Source: ALL

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Chronic progressive external ophthalmoplegia
disease 0.400 None 1.000 1 0 2013 2013
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency
disease 0.400 None 0 1
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 2 (finding)
phenotype 0.100 None 0 1
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Progressive proximal muscle weakness
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Restrictive deficit on pulmonary function testing
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay
disease 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C0476273
Disease: Respiratory distress
Respiratory distress
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C0427055
Disease: Facial Paresis
Facial Paresis
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C0341703
Disease: Adult Fanconi syndrome
Adult Fanconi syndrome
disease 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Muscle abnormality related to mitochondrial dysfunction
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Increased hepatocellular lipid droplets
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Cytochrome C oxidase-negative muscle fibers
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Abnormal mitochondria in muscle tissue
disease 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Increased intramyocellular lipid droplets
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C4016605
Disease: OPHTHALMOPLEGIA, ISOLATED
OPHTHALMOPLEGIA, ISOLATED
disease 0.100 None 0 2
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
Respiratory insufficiency due to muscle weakness
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers
phenotype 0.100 None 0 0
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
tRNA 0.682 0.577
CUI: C2673700
Disease: Brisk reflexes
Brisk reflexes
phenotype 0.100 None 0 0