190861
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Testis expressed transcript, Y-linked 8 |
LINC00130, NCRNA00130, TTY8 |
Curated: N/A
Unreviewed: N/A
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190862
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Testis expressed transcript, Y-linked 8B |
NCRNA00217, TTTY8 |
Curated: N/A
Unreviewed: N/A
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190863
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Testis expressed transcript, Y-linked 9A |
NCRNA00131, TTTY9, TTY9 |
Curated: N/A
Unreviewed: N/A
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190864
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Testis expressed transcript, Y-linked 9B |
NCRNA00132, TTTY9, TTTY9A, TTY9 |
Curated: N/A
Unreviewed: N/A
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190865
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Tweety family member 1 |
- |
Curated: Idiopathic pulmonary fibrosis
Unreviewed: Brain Neoplasms, Breast Cancer, Breast Carcinoma, Glioma, Malignant Neoplasm, Neoplasms, Pulmonary Fibrosis, Strabismus, Triple negative breast cancer
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190866
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Tweety family member 2 |
C17orf29 |
Curated: Hearing loss
Unreviewed: Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal Neoplasms, Hypertension, Kidney Cancer, Malignant Neoplasm, Osteosarcoma, Renal Carcinoma
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190867
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|
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Tweety family member 3 |
- |
Curated: Cerebral amyloid angiopathy, Schizophrenia
Unreviewed: Breast neoplasm, Glioblastoma, Thyroid cancer, Turner syndrome, Urinary bladder neoplasms
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190868
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|
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TUB bipartite transcription factor |
RDOB, rd5 |
Curated: Autism, Coronary artery disease, Essential tremor, Hearing loss, Lung cancer, Retinitis pigmentosa
Unreviewed: Astigmatism, Breast Cancer, Breast Carcinoma, Cataract, Ciliopathy, Colonic neoplasm, Cone dystrophy, Congenital Hypoplasia Of Penis, Deafness, Dermatologic Disorders, Diabetes Mellitus, Diabetes mellitus, type 2, Glaucoma, Glioblastoma, Hearing Loss, Hyperinsulinism, Hypogonadism, Keratoconus, Leber Congenital Amaurosis, Malignant Neoplasm, Mental retardation, Metabolic Syndrome, Myopia, Nystagmus, Obesity, Optic Atrophy, Optic Neuropathy, Retinal degeneration, Retinal detachment, Retinal Dystrophy, RETINAL DYSTROPHY AND OBESITY, Retinitis Pigmentosa, Rod-cone dystrophy, Squamous cell carcinoma
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190869
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TUB antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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190870
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Tubulin alpha 1a |
B-ALPHA-1, LIS3, TUBA3 |
Curated: 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 syndrome
Unreviewed: Acquired Porencephaly, Agenesis Of Corpus Callosum, Agyria, Amyotrophic Lateral Sclerosis, Aplastic anemia, Basal ganglia disease, Behavior Disorders, Brain disease, Brain malformation, Brain stem neoplasms, Cerebellar agenesis, Cerebellar diseases, Cerebellar Hypoplasia, Congenital Cataract, Congenital Microcephaly, Congenital Porencephaly, Corpus callosum agenesis, Developmental Delay, Developmental disability, Diabetes, Diabetes Mellitus, Diabetic neuropathy, Disorders of sex development, Dysmorphic Features, Epilepsy, Hirschsprung Disease, Histiocytosis, Hydranencephaly, Hydrocephalus, Hypoplasia Of Corpus Callosum, Hypoplasia Of The Optic Nerve, Inclusion Body Myopathy With Paget Disease And Frontotemporal Dementia, Infertility, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Macular corneal dystrophy, Malformation of cortical development, Mental retardation, Microlissencephaly, Microphthalmos, Motor delay, Movement Disorders, Multiple Congenital Anomalies, Multiple sclerosis, Myocardial Ischemia, Myoclonic epilepsy, Nervous System Disorder, Neuronal Heterotopia, Pachygyria, Paget disease, Parkinson disease, Polymicrogyria, Porencephaly, Prostatic neoplasm, Retinopathy, Rheumatoid arthritis, Scoliosis, Septo-Optic Dysplasia, Spastic Quadriplegia, Stomach neoplasms, Trichohepatoenteric Syndrome, Tubulinopathy-Associated Dysgyria, Uranostaphyloschisis
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