MT-TT

Chr mitochondria

mitochondrially encoded tRNA-Thr (ACN)

Aliases:: trnT

OMIM: 590090 ↗NCBI: 4576 ↗Ensembl ↗

Annotations refreshed 9 hours ago.

Predicted protein structure

No predicted 3D structure for MT-TT. Non-coding genes and pseudogenes typically have no protein product.

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

Likely inborn error of metabolism
MITOCHONDRIAL
Mitochondrial disorders
MITOCHONDRIAL
Childhood onset dystonia, chorea or related movement disorder
MITOCHONDRIAL

Disease associations (Open Targets)

inborn mitochondrial metabolism disorder
0.51
mitochondrial disease
0.51
MERRF syndrome
0.46
MERRF
0.46
Leber hereditary optic neuropathy
0.46
breast carcinoma
0.04
ulcerative colitis
0.02
sclerosing cholangitis
0.00
infection
0.00
lethal infantile mitochondrial myopathy
0.00

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.