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3621
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Sirtuin 1 |
SIR2, SIR2L1, SIR2alpha |
Atherosclerosis, Atrial fibrillation, Autoimmune diseases, Bipolar disorder, Brain neoplasms, Brain infarction, Breast cancer, Mammary neoplasms, Breast carcinoma, Intracranial neoplasm, Cirrhosis, Colitis, Congestive heart failure, Degenerative diseases, central nervous system, Demyelinating diseases, Diabetes mellitus, Diabetic retinopathy, Fatty liver, Heart diseases, Heart failure, Kidney failure, Marfan syndrome, Metabolic syndrome, Mood disorder, Myocardial infarction, Neurodegenerative disorders, Neuronal ceroid lipofuscinosis, Non-alcoholic fatty liver disease, Obesity, Osteosarcoma, Paroxysmal atrial fibrillation, Prostatic neoplasms, Prostate cancer, Acute kidney insufficiency, Retinal diseases, Schizophrenia, SclerodermaView all (22 more) |
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3622
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Neuronal calcium sensor 1 |
FLUP, FREQ |
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3623
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Zinc finger protein, FOG family member 2 |
DIH3, FOG2, SRXY9, ZC2HC11B, ZNF89B, hFOG-2 |
46, xy partial gonadal dysgenesis, 46, xy sex reversal, Ambiguous genitalia, Asthma, Attention deficit hyperactivity disorder, Azoospermia, Bipolar disorder, Brachydactyly, Breast carcinoma, Camptodactyly of fingers, Cardiovascular diseases, Chronic obstructive pulmonary disease, Congenital diaphragmatic hernia, Pulmonary hypoplasia, Congenital malrotation of intestine, Conotruncal heart defect, Coronary artery disease, Cryptorchidism, Development disorder, Dolichocephaly, Double outlet right ventricle, Glaucoma, Gonadal dysgenesis, Gynecomastia, Hypertrophy of clitoris, Hypogonadism, Hypoplasia of vagina, Hypospadias, Low tension glaucoma, Mental depression, Nephroblastoma, Nephrotic syndrome, Osteoporosis, Ovarian gonadoblastoma, Penis agenesis, Physiologic amenorrhea, Proptosis, Schizophrenia, Streak ovary, Testicular gonadoblastoma, Testicular regression syndrome, Tetralogy of fallotView all (27 more) |
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3624
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Potassium voltage-gated channel subfamily H member 4 |
BEC2, ELK1, Kv12.3 |
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3625
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Malonyl-CoA decarboxylase |
MCD |
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3626
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Crumbs cell polarity complex component 1 |
CRB1-A, CRB1-B, CRB1-C, LCA8, RP12 |
Ankylosing spondylitis, Arthritis, Asthma, Autoimmune diseases, Autoimmune thyroiditis, Bestrophinopathy, Cataract, Celiac disease, Ciliopathies, Common variable immunodeficiency, Dysgenesis neuroepithelialis retinae, Congenital cerebral hernia, Congenital hypoplasia of penis, Crohn disease, Developmental delay, Diabetes mellitus, Disorder of eye, Esotropia, Exudative retinopathy, Glaucoma, Hearing loss, Hemiplegia/hemiparesis, Hyperinsulinism, Hyperopia, Hypogonadism, Keratoconus, Leber congenital amaurosis, Lupus erythematosus, Macular dystrophy, Malformation of cortical development, Mental depression, Mental retardation, Microphthalmos, Nanophthalmos, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Oral ulcer, Paravenous chorioretinal atrophy, Pendular nystagmus, Pigmented paravenous chorioretinal atrophy, Polycystic ovary syndrome, Psoriasis, Retinal detachment, Retinal dystrophy, Retinal pigment epithelial detachment, Retinitis pigmentosa, Rod-cone dystrophy, Stargardt disease, Ulcerative colitis, Vitreoretinal degenerationView all (37 more) |
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3627
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Integrin subunit beta 3 binding protein |
CENP-R, CENPR, HSU37139, NRIF3, TAP20 |
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3628
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|
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Tudor domain containing 7 |
CATC4, PCTAIRE2BP, TRAP |
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3629
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|
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Glutamate receptor interacting protein 1 |
FRASRS3, GRIP |
Abnormal spinal segmentation, Ambiguous genitalia, Amyotrophic lateral sclerosis, Atresia of vagina, Bipolar disorder, Congenital atresia of trachea, Congenital cerebral hernia, Congenital exomphalos, Pulmonary hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Cryptophthalmos, Cryptorchidism, Disorder of eye, Ectopic anus, Female pseudohermaphroditism, Fraser syndrome, Hearing loss, High palate, Hydrops fetalis, Hypospadias, Imperforate anus, Kidney disease, Lacrimal duct aplasia, Laryngostenosis, Meningomyelocele, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microtia, Multicystic renal dysplasia, Polydactyly, Renal hypoplasia, Syndactyly of fingers, Syndactyly of the toes, Syndromic microphthalmia, Tracheal stenosis, Urethral atresiaView all (25 more) |
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3630
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Solute carrier family 7 member 8 |
LAT2, LPI-PC1 |
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