|
1021
|
|
|
Signal peptide, CUB domain and EGF like domain containing 1 |
- |
|
|
1022
|
|
|
SPHK1 interactor, AKAP domain containing |
SKIP |
|
|
1023
|
|
|
Sp6 transcription factor |
AI1K, EPFN, EPIPROFIN, KLF14 |
|
|
1024
|
|
|
SHOC2 leucine rich repeat scaffold protein |
NSLH1, SIAA0862, SOC2, SUR8 |
Atrial septal defect, Brachydactyly, Cardiofaciocutaneous syndrome, Facial dysmorphism, Congenital epicanthus, Congenital pectus excavatum, Costello syndrome, Cryptorchidism, Dwarfism, Dysmorphic features, Hair diseases, Hydrocephalus, Hypertrophic cardiomyopathy, Leopard syndrome, Macrocephaly, Macrotia, Mental retardation, Multiple congenital anomalies, Neck webbing, Noonan syndrome, Noonan-like syndrome with loose anagen hair, Posteriorly rotated ear, Pulmonary stenosis, Strabismus, Turner syndrome, male, Ventricular septal defectView all (11 more) |
|
1025
|
|
|
Solute carrier family 19 member 3 |
BBGD, THMD2, THTR2, hTHTR2, thTr-2 |
Anemia, Basal ganglia diseases, Cerebellar ataxia, Craniofacial dystonia, Developmental delay, Dysarthria, Dysphagia, Epileptic encephalopathy, External ophthalmoplegia, Extrapyramidal disease, Hypertrichosis, Hypertrophic cardiomyopathy, Mental retardation, Leigh syndrome, Leigh syndrome with leukodystrophy, Lenticulostriate disorders, Leukodystrophy, Mood swings, Necrotizing encephalomyelopathy, Nervous system diseases, Nystagmus, Optic atrophy, Ptosis, Retinitis pigmentosa, Spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome, Spastic quadriplegia, Status epilepticus, Strabismus, Ventricular septal defect, West syndromeView all (15 more) |
|
1026
|
|
|
Solute carrier family 35 member G2 |
TMEM22 |
|
|
1027
|
|
|
Solute carrier family 44 member 4 |
C6orf29, CTL4, DFNA72, NG22, TPPT, hTPPT1 |
Colorectal cancer, Deafness, Diabetes mellitus, Exudative macular degeneration, Hearing loss, Lung carcinoma, Lupus erythematosus, Multiple sclerosis, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Rheumatoid arthritis, Sarcoidosis, Ulcerative colitis, Vitiligo |
|
1028
|
|
|
Sarcospan |
DAGA5, KRAG, NSPN, SPN1, SPN2 |
|
|
1029
|
|
|
SET domain containing 7, histone lysine methyltransferase |
KMT7, SET7, SET7/9, SET9 |
|
|
1030
|
|
|
Solute carrier family 2 member 10 |
ATORS, ATS, GLUT10 |
Aortic dissection, Aortic valve insufficiency, Aortic valve sclerosis, Arachnodactyly, Arterial tortuosity syndrome, Asthma, Avascular necrosis of the capital femoral epiphysis, Blepharophimosis, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Cardiomyopathy, Congenital diaphragmatic hernia, Congenital exomphalos, Congenital keratoglobus, Congenital pectus carinatum, Congenital pectus excavatum, Congestive heart failure, Craniosynostosis, Cutis laxa, Developmental delay, Eosinophilia, Gastroesophageal reflux disease, Hernia, femoral, Hiatal hernia, High palate, Hypertension, Hypertrophic cardiomyopathy, Ischemic stroke, Keratoconus, Legg-calve-perthes disease, Macrocephaly, Macrotia, Marfan syndrome, Mental retardation, Micrognathism, Moyamoya disease, Myocardial infarction, Myocarditis, Myopia, Respiratory failure, Scoliosis, Specific learning disorder, Strabismus, Thoracic aortic aneurysm and aortic dissection, Ventricular hypertrophy, Vertical talusView all (33 more) |
