|
501
|
|
|
Serrate, RNA effector molecule |
ARS2, ASR2, serrate |
|
|
502
|
|
|
SUFU negative regulator of hedgehog signaling |
BCNS2, JBTS32, PRO1280, SUFUH, SUFUXL |
Accessory rib, Acquired kyphoscoliosis, Acrocallosal syndrome, Agenesis of corpus callosum, Ambiguous genitalia, Amnesia, Arachnodactyly, Asthma, Basal cell neoplasm, Brachycephaly, Brachydactyly, Brain neoplasms, Calcification of falx cerebri, Carcinoma, Cardiac fibroma, Cardiac rhabdomyoma, Cataract, Choanal atresia, Congenital anomaly of neck, Congenital coloboma of iris, Congenital diaphragmatic hernia, Congenital epicanthus, Rib fusion, Congenital hypoplasia of penis, Congenital kyphoscoliosis, Cryptorchidism, Cyclocephaly, Dandy-walker syndrome, Desmoplastic/nodular medulloblastoma, Developmental delay, Duodenal atresia, Dwarfism, Dysarthria, Eczema, Erectile dysfunction, Facial paralysis, Frontal bossing, Fused incisors, Gastrointestinal stromal tumor, Glaucoma, Gorlin syndrome, Growth hormone deficiency, Hearing loss, Hemangioma, Holoprosencephaly, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadotropic hypogonadism, Hypospadias, Hypothalamic hypothyroidism, Hypothyroidism, Inflammatory bowel disease, Mental retardation, Intracranial meningioma, Joubert syndrome, Keratocystic odontogenic tumor, Primitive neuroectodermal tumor, Macrocephaly, Malocclusion, Medulloblastoma, Medulloblastoma with extensive nodularity, Medullomyoblastoma, Melanocytic nevus, Meningioma, Microcephaly, Microform holoprosencephaly, Microphthalmos, Mood swings, Motor delay, Multiple meningioma, Neoplasms, Neurofibroma, Obesity, Oculodentodigital dysplasia, Oculomotor apraxia, Oculomotor nerve palsy, Oculovestibuloauditory syndrome, Orbital cyst, Ovarian cancer, Ovarian carcinoma, Ovarian epithelial carcinoma, Ovarian fibromata, Panhypopituitarism, Papilledema, Polydactyly, Brain stem compression, Proptosis, Renal agenesis, Schizophrenia, Scoliosis, Speech disorders, Spina bifida, Spinal meningioma, Sprengel deformity, Strabismus, Tetralogy of fallot, Tongue neoplasms, Trigeminal neuralgia, Postaxial hand polydactylyView all (84 more) |
|
503
|
|
|
Solute carrier family 26 member 4 |
DFNB4, EVA, PDS, TDH2B |
Compensated hypothyroidism, Congenital sensorineural hearing loss, Deafness, Developmental delay, Dwarfism, Hearing loss, Hyperparathyroidism, Hypersomnia, Hypothyroidism, Mental retardation, Kidney disease, Macroglossia, Mondini defect, Non-syndromic sensorineural deafness, Pendred syndrome, Prostatic neoplasms, Prostate cancer, Sensorineural hearing loss, Speech disorders, Thyroid agenesis, Thyroid carcinoma, Thyroid hypoplasia, Tracheal stenosis, Wolff-parkinson-white syndromeView all (9 more) |
|
504
|
|
|
Serpin family F member 1 |
EPC-1, OI12, OI6, PEDF, PIG35 |
|
|
505
|
|
|
Synaptotagmin 17 |
Syt-17, sytXVII |
|
|
506
|
|
|
Serine/threonine kinase 26 |
MASK, MST4 |
|
|
507
|
|
|
SIX homeobox 4 |
AREC3 |
|
|
508
|
|
|
Solute carrier family 25 member 3 |
OK/SW-cl.48, PHC, PTP, PiC |
|
|
509
|
|
|
Serpin family A member 1 |
A1A, A1AT, AAT, PI, PI1, PRO2275, alpha1AT, nNIF |
Adenocarcinoma, Alpha 1-antitrypsin deficiency, Alveolitis, Anxiety disorder, Arteriosclerosis, Asbestosis, Bipolar disorder, Bronchiectasis, Carcinoma, Cholestasis, Chronic obstructive pulmonary disease, Cystic fibrosis, Degenerative diseases, central nervous system, Digestive system neuroendocrine neoplasm, Emphysema, Fragile x syndrome, Gastric cancer, Hemorrhagic disease, Hypoglycemia, Kidney failure, Liver carcinoma, Liver cirrhosis, Liver failure, Liver fibrosis, Lung neoplasms, Lung cancer, Lung diseases, Manic disorder, Mood disorder, Movement disorders, Nephrotic syndrome, Neurodegenerative disorders, Nodular non-suppurative panniculitis, Panacinar emphysema, Pulmonary emphysema, Pulmonary fibrosis, Reactive hypoglycemia, Acute kidney insufficiency, Stomach neoplasms, Thiamine deficiency, VasculitisView all (26 more) |
|
510
|
|
|
Serpin family A member 4 |
KAL, KLST, KST, PI-4, PI4, kallistatin |
|
