Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14101 to 14110 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14101
TRNA methyltransferase 1L
C1orf25, MST070, MSTP070, TRM1L, bG120K12.3
Metabolic syndrome, Diabetes mellitus type 2

14102
TRNA methyltransferase 2A
HTF9C
Schizophrenia

14103
TRNA methyltransferase 2B
CXorf34, dJ341D10.3
Neurodevelopmental disorder

14104
TRNA methyltransferase 44 homolog
C4orf23, METTL19, TRM44
Systemic lupus erythematosus

14105
TRNA methyltransferase 5
COXPD26, KIAA1393, PNSED, TRM5
Combined oxidative phosphorylation deficiency, Mitochondrial disease, Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay

14106
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

14107
TRNA methyltransferase 61B
-
Breast cancer, Triple negative breast cancer

14108
TRNA methyltransferase 9B (putative)
C8orf79, KIAA1456, TRM9L, hTRM9L
Attention deficit hyperactivity disorder, Colorectal cancer, Gastric cancer, Iga nephropathy, Lung cancer, Migraine, Oligodendroglioma, Post-traumatic stress disorder, Schizophrenia, Substance abuse, Diabetes mellitus type 2

14109
TRNA mitochondrial 2-thiouridylase
LCAL3, MTO2, MTU1, TRMT, TRMT1
Infantile liver failure, Aminoglycoside-induced deafness, Deafness, aminoglycoside-induced, Leigh syndrome, Liver failure, Mitochondrial disease

14110
TRNA nucleotidyl transferase 1
CCA1, CGI-47, MtCCA, RPEM, SIFD
Sideroblastic anemia with b-cell immunodeficiency, Intellectual developmental disorder, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa and erythrocytic microcytosis, Sideroblastic anemia