|
471
|
|
|
Solute carrier family 11 member 2 |
AHMIO1, DCT1, DMT1, NRAMP2 |
|
|
472
|
|
|
S-phase cyclin A associated protein in the ER |
IDDRP, MSTP063, ZNF291, Zfp291 |
Attention deficit hyperactivity disorder, Brachydactyly, Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Diverticular diseases, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Intellectual developmental disorder and retinitis pigmentosa, Mental retardation, Keratoconus, Leukemia, Age-related macular degeneration, Nystagmus, Obesity, Obsolete peripheral retinopathy, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophy, Speech disordersView all (7 more) |
|
473
|
|
|
SIX homeobox 6 |
MCOPCT2, ODRMD, OPTX2, Six9 |
Accessory rib, Agenesis of corpus callosum, Anetoderma, Cataract, Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome, Rib fusion, Congenital ocular coloboma, Cryptorchidism, Developmental delay, Dwarfism, Esophageal atresia, Frontal bossing, Glaucoma, Hearing loss, Horizontal nystagmus, Hypogonadotropic hypogonadism, Hypoplasia of corpus callosum, Hypoplasia of spine, Hypoplasia of the optic nerve, Hypospadias, Hypothalamic hamartomas, Isolated microphthalmia, with cataract, Isolated microphthalmia-anophthalmia-coloboma, Spastic diplegia, Microcephaly, Microphthalmia, Syndromic microphthalmia, Microphthalmos, Miosis disorder, Myopia, Nystagmus, Optic disc anomalies with retinal and/or macular dystrophy, Patent ductus arteriosus, Penis agenesis, Retinal dystrophy, Spastic quadriplegia, Specific learning disorder, Ventricular septal defectView all (23 more) |
|
474
|
|
|
SNF2 related chromatin remodeling annealing helicase 1 |
HARP, HHARP |
Anemia, Arteriosclerosis, Astigmatism, Atrioventricular septal defect, Breast cancer, Cafe-au-lait spot, Congenital cataract, Congenital microcephaly, Glomerulosclerosis, Hypertension, Lymphopenia, Malignant neoplasm, Melanocytic nevus, Microdontia, Motor delay, Myopia, Nephrotic syndrome, Neutropenia, Osteopenia, Renal glomerular disease, Renal insufficiency, Schimke immuno-osseous dysplasia, Skeletal dysplasia, Spondyloepiphyseal dysplasia, Spondyloepiphyseal dysplasia nephrotic syndrome, Transient ischemic attackView all (11 more) |
|
475
|
|
|
Synaptonemal complex protein 3 |
COR1, RPRGL4, SCP3, SPGF4 |
|
|
476
|
|
|
Serpin family E member 1 |
PAI, PAI-1, PAI1, PLANH1 |
Atherosclerosis, Autism, Behcet syndrome, Cholestasis, Congenital plasminogen activator inhibitor deficiency, Congestive heart failure, Diabetic nephropathy, Fatty liver, Gastric cancer, Glomerular hyalinosis, Glomerulosclerosis, Heart failure, Hypertension, Kidney failure, Liver neoplasms, Liver cancer, Mental depression, Myocardial infarction, Nephrotic syndrome, Nervous system disorder, Obesity, Plasminogen activator inhibitor-1 deficiency, Prostatic neoplasms, Prostate cancer, Stomach neoplasmsView all (10 more) |
|
477
|
|
|
Serpin family B member 2 |
HsT1201, PAI, PAI-2, PAI2, PLANH2 |
|
|
478
|
|
|
Solute carrier family 45 member 1 |
DNB5, IDDNPF, PAST-A |
Absence of septum pellucidum, Anxiety disorder, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Intellectual developmental disorder with neuropsychiatric features, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Polymicrogyria, Salaam seizures, Schizophrenia, Seizure, Sleep disorders, Stereotyped behaviorView all (7 more) |
|
479
|
|
|
Small nucleolar RNA host gene 32 |
C6orf48, D6S57, G8 |
|
|
480
|
|
|
SH3 and multiple ankyrin repeat domains 1 |
SPANK-1, SSTRIP, synamon |
Anxiety disorder, Autism, Chromophobe carcinoma, Colorectal cancer, Developmental dyspraxia, Motor skills disorders, Nonorganic psychosis, Papillary renal carcinoma, Psychosis, Renal carcinoma, Schizophrenia |
