MT-TT mitochondrially encoded tRNA threonine

Gene ID: 4576, updated on 10-Oct-2023
Gene type: tRNA
Also known as: MTTT; TRNT

Associated conditions

See all available tests in GTR for this gene

Description	Tests
Lethal infantile mitochondrial myopathy MedGen: C1838876OMIM: 551000GeneReviews: Primary Mitochondrial Disorders Overview	See labs
Parkinson disease, mitochondrial MedGen: C1838867OMIM: 556500GeneReviews: Parkinson Disease Overview	See labs

Genomic context

Sequence:: Chromosome: MT; NC_012920.1 (15888..15953)

Total number of exons:: 0

Genomic Sequence

Go to nucleotideGraphics FASTA GenBank

Variation

Resource	Links for this gene
ClinVar	Variants reported to ClinVar
dbVar	Studies and variants
SNP	Variation Viewer for MT-TT variants
Genome viewer	Explore NCBI-annotated and select non-NCBI annotated genome assemblies

Links

ClinVar
Related medical variations
dbVar
Link from Gene to dbVar
MedGen
Related information in MedGen
OMIM
Link to related OMIM entry
PubMed (OMIM)
Gene links to PubMed derived from omim_pubmed_cited links
Variation Viewer
Related Variants

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