Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
751 to 760 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

751
Tumor suppressor candidate 3
D8S1992, M33, MRT22, MRT7, MagT2, N33, OST3A, SLC58A2
Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Polymicrogyria
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752
TNFAIP3 interacting protein 3
ABIN-3, LIND
Breast cancer, Breast carcinoma

753
Transient receptor potential cation channel subfamily M member 3
CTRCT50, GON-2, LTRPC3, MLSN2, NEDFSS
Autism, Coronary artery disease, Developmental delay, Exudative macular degeneration, Geographic atrophy, Age-related macular degeneration, Mental retardation, Non-syndromic intellectual disability, Retinal dystrophy and iris coloboma with or without congenital cataract, Thyroid nodule

754
Tripartite motif containing 46
GENEY, TRIFIC
Breast carcinoma, Gout, Gouty arthritis, Leukemia

755
THO complex subunit 7
NIF3L1BP1, fSAP24, hTREX30
Schizophrenia

756
Tubulin epsilon and delta complex 2
C16orf59
Liver carcinoma

757
TELO2 interacting protein 2
C8orf41, MRT39
Acquired kyphoscoliosis, Congenital kyphoscoliosis, Developmental delay, Dwarfism, Mental retardation, Intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome, Macrotia, Microcephaly, Stereotyped behavior, Strabismus, Synophrys

758
Transmembrane protein 254
C10orf57, bA369J21.6
Chronic obstructive pulmonary disease

759
Threonyl-tRNA synthetase 2, mitochondrial
COXPD21, TARSL1, thrRS
Combined oxidative phosphorylation deficiency, Developmental delay, Fatty liver, Hypoplasia of corpus callosum

760
TLR adaptor interacting with endolysosomal SLC15A4
CXorf21
Lupus erythematosus