Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "T"
191 to 200 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

191
Transcobalamin 2
D22S676, D22S750, II, TC, TC II, TC-2, TC2, TCII
Alzheimer disease, Megaloblastic anemia, Autism, Cleft lip, Colorectal neoplasms, Complete unilateral cleft lip, Deficiency anemia, Esophageal squamous cell carcinoma, Moyamoya disease, Pancytopenia, Parkinson disease, Prostatic neoplasms, Transcobalamin deficiency, Diabetes mellitus type 2, Vitamin b deficiency
View all (2 more)

192
Treacle ribosome biogenesis factor 1
MFD1, TCS, TCS1, treacle
Craniofacial abnormalities, Desbuquois syndrome, Glioma, Hearing impairment, Mandibulofacial dysostosis, Treacher collins syndrome

193
T-complex 1
CCT-alpha, CCT1, CCTa, D6S230E, IDDPMGS, TCP-1-alpha
Intellectual developmental disorder seizures polymicrogyria, Neurodevelopmental disorder, Prostatic neoplasms

194
T-complex 10 like
C21orf77, LINC00846, PRED77, TCP10A-1, TCP10A-2
Gastritis, Hepatocellular carcinoma, Scoliosis

195
T-complex 11
D6S230E, FPPR
Asthma, Rhinosinusitis, Graves disease, Hyperpituitarism, Insomnia, Irritable bowel syndrome, Osteoarthritis, Respiratory system disease, Sinusitis, Systemic lupus erythematosus

196
T-complex 11 like 1
dJ85M6.3
Omphalocele exstrophy imperforate anus, Diabetes mellitus type 2

197
T-complex 11 like 2
-
Schizophrenia

198
Tectonic family member 1
JBTS13, TECT1
Atrial fibrillation, Developmental disability, Aplasia of the vermis, Global developmental delay, Joubert syndrome, Meckel-gruber syndrome

199
Tectonic family member 2
C12orf38, JBTS24, MKS8, TECT2
Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Joubert syndrome, Meckel-gruber syndrome

200
Tectonic family member 3
C10orf61, JBTS18, OFD4, TECT3
Ciliopathy, Desbuquois syndrome, Diverticular disease, Aplasia of the vermis, Joubert syndrome, Meckel-gruber syndrome, Orofaciodigital syndrome