Gene: CYTB
Alternate names for this Gene:
Gene Summary:
Gene is located in Chromosome:
Location in Chromosome :
Description of this Gene:
Type of Gene:
Gene: ND6
Alternate names for this Gene:
Gene Summary:
Gene is located in Chromosome:
Location in Chromosome :
Description of this Gene:
Type of Gene:
Gene: TRNT
Alternate names for this Gene:
Gene Summary:
Gene is located in Chromosome:
Location in Chromosome :
Description of this Gene:
Type of Gene:
rs1556424691 in
CYTB;ND6;TRNT gene and
Abnormal color vision
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
rs1556424691 in
CYTB;ND6;TRNT gene and
Abnormality of the cerebral cortex
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
rs1556424691 in
CYTB;ND6;TRNT gene and
Cerebral cortical atrophy
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
rs1556424691 in
CYTB;ND6;TRNT gene and
Hyperreflexia in upper limbs
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
rs1556424691 in
CYTB;ND6;TRNT gene and
Increased CSF lactate
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
rs1556424691 in
CYTB;ND6;TRNT gene and
Memory impairment
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
rs1556424691 in
CYTB;ND6;TRNT gene and
Mental deterioration
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
rs1556424691 in
CYTB;ND6;TRNT gene and
Mitochondrial Diseases
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
rs1556424691 in
CYTB;ND6;TRNT gene and
Muscle Weakness
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
rs1556424691 in
CYTB;ND6;TRNT gene and
Secondary physiologic amenorrhea
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
rs1556424691 in
CYTB;ND6;TRNT gene and
Seizures
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
rs1556424691 in
CYTB;ND6;TRNT gene and
Seizures, Focal
PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.
PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.
PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.