|
11
|
|
|
X-linked inhibitor of apoptosis |
API3, BIRC4, IAP-3, ILP1, MIHA, XLP2, hIAP-3, hIAP3 |
Acne, Amyotrophic lateral sclerosis, Anemia, Colitis, Encephalitis, Erythema nodosum, Esophagus neoplasm, Fibrinogen deficiency, Folliculitis, Fulminant hepatitis, Hepatic encephalopathy, Hypofibrinogenemia, Immunologic deficiency syndromes, Inflammatory bowel disease, Lateral sclerosis, Lymphocytosis, Lymphohistiocytosis, Lymphoma, Lymphoproliferative disorder, Lymphoproliferative syndrome, x-linked, Ovarian neoplasm, Ovarian cancer, Pancytopenia, SepticemiaView all (9 more) |
|
12
|
|
|
XIAP associated factor 1 |
BIRC4BP, HSXIAPAF1, XIAPAF1 |
|
|
13
|
|
|
Exportin 5 |
exp5 |
|
|
14
|
|
|
X-prolyl aminopeptidase 3 |
APP3, ICP55, NPHPL1 |
|
|
15
|
|
|
Xylosyltransferase 1 |
DBQD2, PXYLT1, XT-I, XT1, XTI, XYLTI, xylT-I |
Acne, Angioid streaks, Camptodactyly of fingers, Clinodactyly, Congenital disorder of glycosylation, Congenital epicanthus, Congenital genu recurvatum, Short clavicles, Congestive heart failure, Desbuquois dysplasia, Desbuquois syndrome, Developmental delay, Diabetes mellitus, Drusen, Duchenne muscular dystrophy, Dwarfism, Dysmorphic features, Epiphyseal dysplasia, Glaucoma, Hypodontia, Hypotrichosis, Leukemia, Macrocephaly, Age-related macular degeneration, Mental retardation, Microcephaly, Mitral valve prolapse, Mitral valve stenosis, Mouth abnormalities, Myopia, Proptosis, Pseudoxanthoma elasticum, Radioulnar synostosis, Renal insufficiency, Restrictive cardiomyopathy, Scoliosis, Stroke, Synophrys, Ventricular septal defectView all (24 more) |
|
16
|
|
|
Xylosyltransferase 2 |
PXYLT2, SOS, XT-II, XT2, xylT-II |
Angioid streaks, Atrial septal defect, Cataract, Congestive heart failure, Drusen, Dysmorphic features, Hearing loss, Age-related macular degeneration, Mental retardation, Microphthalmos, Mitral valve prolapse, Mitral valve stenosis, Mouth abnormalities, Multiple congenital anomalies, Myopia, Neck webbing, Nystagmus, Osteopenia, Osteoporosis, Posteriorly rotated ear, Pseudoxanthoma elasticum, Renal insufficiency, Restrictive cardiomyopathy, Retinal detachment, Scleroderma, Spondyloocular syndrome, Stroke, Ventricular septal defectView all (13 more) |
|
17
|
|
|
X antigen family member 1B |
CT12.1, CT12.1C, CT12.1D, CT12.1E, CT12.1b, CTP9, GAGED2, XAGE-1, XAGE1, XAGE1C, XAGE1D, XAGE1E |
|
|
18
|
|
|
X antigen family member 1A |
CT12.1, CT12.1A, CT12.1B, CTP9, GAGED2, XAGE-1, XAGE1, XAGE1B |
|
|
19
|
|
|
X-box binding protein 1 |
TREB-5, TREB5, XBP-1, XBP2 |
|
|
20
|
|
|
Xanthine dehydrogenase |
XAN1, XO, XOR |
Alopecia, Anaplastic carcinoma, Autism, Cerebral infraction, Breast cancer, Carcinoma, Cerebral thrombosis, Congestive heart failure, Gout, Heart diseases, Heart failure, Hydronephrosis, Hyperuricemia, Involutional depression, Involutional paraphrenia, Mental depression, Myocardial infarction, Myopathy, Psychosis, Pulmonary thromboembolism, Pyelonephritis, XanthinuriaView all (7 more) |
