|
391
|
|
|
SAC3 domain containing 1 |
HSU79266, SHD1 |
|
|
392
|
|
|
SEC61 translocon subunit alpha 1 |
ADTKD5, CVID15, HNFJ4, HSEC61, SEC61, SEC61A |
Anemia, Cystic kidney disease, Dwarfism, Glomerulosclerosis, Gout, Hyperuricemia, Hyperuricemic nephropathy, Impaired cognition, Kidney disease, Nephritis, Neutropenia, Renal cyst |
|
393
|
|
|
SERTA domain containing 1 |
SEI1, TRIP-Br1, TRIPBR1 |
|
|
394
|
|
|
Solute carrier family 25 member 24 |
APC1, SCAMC-1, SCAMC1 |
Abnormal dermatoglyphic pattern, Acrocephaly, Aortic aneurysm, Astigmatism, Atrial septal defect, Bicuspid aortic valve, Brachycephaly, Central nervous system neoplasms, Cerebellar hypoplasia, Congenital absent nipple, Congenital craniofacial dysostosis, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Pulmonary hypoplasia, Coronal craniosynostosis, Cryptorchidism, Defect of skull ossification, Dwarfism, Gastroesophageal reflux disease, Glioma, Gorlin chaudhry moss syndrome, Hearing loss, Hydrocephalus, Hyperopia, Hypertrichosis, Hypodontia, Hypoplasia of corpus callosum, Hypoplasia of nipple, Hypoplasia of the maxilla, Left ventricular hypertrophy, Lipoatrophy, Lipodystrophy, Malocclusion, Mental retardation, Microcephaly, Microdontia, Micrognathism, Microphthalmos, Microstomia, Nystagmus, Oligodontia, Patent ductus arteriosus, Penis agenesis, Periventricular nodular heterotopia, Petty laxova wiedemann syndrome, Posteriorly rotated ear, Progeroid syndrome, Proptosis, Pulmonary arterial hypertension, Sclerocornea, Scoliosis, Shagreen patch, Strabismus, Syndactyly, Synophrys, Tricuspid valve insufficiencyView all (42 more) |
|
395
|
|
|
Schwannomin interacting protein 1 |
SCHIP-1 |
|
|
396
|
|
|
Solute carrier family 39 member 3 |
ZIP-3, ZIP3 |
|
|
397
|
|
|
SH3 domain containing kinase binding protein 1 |
AGMX2, CD2BP3, CIN85, GIG10, HSB-1, HSB1, IMD61, MIG18 |
|
|
398
|
|
|
Solute carrier family 40 member 1 |
FPN, FPN1, HFE4, IREG1, MST079, MSTP079, MTP1, SLC11A3 |
Anemia, Apoceruloplasmin deficiency, Arthritis, Autism, Cardiomyopathy, Cataract, Ceruloplasmin deficiency, Cirrhosis, Congenital hepatic fibrosis, Endometrioma, Endometriosis, Erectile dysfunction, Fatty liver, Hemochromatosis, Hereditary hemochromatosis, Intravascular hemolysis, Iron overload, Liver neoplasms, Liver cancerView all (4 more) |
|
399
|
|
|
Serpin family D member 1 |
D22S673, HC2, HCF2, HCII, HLS2, LS2, THPH10 |
|
|
400
|
|
|
SRY-box transcription factor 8 |
- |
|
