Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
141 to 150 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

141
Solute carrier family 22 member 12
OAT4L, RST, UAT, URAT1, hURAT1
Gout, Gouty arthritis, Hereditary renal hypouricemia, Hyperuricemia, Kidney failure, Acute kidney insufficiency, Renal hypouricemia, Renal tubular necrosis, Uric acid renal calculus, Uric acid urolithiasis

142
Solute carrier family 26 member 8
AZON, SPGF3, TAT1
Azoospermia, Non-syndromic male infertility due to sperm motility disorder, Schizophrenia, Spermatogenic failure

143
Secretoglobin family 3A member 2
LU103, PNSP1, UGRP1, pnSP-1
Asthma, Breast cancer

144
Solute carrier family 16 member 10
MCT10, PRO0813, TAT1
Psoriatic arthritis

145
Sideroflexin 4
BCRM1, COXPD18, SLC56A4
Combined oxidative phosphorylation deficiency, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Mental retardation

146
Serpin family A member 3
AACT, ACT, GIG24, GIG25
Alpha-1-antichymotrypsin deficiency, Lipoidosis, Prostatic neoplasms, Prostate cancer

147
Short chain dehydrogenase/reductase family 9C member 7
ARCI13, RDHS, SDR-O, SDRO
Congenital ichthyosis, Congenital nonbullous ichthyosiform erythroderma, Dwarfism, Ectropion, Exfoliative dermatitis, Gangrene, Glaucoma, Hyperkeratosis, Hypotrichosis, Ichthyosis, Ichthyosis with hypotrichosis, Impaired cognition, Lamellar ichthyosis, Lung carcinoma, Otitis media
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148
Solute carrier family 15 member 4
FP12591, PHT1, PTR4
Lupus erythematosus, Nonbacterial verrucal endocardiosis

149
Sp7 transcription factor
OI11, OI12, OSX, osterix
Congenital pectus carinatum, Dwarfism, High palate, Micrognathism, Microstomia, Motor delay, Osteogenesis imperfecta, Osteoporosis, Scoliosis

150
Signal peptide peptidase like 3
IMP2, MDHV1887, PRO4332, PSH1, PSL4
Allergic rhinitis, Diabetes mellitus, Eczema, Lupus erythematosus, Mental depression