991
|
|
|
Transcriptional repressor GATA binding 1 |
GC79, LGCR |
Alzheimer disease, Androgenetic alopecia, Anorexia nervosa, Attention deficit hyperactivity disorder, Basal cell carcinoma, Bone disease, Brachydactyly, Breast cancer, Congenital anomalies of the kidney and urinary tract, Carcinoma, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Congenital cartilage disorder, Craniofacial abnormalities, Craniosynostosis, Crohn disease, Cutaneous squamous cell carcinoma, Dementia, Desbuquois syndrome, Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Digestive system disease, Diverticular disease, Eating disorder, Endometriosis, Estrogen-receptor negative breast cancer, Gout, Inflammatory bowel disease, Insomnia, Keratinocyte carcinoma, Major depressive disorder, Metabolic syndrome, Metaphyseal chondrodysplasia, Mitral valve prolapse, Neurotic disorder, Non-small cell lung carcinoma, Obesity, Oligodendroglioma, Osteochondrodysplasias, Parkinson disease, Peripheral arterial disease, Schizophrenia, Skin cancer, Skin disease, Skin neoplasms, Squamous cell carcinoma, Trichorhinophalangeal syndrome, Diabetes mellitus type 2, Ulcerative colitis, Uterine polypView all (38 more) |
992
|
|
|
TRNA phosphotransferase 1 |
- |
|
993
|
|
|
Transient receptor potential cation channel subfamily V member 1 |
VR1 |
|
994
|
|
|
Transient receptor potential cation channel subfamily V member 2 |
VRL, VRL-1, VRL1 |
|
995
|
|
|
Transient receptor potential cation channel subfamily V member 3 |
FNEPPK2, OLMS, OLMS1, VRL3 |
|
996
|
|
|
Transient receptor potential cation channel subfamily V member 4 |
BCYM3, CMT2C, HMSN2C, OTRPC4, SMAL, SPSMA, SSQTL1, TRP12, VRL2, VROAC |
Alzheimer disease, Osteonecrosis of the femoral head, Auditory neuropathy, Brachyolmia, Charcot-marie-tooth disease, Congenital benign spinal muscular atrophy, Distal hereditary motor neuropathy, Avascular necrosis of bone, Avascular necrosis of femoral head, Bone disease, Brachyrachia, Obstructive airway disease, Congenital cartilage disorder, Congenital clubfoot, Connective tissue disease, Dejerine-sottas disease, Desbuquois syndrome, Digital arthropathy-brachydactyly, familial, Distal spinal muscular atrophy, Glioma, Gout, Hereditary motor and sensory neuropathies, Motor neuron disease, Hyperalgesia, Hypertrophic neuropathy, Neuromuscular disease, Osteoarthritis, Osteochondrodysplasias, Osteonecrosis of medial femoral condyle, Parastremmatic dwarfism, Peroneal muscle atrophy, Chronic obstructive pulmonary disease, Roussy-levy syndrome, Scapuloperoneal spinal muscular atrophy, Schizophrenia, Skeletal dysplasia, Spinal muscular atrophy, Spondyloepimetaphyseal dysplasia, Spondyloepiphyseal dysplasia, Spondylometaphyseal dysplasia, Urination disordersView all (26 more) |
997
|
|
|
Transient receptor potential cation channel subfamily V member 5 |
CAT2, ECAC1, OTRPC3 |
|
998
|
|
|
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 |
999
|
|
|
Transformation/transcription domain associated protein |
DEDDFA, DFNA75, PAF350/400, PAF400, STAF40, TR-AP, Tra1 |
|
1000
|
|
|
TruB pseudouridine synthase family member 1 |
PUS4 |
|
