Gen
MT-TQ
mitochondrially encoded tRNA-Gln (CAA/G)
- HGNC 7495(åbnes i en ny fane)
- Ensembl-gen ENSG00000210107(åbnes i en ny fane)
- NCBI Gene 4572(åbnes i en ny fane)
Oversigt
- Cytogenetisk placering
- mitochondria
- Også kendt som
- trnQ
- Tidligere symboler
- MTTQ
- Lokustype
- RNA, transfer
ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
Læs MT-TQ og resten af dit genom med én test.
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Bestil min Genome TestKurerede rapporter relevant for dette gen
Ingen Genome Test-rapport læser MT-TQ endnu. Testen sekventerer hele dit genom, så dine data omfatter det alligevel.
Træk knyttet til MT-TQ
Human Phenotype Ontology angiver disse som kendetegn ved de sjældne tilstande, MT-TQ kan forårsage. Hvert træks side viser de andre gener, der er knyttet til det.
Abnormality of the nervous system
- Abnormality of movement
- Absent/small cerebral white matter
- Ataxia
- Dementia
- Difficulty finding words
- EEG abnormality
- Epilepsy
- Generalized myoclonic seizure
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- Migraine
- Widened cerebral subarachnoid space
- Abnormal gait
- Anxiety
- Cognitive impairment
- Depression
- Encephalopathy
- Fluctuations in consciousness
- Grand mal seizures
- Impaired visuospatial constructive cognition
- Jerking
- Memory impairment
- Peripheral neuropathy
- Psychosis
- Recurrent paroxysmal headache
- Seizure affecting one half of brain
- Short attention span
- Specific learning disability
- Weakness of one side of body
- Abnormal central motor function
- Agenesis of corpus callosum
- Bipolar disorder
- Brain degeneration
- Decrease in size of the outer layer of the brain due to loss of brain cells
- Distal peripheral sensory neuropathy
- Disturbances of consciousness
- Elevated brain lactate level by MRS
- Global developmental delay
- Mixed demyelinating and axonal polyneuropathy
- Motor delay
- Nerve damage causing decreased feeling and movement
- Peripheral axonal neuropathy
- Personality changes
- Psychotic mentation
- Stuttering
- Underdevelopment of part of brain called corpus callosum
Laboratory abnormality
- Higher than normal levels of lactate in blood
- Increased lactate in body
- Diabetes mellitus
- Increased CSF lactate
- Increased CSF protein concentration
- Fever
- High urine protein levels
- Noninsulin-dependent diabetes
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Eksterne links
Hvor oplysningerne kommer fra
- HGNC: genets symbol, navn, andre symboler og placering.
- Human Phenotype Ontology, version 2026-09-01: de træk, der er knyttet til genet. Læs mere på hpo.jax.org.
Citér denne side
Dante Labs. (u.d.). MT-TQ-genet: mitochondrially encoded tRNA-Gln (CAA/G). Hentet 17. oktober 2026, fra https://dantelabs.com/da/genes/mt-tq
Dante Labs. MT-TQ-genet: mitochondrially encoded tRNA-Gln (CAA/G) [Internet]. [citeret 17. oktober 2026]. Tilgængelig fra: https://dantelabs.com/da/genes/mt-tq
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Fra 449 $Gratis forsendelse · Resultater på 6–8 uger