1001
|
|
|
Transient receptor potential cation channel subfamily V member 6 |
ABP/ZF, CAT1, CATL, ECAC2, HRPTTN, HSA277909, LP6728, ZFAB |
Hereditary chronic pancreatitis, Bladder calculus, Desbuquois syndrome, Hyperparathyroidism, Intestinal hypomagnesemia, Mastocytosis, Nephrolithiasis, Neurotic disorder, Pancreatitis, Polycystic ovary syndrome, Urolithiasis |
1002
|
|
|
Transformation/transcription domain associated protein |
DEDDFA, DFNA75, PAF350/400, PAF400, STAF40, TR-AP, Tra1 |
|
1003
|
|
|
TruB pseudouridine synthase family member 1 |
PUS4 |
|
1004
|
|
|
TruB pseudouridine synthase family member 2 |
CLONE24922 |
|
1005
|
|
|
Testis expressed basic protein 1 |
C6orf10, TSBP |
Asthma, Eczema, Autism, Autoimmune disease, Autoimmune hepatitis, Bipolar disorder, Celiac disease, Lymphocytic leukemia, Obstructive pulmonary disease, Liver cirrhosis, Coronary artery disease, Crohn disease, Graves disease, Hearing loss, Hepatitis c induced liver cirrhosis, Hodgkin lymphoma, Hyperthyroidism, Hypothyroidism, Inflammatory bowel disease, Juvenile idiopathic arthritis, Lung cancer, Membranous glomerulonephritis, Kawasaki disease, Multiple sclerosis, Obesity, Orofacial cleft, Periodontitis, Psoriasis, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Sjogren syndrome, Squamous cell carcinoma, Systemic lupus erythematosus, Diabetes mellitus type 1, Ulcerative colitisView all (21 more) |
1006
|
|
|
TSC complex subunit 1 |
LAM, TSC |
Autism, Brain disease, Hepatocellular carcinoma, Renal cell carcinoma, Squamous cell carcinoma, Cognition disorder, Cortical dysplasia, Cryptogenic west syndrome, Delirium, dementia, and cognitive disorders, Epilepsy, Focal cortical dysplasia, Keratoconus, Intellectual developmental disorder, Mouth neoplasms, Psoriasis, Infantile spasms, Seizures, Tetralogy of fallot, Tuberous sclerosis complex, West syndromeView all (5 more) |
1007
|
|
|
TSC complex subunit 2 |
LAM, PPP1R160, TSC4 |
Autism, Polycystic kidney disease with tuberous sclerosis, Brain disease, Squamous cell carcinoma, Congenital neurologic anomalies, Cryptogenic west syndrome, Cystic fibrosis, Vascular dementia, Epilepsy, Adenomatous polyposis, Focal cortical dysplasia, Intellectual developmental disorder, Kidney neoplasms, Leiomyoma, Myeloid leukemia, Lung neoplasms, Major depressive disorder, Mouth neoplasms, Neurodevelopmental disorder, Obesity, Pancreatic neoplasms, Polycystic kidney disease, Polycystic kidneys, severe infantile with tuberous sclerosis, Infantile spasms, Seizures, Intellectual disability, Tuberous sclerosis complex, West syndrome, XanthinuriaView all (14 more) |
1008
|
|
|
TSC22 domain family member 1 |
HUCEP-2, Ptg-2, TGFB1I4, TSC22 |
|
1009
|
|
|
TSC22 domain family member 2 |
TILZ4a, TILZ4b, TILZ4c |
|
1010
|
|
|
TSC22 domain family member 3 |
DIP, DSIPI, GILZ, TSC-22R |
|
