillation

722
Solute carrier family 35 member F1
C6orf169, dJ230I3.1
Aortic valve disease, Atrial fibrillation, Attention deficit hyperactivity disorder, Bipolar disorder, Bladder exstrophy, Coronary artery disease, Heart failure, Hypertension, Hypertrophic cardiomyopathy, Malunion fracture, Metabolic syndrome, Nephrotic syndrome, Neurodevelopmental disorder, Oligodendroglioma, Psychiatric disorders
View all (2 more)

723
Solute carrier family 35 member F2
HSNOV1
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Schizophrenia, Squamous cell carcinoma, Vascular dementia

724
Solute carrier family 35 member F3
-
Alzheimer disease, Brain aneurysm, Brain infarction, Obstructive pulmonary disease, Colorectal cancer, Dementia, Digestive system disease, Diverticular disease, Diverticulitis, Hypertension, Insomnia, Obstructive sleep apnea syndrome, Scoliosis

725
Solute carrier family 35 member F4
C14orf36, c14_5373
Attention deficit hyperactivity disorder, Bipolar disorder, Bullous pemphigoid, Major depressive disorder, Schizophrenia

726
Solute carrier family 35 member F6
ANT2BP, C2orf18, TANGO9
Corneal astigmatism

727
Solute carrier family 35 member G2
TMEM22
Melanoma, Mitochondrial complex deficiency

728
Solute carrier family 35 member G3
AMAC1, TMEM21A
Alzheimer disease

729
Solute carrier family 36 member 1
Dct1, LYAAT1, PAT1, TRAMD3
Autism, Cerebellar ataxia, Glycinuria with/without oxalate urolithiasis, Iminoglycinuria, Oligodendroglioma, Scoliosis, Spinocerebellar ataxia

730
Solute carrier family 36 member 2
PAT2, TRAMD1
Cannabis abuse, Glycinuria with/without oxalate urolithiasis, Hyperglycinuria, Iminoglycinuria, Oligodendroglioma, Scoliosis, Substance abuse