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"
701 to 710 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

701
Solute carrier family 30 member 5
ZNT5, ZNTL1, ZTL1, ZnT-5
Cardiomyopathy, Dilated cardiomyopathy, Concentric hypertrophic cardiomyopathy, Gout, Hydrops fetalis, Hypertrophic cardiomyopathy

702
Solute carrier family 30 member 6
MST103, MSTP103, ZNT6
Alzheimer disease, Central nervous system cancer, Glioblastoma, Glioma

703
Solute carrier family 30 member 7
ZHS, ZNT7, ZnT-7, ZnTL2
Testis atrophy, Esophageal neoplasms, Aplasia of the vermis, Joubert syndrome, Multiple sclerosis, Neurodevelopmental disorder, Ziegler-huang syndrome

704
Solute carrier family 30 member 8
ZNT8, ZnT-8
Asthma, Breast cancer, Kidney disease, Diabetes mellitus, Diabetes mellitus type 2, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Diffuse idiopathic skeletal hyperostosis, Gestational diabetes, Lung cancer, Metabolic syndrome, Obesity, Psoriasis, Schizophrenia
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705
Solute carrier family 30 member 9
BILAPES, C4orf1, GAC63, HUEL, ZNT9
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Birk-landau-perez syndrome, Major depressive disorder, Neurotic disorder, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

706
Solute carrier family 31 member 1
COPT1, CTR1, NSCT
Congenital abnormalities, Pulmonary hypertension, Intellectual developmental disorder, Liver neoplasms, Necrosis, Prostatic neoplasms

707
Solute carrier family 31 member 2
COPT2, CTR2, hCTR2
Breast cancer

708
Solute carrier family 32 member 1
DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12
Anorexia nervosa, Developmental and epileptic encephalopathy, Generalized epilepsy with febrile seizures plus, Seizure, Intellectual developmental disorder, Obesity, Obsessive-compulsive disorder, Willis-ekbom disease, Schizophrenia

709
Solute carrier family 33 member 1
ACATN, AT-1, AT1, CCHLND, HPBDS, SPG42
Spastic paraplegia, Cataract, Colorectal cancer, Congenital cataract hearing loss developmental delay syndrome, Dementia, Developmental disability, Global developmental delay, Hearing impairment, Hearing loss, Hypothyroidism, Insomnia, Neurotic disorder, Partial epilepsy, Hereditary spastic paraplegia

710
Solute carrier family 34 member 1
FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2
Asthma, Bladder calculus, Bone disease, Kidney and ureter calculus, Kidney disease, Crohn disease, De toni-debre-fanconi syndrome, Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis, Dominant hypophosphatemia with nephrolithiasis or osteoporosis, Fanconi renotubular syndrome, Fanconi syndrome, Hypercalcemia, Idiopathic infantile hypercalcemia, Hypercalciuria, Hypophosphatemic rickets
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