|
1091
|
|
|
SS nuclear autoantigen 1 |
N14, NA-14, NA14 |
|
|
1092
|
|
|
Suppressor of cytokine signaling 1 |
AISIMD, CIS1, CISH1, JAB, SOCS-1, SSI-1, SSI1, TIP-3, TIP3 |
|
|
1093
|
|
|
Serpin family A member 6 |
CBG |
|
|
1094
|
|
|
Solute carrier family 4 member 4 |
HNBC1, KNBC, NBC1, NBC2, NBCe1, NBCe1-A, PRTAO, SLC4A5, hhNMC, kNBC1, pNBC |
Asthma, Cataract, Corneal dystrophy, Development disorder, Distal renal tubular acidosis, Glaucoma, Lung adenocarcinoma, Mental retardation, Metabolic acidosis, Proximal renal tubular acidosis, Renal tubular acidosis, Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation |
|
1095
|
|
|
Syntaxin 16 |
SYN-16, SYN16 |
Anxiety disorder, Cataract, Conjunctivitis, Dental enamel hypoplasia, Diaphyseal dysplasia, Dwarfism, Dyskinetic syndrome, Hyperphosphatemia, Hyperpotassemia and hypertension, Hypocalcemic seizures, Hypocalcemic tetany, Isolated somatotropin deficiency, Laryngeal dystonia, Mental depression, Nystagmus, Pseudohypoaldosteronism, Pseudohypoparathyroidism, Somatotropin deficiency, ThyrotoxicosisView all (4 more) |
|
1096
|
|
|
Syntaxin 11 |
FHL4, HLH4, HPLH4 |
|
|
1097
|
|
|
Serpin family H member 1 |
AsTP3, CBP1, CBP2, HSP47, OI10, PIG14, PPROM, RA-A47, SERPINH2, gp46 |
Cerebral infraction, Cerebral thrombosis, Coronary artery disease, Dentinogenesis imperfecta, Dwarfism, Liver cirrhosis, Liver fibrosis, Lung diseases, Macrocephaly, Micrognathism, Micromelia, Nephrolithiasis, Osteogenesis imperfecta, Osteopenia, Respiratory distress syndrome, ScoliosisView all (1 more) |
|
1098
|
|
|
Serpin family B member 7 |
MEGSIN, PPKN, TP55 |
|
|
1099
|
|
|
Sorting nexin 3 |
Grd19, MCOPS8, SDP3 |
|
|
1100
|
|
|
Synaptosome associated protein 23 |
HsT17016, SNAP-23, SNAP23A, SNAP23B |
|
