|
941
|
|
|
Serine/threonine kinase 10 |
LOK, PRO2729 |
|
|
942
|
|
|
Serine/threonine kinase 11 |
LKB1, PJS, hLKB1 |
Adenocarcinoma, Anemia, Ankylosing spondylitis, Azoospermia, Benign neoplasm of testis, Benign tumor of pancreas, Biliary tract neoplasm, Bladder polyp, Breast carcinoma, Carcinoma, Cervical cancer, Cervix carcinoma, Cholangitis, Choriocarcinoma, Colonic neoplasms, Colorectal cancer, Congenital gallbladder anomaly, Crohn disease, Cronkhite-canada syndrome, Cryptorchidism, Endometrial neoplasms, Enlarged polycystic ovaries, Esophagus neoplasm, Gastrointestinal carcinoma, Gonadal dysgenesis, Gynecomastia, Hamartomatous polyposis, Hereditary cancer syndrome, Hypertension, Intestinal neoplasms, Intestinal obstruction, Intestinal polyposis, Intussusception, Iron deficiency anemia, Kidney neoplasm, Left ventricular hypertrophy, Lung adenocarcinoma, Lung cancer, Lung carcinoma, Lung neoplasms, Malignant neoplasm, Malignant neoplasm of testis, Melanoma, Metastatic melanoma, Multiple lentigines, Multiple renal cysts, Nasal polyposis, Neoplasms, Nose cancer, Ovarian cancer, Ovarian carcinoma, Ovarian cysts, Ovarian epithelial carcinoma, Ovarian neoplasm, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic ductal carcinoma, Pancreatic neoplasm, Peutz-jeghers syndrome, Psoriasis, Rectal neoplasms, Rectal prolapse, Renal carcinoma, Stomach carcinoma, Stomach neoplasms, Teratoma, Testicular germ cell tumor, Testicular neoplasms, Ulcerative colitisView all (55 more) |
|
943
|
|
|
Syntaxin 1A |
HPC-1, P35-1, STX1, SYN1A |
|
|
944
|
|
|
Syntaxin 3 |
DIAR12, MVID2, RDMVID, STX3A |
|
|
945
|
|
|
Syntaxin 5 |
CDG2AA, SED5, STX5A |
|
|
946
|
|
|
Syntaxin binding protein 1 |
DEE4, MUNC18-1, N-Sec1, NSEC1, P67, RBSEC1, UNC18, unc-18A, unc18-1 |
9q33.3q34.11 microdeletion syndrome, Attention deficit hyperactivity disorder, Autism, Bilateral convulsive seizures, Camptodactyly of fingers, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Choreoathetosis, Clonic seizures, Congenital exomphalos, Developmental delay, Developmental regression, Dravet syndrome, Dwarfism, Dyscognitive seizures, Dyskinetic syndrome, Dyssomnia, Epilepsy, Epileptic encephalopathy, Episodic ataxia, Febrile seizures, Focal clonic seizures, Focal seizures, Gastroesophageal reflux disease, Hearing loss, Horizontal nystagmus, Hypodontia, Hypoplasia of corpus callosum, Hypotonic seizures, Infantile spasms, Macrostomia, Mental retardation, Microcephaly, Movement disorders, Myoclonic astatic epilepsy, Myoclonic encephalopathy, Myoclonic epilepsy, Myoclonic seizures, Myotonia levior, Nephrolithiasis, Neurodevelopmental disorders, Non-specifi epileptic encephalopathy, Non-syndromic intellectual disability, Nystagmus, Obtundation status, Optic atrophy, Pachygyria, Penis agenesis, Photosensitive tonic-clonic seizures, Precocious puberty, Ptosis, Renal dysplasia, Rett syndrome, Salaam seizures, Schizophrenia, Seizure, Sleep disorders, Spasms syndrome, Spasms x-linked, Spastic paraplegia, Spastic quadriplegia, Status epilepticus, Strabismus, Ureterocele, Ventricular septal defect, West syndromeView all (52 more) |
|
947
|
|
|
Syntaxin binding protein 2 |
FHL5, Hunc18b, MUNC18-2, UNC18-2, UNC18B, pp10122, unc-18B |
|
|
948
|
|
|
Sulfotransferase family 1A member 1 |
HAST1/HAST2, P-PST, P-PST 1, PST, ST1A1, ST1A3, STP, STP1, TSPST1, ts-PST |
Allergic rhinitis, Breast cancer, Mammary neoplasms, Breast carcinoma, Colonic neoplasms, Marfan syndrome, Myocardial ischemia, Prostatic neoplasms, Prostate cancer, Urinary tract cancer, Urologic neoplasms |
|
949
|
|
|
Sulfotransferase family 2B member 1 |
ARCI14, HSST2 |
Cholestasis, Colorectal cancer, Colorectal neoplasms, Congenital nonbullous ichthyosiform erythroderma, Dwarfism, Ectropion, Endometrial neoplasms, Endometrial carcinoma, Exfoliative dermatitis, Gangrene, Hyperkeratosis, Hypotrichosis, Ichthyosis, Ichthyosis congenita, Ichthyosis with hypotrichosis, Impaired cognition, Lamellar ichthyosis, Orthokeratotic hyperkeratosis, Otitis media, Prostatic neoplasms, Prostate cancer, Renal insufficiencyView all (7 more) |
|
950
|
|
|
Sulfite oxidase |
- |
Ankylosing spondylitis, Anxiety disorder, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Celiac disease, Choreoathetosis, Common variable immunodeficiency, Crohn disease, Developmental delay, Diabetes mellitus, Ectopia lentis, Eczema, Isolated sulfite oxidase deficiency, Lupus erythematosus, Psoriasis, Respiratory tract diseases, Rheumatoid arthritis, Spinocerebellar degeneration, Sulfite oxidase deficiency, Sulfocysteinuria, Ulcerative colitisView all (7 more) |
