261
|
|
|
Tubulin folding cofactor A pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
262
|
|
|
Tubulin folding cofactor A pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
263
|
|
|
Tubulin folding cofactor A pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
264
|
|
|
Tubulin folding cofactor B |
CG22, CKAP1, CKAPI |
Curated: N/A
Unreviewed: Amyotrophic Lateral Sclerosis, Schizophrenia, Trigeminal neuralgia
|
265
|
|
|
Tubulin folding cofactor C |
CFC |
Curated: Bipolar disorder, Stroke
Unreviewed: Breast Carcinoma, Congenital Heart Disease, Costello syndrome, Forebrain Defects, Hyperemia, Leukemia, Myelodysplastic Syndrome, Myeloid Leukemia, Neoplasms, Psoriasis
|
266
|
|
|
TBCC domain containing 1 |
- |
Curated: Male infertility single gene azoospermia
Unreviewed: N/A
|
267
|
|
|
Tubulin folding cofactor D |
PEBAT, SSD-1, tfcD |
Curated: Astrocytoma, Central nervous system cancer, Coronary artery disease, Degenerative disorder, Developmental disability, Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome, Glioblastoma, Glioma, Intellectual developmental disorder, Cortical development malformation, Microcephaly, Neurodegenerative disorder, Optic atrophy, Seborrhea-like dermatitis with psoriasiform elements, Seborrheic keratosis, Seizures, Thiel-behnke corneal dystrophy, Diabetes mellitus type 2
Unreviewed: Afibrinogenemia, Arthrogryposis multiplex congenita, Asthma, Atrophy, Bowel incontinence, Brain disease, Brainstem Atrophy, Cataplexy, Cerebellar atrophy, Cerebellar diseases, Cerebellar hypoplasia, Cerebral cortical atrophy, Clonic Seizures, Colorectal neoplasm, Congenital Microcephaly, Congenital Pectus Carinatum, Congenital Pectus Excavatum, Corneal Dystrophy, Corpus callosum agenesis, Cortical Dysplasia, Degenerative Diseases, Central Nervous System, Demyelinating diseases, Development Disorder, Developmental Delay, Developmental dysplasia of the hip, Developmental regression, Diffuse Brain Atrophy-Microcephaly-Muscle Weakness-Optic Atrophy Syndrome, Distal myopathy, Dysphagia, Encephalopathy With Brain Atrophy And Thin Corpus Callosum, Epilepsy, Epileptic encephalopathy, Febrile seizures, Fibrinogen Deficiency, Hereditary Motor Neuropathy, Hypofibrinogenemia, Hypoplasia Of Corpus Callosum, Hypotonic seizures, Jacksonian Seizure, Macrotia, Malformation of cortical development, Mental retardation, Micrognathism, Microlissencephaly, Neurodegenerative Disorders, Neurogenic Urinary Bladder, Optic Atrophy, Plagiocephaly, Quadriplegia, Respiratory Failure, Schizophrenia, Scoliosis, Seizure, Spastic Quadriplegia, Spinal Muscular Atrophy, Stereotyped Behavior, Tourette syndrome, West Syndrome
|
268
|
|
|
Tubulin folding cofactor E |
HRD, KCS, KCS1, PEAMO, pac2 |
Curated: Kenny-caffey syndrome, Craniofacial abnormalities, Desbuquois syndrome, Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome, Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome, Obesity, Oligodendroglioma, Osteosclerosis, Pituitary stalk interruption syndrome, Sanjad-sakati syndrome, Diabetes mellitus type 2, encephalopathy, progressive, with amyotrophy and optic atrophy
Unreviewed: Anarthria Speech Disorder, Anemia, Astigmatism, Brain disease, Cerebellar atrophy, Congenital abnormalities, Congenital hypoparathyroidism, Congenital Hypoplasia Of Penis, Congenital Muscular Dystrophy-Dystroglycanopathy With Brain And Eye Anomalies, Cryptorchidism, Defect Of Skull Ossification, Developmental Delay, Developmental regression, Disorders of sex development, Distal amyotrophy, Distal Spinal Muscular Atrophy, Dry Eye Syndromes, Dwarfism, Dysarthria, Dysmorphic Features, Dysmorphism, Encephalopathy, With Amyotrophy And Optic Atrophy, Encephalopathy-Spastic Ataxia-Distal Spinal Muscular Atrophy Syndrome, Epileptic encephalopathy, Facial dysmorphism, Facial dysmorphism syndrome, Frontal bossing, Growth disorder, Hyperphosphatemia, Hypocalcemic seizures, Hypocalcemic tetany, Hypoparathyroidism, Hypoparathyroidism-retardation-dysmorphism syndrome, Hypoplasia Of Corpus Callosum, Intellectual developmental disorder, Intestinal Obstruction, Isolated Somatotropin Deficiency, Kenny-Caffey Syndrome, Keratoconjunctivitis Sicca, Leukemia, Malignant Neoplasm, Mental retardation, Microcephaly, Micrognathism, Monocytic Leukemia, Motor Neuron Disease, Multiple Congenital Anomalies, Myopathy, Neoplasms, Optic Atrophy, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Paroxysmal nocturnal hemoglobinuria, Penis Agenesis, Peripheral axonal neuropathy, Polyglandular autoimmune syndrome, Posteriorly Rotated Ear, Scoliosis, Severe combined immunodeficiency, Somatotropin Deficiency, Spastic Ataxia, Spastic Quadriplegia, Spastic tetraparesis, Spinal Muscular Atrophy, Stenosis of the medullary cavity of the long bones, Trichohepatoenteric Syndrome, Triple Negative Breast Neoplasms
|
269
|
|
|
Tubulin folding cofactor E like |
El, LRRC35 |
Curated: Hearing loss
Unreviewed: Adenocarcinoma, Brachydactyly, Neoplasms, Neuroblastoma, Retinoblastoma
|
270
|
|
|
TBCEL-TECTA readthrough |
- |
Curated: Autoimmune musculoskeletal system disorder, Congenital ear anomaly, Congenital sensorineural hearing loss, Deafness, Hearing loss, Meniere disease, Nonsyndromic hearing loss, Systemic lupus erythematosus
Unreviewed: N/A
|