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"
961 to 970 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

961
TRNA methyltransferase 10A
HEL-S-88, MSSGM, MSSGM1, RG9MTD2, TRM10
Congenital neurologic anomalies, Liver disease, Microcephaly, Nonalcoholic fatty liver disease, Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome

962
TRNA methyltransferase 10C, mitochondrial RNase P subunit
COXPD30, HNYA, MRPP1, RG9MTD1
Asthma, Eczema, Basal cell carcinoma, Combined oxidative phosphorylation deficiency, Major depressive disorder, Mitochondrial disease

963
TRNA methyltransferase 11
C6orf75, MDS024, TRM11, TRMT11-1
Androgenetic alopecia, Breast neoplasms, Non-small-cell lung carcinoma, Colonic neoplasms, Esophageal neoplasms, Glioblastoma, Liver neoplasms, Lymphatic metastasis, Ovarian neoplasms

964
TRNA methyltransferase 1L
C1orf25, MST070, MSTP070, TRM1L, bG120K12.3
Metabolic syndrome, Diabetes mellitus type 2

965
TRNA methyltransferase 2A
HTF9C
Schizophrenia

966
TRNA methyltransferase 2B
CXorf34, dJ341D10.3
Neurodevelopmental disorder

967
TRNA methyltransferase 44 homolog
C4orf23, METTL19, TRM44
Systemic lupus erythematosus

968
TRNA methyltransferase 5
COXPD26, KIAA1393, PNSED, TRM5
Combined oxidative phosphorylation deficiency, Mitochondrial disease, Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay

969
TRNA methyltransferase 61A
C14orf172, GCD14, Gcd14p, TRM61, hTRM61
Attention deficit hyperactivity disorder, Autism, Basal cell carcinoma, Bone fracture, Cornelia de lange syndrome, Hypertension, Insomnia, Major depressive disorder, Schizophrenia, Diabetes mellitus type 2

970
TRNA methyltransferase 61B
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Breast cancer, Triple negative breast cancer