Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12241 to 12250 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12241
Solute carrier family 37 member 3
SPX3
Androgenetic alopecia, Eye disease, Meniere disease, Enterocolitis, Non-small cell lung carcinoma, Retinitis pigmentosa

12242
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

12243
Solute carrier family 38 member 1
ATA1, NAT2, SAT1, SNAT1
Alzheimer disease, Gout, Hypertrophic cardiomyopathy, Multiple sclerosis, Oligodendroglioma, Parkinson disease, Diabetes mellitus type 2

12244
Solute carrier family 38 member 10
PP1744, SNAT10
Insomnia

12245
Solute carrier family 38 member 11
AVT2
Metabolic syndrome, Open angle glaucoma, Polycystic ovary syndrome, Diabetes mellitus type 2

12246
Solute carrier family 38 member 12
TMEM104
Basal cell carcinoma, Neurodevelopmental disorder

12247
Solute carrier family 38 member 2
ATA2, PRO1068, SAT2, SNAT2
Parkinson disease, Schizophrenia, Diabetes mellitus type 2

12248
Solute carrier family 38 member 3
DEE102, G17, NAT1, SN1, SNAT3
Cannabis abuse, Conotruncal cardiac defect, Major depressive disorder, Developmental and epileptic encephalopathy, Generalized epilepsy, Schizophrenia

12249
Solute carrier family 38 member 5
JM24, SN2, SNAT5, pp7194
Cortical development malformation

12250
Solute carrier family 38 member 6
NAT-1, SNAT6
Color vision deficiency