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"
821 to 830 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

821
Solute carrier family 6 member 19
B0AT1, HND
Glycinuria with/without oxalate urolithiasis, Hyperglycinuria, Iminoglycinuria, Kidney cancer, Myopia, Uterine fibroid

822
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

823
Solute carrier family 6 member 20
IMINO, SIT1, XT3, Xtrp3
Glycinuria with/without oxalate urolithiasis, Hirschsprung disease, Hyperglycinuria, Iminoglycinuria, Macular telangiectasia, Mesothelioma, Oligodendroglioma, Osteoarthritis

824
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)

825
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)

826
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

827
Solute carrier family 6 member 6
HTRDC, TAUT
Bipolar disorder, Myeloid leukemia, Major depressive disorder, Myocardial ischemia, Schizophrenia

828
Solute carrier family 6 member 7
PROT
Major depressive disorder

829
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

830
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