571
|
|
|
SCY1 like pseudokinase 2 |
AMC4, AMCNACC, CVAK104 |
|
572
|
|
|
Septin 11 |
SEPT11, Septin-11 |
|
573
|
|
|
Sodium voltage-gated channel beta subunit 3 |
ATFB16, BRGDA7, HSA243396, SCNB3 |
Atrial fibrillation, Atrioventricular block, Brugada syndrome, Bundle branch block, Cardiac conduction disease, Colorectal cancer, Paroxysmal ventricular tachycardia, Schizoaffective disorder, Sick sinus syndrome, Sinus node dysfunction, Supraventricular tachycardia, Trifascicular block, Ventricular fibrillation |
574
|
|
|
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 |
HSY11339, SIAT7A, ST6GalNAcI, STYI |
|
575
|
|
|
Spermatogenesis associated 7 |
HEL-S-296, HSD-3.1, HSD3, LCA3, RP94 |
Cataract, Ciliopathies, Dysgenesis neuroepithelialis retinae, Congenital cerebral hernia, Congenital hypoplasia of penis, Developmental delay, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hemiplegia/hemiparesis, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosaView all (7 more) |
576
|
|
|
Selenoprotein S |
AD-015, ADO15, SBBI8, SELS, SEPS1, VIMP |
|
577
|
|
|
Solute carrier family 22 member 11 |
OAT4, hOAT4 |
|
578
|
|
|
Sulfatase 2 |
HSULF-2 |
|
579
|
|
|
Solute carrier family 50 member 1 |
HsSWEET1, RAG1AP1, SCP, SWEET1, slv |
|
580
|
|
|
SMG9 nonsense mediated mRNA decay factor |
C19orf61, F17127_1, HBMS, NEDITPO |
Cerebral atrophy, Dandy-walker syndrome, Developmental delay, Gastroesophageal reflux disease, Heart and brain malformation syndrome, Hypoplasia of corpus callosum, Interrupted aortic arch, Microcephaly, Microphthalmos, Posteriorly rotated ear, Ventricular septal defect |