Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
12231 to 12240 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12231
Solute carrier family 35 member F2
HSNOV1
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Schizophrenia, Squamous cell carcinoma, Vascular dementia

12232
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

12233
Solute carrier family 35 member F4
C14orf36, c14_5373
Attention deficit hyperactivity disorder, Bipolar disorder, Bullous pemphigoid, Major depressive disorder, Schizophrenia

12234
Solute carrier family 35 member F6
ANT2BP, C2orf18, TANGO9
Corneal astigmatism

12235
Solute carrier family 35 member G2
TMEM22
Melanoma, Mitochondrial complex deficiency

12236
Solute carrier family 35 member G3
AMAC1, TMEM21A
Alzheimer disease

12237
Solute carrier family 36 member 1
Dct1, LYAAT1, PAT1, TRAMD3
Autism, Cerebellar ataxia, Glycinuria with/without oxalate urolithiasis, Iminoglycinuria, Oligodendroglioma, Scoliosis, Spinocerebellar ataxia

12238
Solute carrier family 36 member 2
PAT2, TRAMD1
Cannabis abuse, Glycinuria with/without oxalate urolithiasis, Hyperglycinuria, Iminoglycinuria, Oligodendroglioma, Scoliosis, Substance abuse

12239
Solute carrier family 36 member 4
PAT4
Metabolic syndrome, Obesity, Osteoarthritis, Polycystic ovary syndrome, Diabetes mellitus type 2

12240
Solute carrier family 37 member 1
G3PP, SPX1
Obsessive-compulsive disorder