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
12271 to 12280 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12271
Solute carrier family 6 member 19
B0AT1, HND
Glycinuria with/without oxalate urolithiasis, Hyperglycinuria, Iminoglycinuria, Kidney cancer, Myopia, Uterine fibroid

12272
Solute carrier family 6 member 2
NAT1, NET, NET1, SLC6A5
Bipolar disorder, Cardiac embolism, Cardioembolic stroke, Major depressive disorder, Hyperaldosteronism, Hypertension, Mood disorder, Depression, Schizophrenia, Seizures

12273
Solute carrier family 6 member 20
IMINO, SIT1, XT3, Xtrp3
Glycinuria with/without oxalate urolithiasis, Hirschsprung disease, Hyperglycinuria, Iminoglycinuria, Macular telangiectasia, Mesothelioma, Oligodendroglioma, Osteoarthritis

12274
Solute carrier family 6 member 3
DAT, DAT1, PKDYS, PKDYS1
Amphetamine or sympathomimetic abuse, Anhedonia, Anxiety disorder, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Cerebral amyloid angiopathy, Dopamine transporter deficiency syndrome, Deglutition disorder, Delirium, Dementia, Major depressive disorder, Dyslexia, Genetic predisposition to disease, Hyperkinesia
View all (12 more)

12275
Solute carrier family 6 member 4
5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT, SERT1, hSERT
Amphetamine or sympathomimetic abuse, Anhedonia, Anxiety disorder, Asperger syndrome, Asthma, Attention deficit hyperactivity disorder, Autism, Behavior disorders, Bipolar disorder, Cannabis abuse, Depression, Fatigue syndrome, Obstructive airway disease, Cognition disorder, Congestive heart failure
View all (17 more)

12276
Solute carrier family 6 member 5
GLYT-2, GLYT2, HKPX3, NET1
Apnea, Brain disease, Hereditary hyperekplexia, Hyperekplexia, Hyperexplexia hereditary, Obesity, Psoriasis, Schizophrenia, Diabetes mellitus type 1, Diabetes mellitus type 2

12277
Solute carrier family 6 member 6
HTRDC, TAUT
Bipolar disorder, Myeloid leukemia, Major depressive disorder, Myocardial ischemia, Schizophrenia

12278
Solute carrier family 6 member 7
PROT
Major depressive disorder

12279
Solute carrier family 6 member 8
CCDS1, CRT, CRT-1, CRT1, CRTR, CT1, CTR5
Autism, Cerebral creatine deficiency syndrome, Creatine deficiency, Creatine transporter deficiency, Developmental disability, Intellectual developmental disorder, Internet addiction disorder, Neurodevelopmental disorder, X-linked creatine transporter deficiency, X-linked intellectual disability

12280
Solute carrier family 6 member 9
GCENSG, GLYT1
Amphetamine or sympathomimetic abuse, Attention deficit hyperactivity disorder, Glycine encephalopathy, Autism, Breast cancer, Non-organic psychosis, Psychotic disorders, Schizophrenia, Juvenile idiopathic arthritis