14241
|
|
|
Titin |
CMD1G, CMH9, CMPD4, CMYO5, CMYP5, EOMFC, HMERF, LGMD2J, LGMDR10, MYLK5, SALMY, TMD |
Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Atrial flutter, Centronuclear myopathy, Limb girdle muscular dystrophy, Brugada syndrome, Cardiac arrhythmia, Cardioembolic stroke, Cardiomyopathy, Dilated cardiomyopathy, Cerebral palsy, Progressive contractures limb-girdle weakness muscle dystrophy syndrome, Multiminicore myopathy, Atrioventricular block, Conduction disorder of the heart, Congenital myopathy, Distal muscular dystrophy, Distal myopathy, Early-onset myopathy with fatal cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Long qt syndrome, Restrictive cardiomyopathy, Sick sinus syndrome, Feingold syndrome, Gross motor development delay, Hearing loss, Heart failure, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Limb-girdle muscular dystrophy, Major depressive disorder, Mitral valve prolapse, Muscular dystrophy, Myocarditis, Myopathy, Neuromuscular disease, Orofacial cleft, Polymorphic catecholaminergic ventricular tachycardia, Right ventricular cardiomyopathy, Schizophrenia, Diabetes mellitus type 2, Ventricular fibrillation, Wolff-parkinson-white syndromeView all (30 more) |
14242
|
|
|
Alpha tocopherol transfer protein |
ATTP, AVED, TTP1, alphaTTP |
|
14243
|
|
|
Transthyretin |
ATTR, CTS, CTS1, HEL111, HsT2651, PALB, TBPA, TTN |
Alzheimer disease, Amyloid neuropathy, Amyloid polyneuropathy, Amyloidosis, Brugada syndrome, Cardiomyopathy, Carpal tunnel syndrome, Charcot-marie-tooth disease, Conduction disorder of the heart, Major depressive disorder, Dystransthyretinemic euthyroidal hyperthyroxinemia, Heart disease, Hyperthyroxinemia, Kidney failure, Lung neoplasms, Senile systemic amyloidosis, Transthyretin amyloid cardiomyopathy, Wild-type transthyretin-related amyloidosisView all (3 more) |
14244
|
|
|
Tweety family member 1 |
- |
|
14245
|
|
|
Tweety family member 2 |
C17orf29 |
|
14246
|
|
|
Tweety family member 3 |
- |
|
14247
|
|
|
TUB bipartite transcription factor |
RDOB, rd5 |
|
14248
|
|
|
Tubulin alpha 1a |
B-ALPHA-1, LIS3, TUBA3 |
Basal cell carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Cerebral palsy, Congenital fibrosis of extraocular muscles, Congenital neurologic anomalies, Cryptorchidism, Dandy-walker syndrome, Myoclonic encephalopathy, Fetal akinesia deformation sequence, Global developmental delay, Lissencephaly, Macrogyria, Cortical development malformation, Microcephaly, Movement disorder, Myocardial ischemia, Neurodevelopmental disorder, Pena-shokeir syndrome , Perisylvian syndrome, Tubulinopathy, West syndromeView all (6 more) |
14249
|
|
|
Tubulin alpha 1b |
K-ALPHA-1 |
|
14250
|
|
|
Tubulin alpha 1c |
OZEMA24, TUBA6, bcm948 |
Breast cancer, Cancer, Colorectal cancer, Estrogen-receptor negative breast cancer, Lung cancer, Oocyte maturation defect, Osteoporosis, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma, Stomach neoplasms |
