391
|
|
|
T-complex 1 pseudogene 3 |
CCT1-1P, TCP1L3 |
Curated: N/A
Unreviewed: N/A
|
392
|
|
|
- |
- |
Curated: N/A
Unreviewed: Hypothyroidism, Thyroid dyshormonogenesis
|
393
|
|
|
T cell leukemia translocation altered |
- |
Curated: N/A
Unreviewed: Crohn Disease, Hematologic neoplasm, Hyperuricemia, Myeloid leukemia, Pancreatic neoplasm, Schizophrenia, T-cell leukemia
|
394
|
|
|
Tectonic family member 1 |
JBTS13, TECT1 |
Curated: Atrial fibrillation, Developmental disability, Aplasia of the vermis, Global developmental delay, Joubert syndrome, Meckel-gruber syndrome
Unreviewed: Cerebellar vermis agenesis, Ciliopathies, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Developmental Delay, Disorder Of Eye, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Glioblastoma, Glioma, Hirschsprung Disease, Holoprosencephaly, Hydrocephalus, Joubert Syndrome, Lung carcinoma, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Neoplasms, Nystagmus, Occipital Encephalocele, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Oral cleft, Orofaciodigital syndrome, Pachygyria, Pancreatic cancer, Pancreatic carcinoma, Polydactyly Of Toes, Polymicrogyria, Prostate cancer, Prostatic neoplasm, Ptosis, Scoliosis, Situs Inversus, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm
|
395
|
|
|
Tectonic family member 2 |
C12orf38, JBTS24, MKS8, TECT2 |
Curated: Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Joubert syndrome, Meckel-gruber syndrome, joubert syndrome 24
Unreviewed: Anencephaly, Asplenia, Cataract, Cerebellar Hypoplasia, Cerebellar vermis agenesis, Ciliopathies, Ciliopathy, Congenital Cerebral Hernia, Congenital Clubfoot, Congenital Coloboma Of Iris, Congenital Hepatic Fibrosis, Cryptorchidism, Cystic liver disease, Dandy-Walker Syndrome, Developmental Delay, Disorder Of Eye, Double Ureter, Fibrosis Of Pancreas, Foot Polydactyly, Hirschsprung Disease, Hydrocephalus, Hyperopia, Joubert Syndrome, Lobar Holoprosencephaly, Male Pseudohermaphroditism, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Neoplasms, Nephronophthisis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Oral cleft, Ovarian cancer, Pachygyria, Pancreatic Cyst, Polycystic liver disease, Polydactyly, Polydactyly Of Toes, Polymicrogyria, Postaxial hand polydactyly, Ptosis, Sclerocornea, Scoliosis, Situs Inversus, Strabismus, Syndromic microphthalmia, Talipes, True Hermaphroditism, Urethral atresia
|
396
|
|
|
Tectonic family member 3 |
C10orf61, JBTS18, OFD4, TECT3 |
Curated: Ciliopathy, Desbuquois syndrome, Diverticular disease, Aplasia of the vermis, Joubert syndrome, Meckel-gruber syndrome, Orofaciodigital syndrome
Unreviewed: Acquired Kyphoscoliosis, Acquired Porencephaly, Addison`s Disease, Bone Disease, Brachydactyly, Brain disease, Cerebellar vermis agenesis, Cerebral Atrophy, Cerebral cortical hemiatrophy, Choanal Atresia, Ciliopathies, Clinodactyly, Congenital Atresia Of Rectum, Congenital Camptodactyly, Congenital Epicanthus, Congenital heart defect, Congenital heart defects, Congenital kyphoscoliosis, Congenital Pectus Excavatum, Cryptorchidism, Developmental Delay, Disorder Of Eye, Dwarfism, Esotropia, Frontal bossing, Hamartoma, Hearing Loss, High palate, Holoprosencephaly, Horseshoe Kidney, Hypothalamic Hamartomas, Imperforate anus, Joubert Syndrome, Kidney disease, Laryngomalacia, Malformation of cortical development, Mental retardation, Microcephaly, Micrognathism, Micromelia, Monorchism, Neural Tube Defect, Nystagmus, Osteofibrous Dysplasia, Polydactyly, Polydactyly Of Toes, Porencephalic cyst, Postaxial hand polydactyly, Posteriorly Rotated Ear, Proptosis, Pulmonary hypoplasia, Radial Polydactyly, Renal agenesis, Short Rib-Polydactyly Syndrome, Specific Learning Disorder, Subcortical cerebral atrophy, Submucosal cleft palate, Syndactyly, Syndactyly of fingers, Syndactyly Of The Toes, Ventricular septal defect
|
397
|
|
|
Thymine DNA glycosylase |
hTDG |
Curated: N/A
Unreviewed: Adrenocortical carcinoma, Breast Cancer, Breast Carcinoma, Breast neoplasm, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Ependymoma, Esophageal squamous cell carcinoma, Hepatocellular carcinoma, Leukemia, Lung Neoplasms, Malignant Neoplasm, Medulloblastoma, Melanoma, Multiple myeloma, Myelodysplastic Syndrome, Neoplasms, Pancreatic cancer, Pancreatic carcinoma, Rectal Carcinoma, Skin cancer, Skin neoplasm, Stomach Carcinoma, Stomach Neoplasms, Systemic lupus erythematosus, Urinary bladder neoplasms, Uterine disease, Xeroderma Pigmentosum
|
398
|
|
|
Thymine-DNA glycosylase pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
399
|
|
|
L-threonine dehydrogenase (pseudogene) |
SDR14E1P |
Curated: N/A
Unreviewed: N/A
|
400
|
|
|
TDH antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|