Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Diseases
Genes
Construct Expressed Component
Construct Knockdown Component
Construct Regulatory Region
Allele/Variant Diseases: combined oxidative phosphorylation deficiency
mldrKK108043
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0235330
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 54
Variant Name: Not Available
RNaseZF155L.ΔPAM.Tag:V5
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0391503
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 17, cardiomyopathy
Variant Name: Not Available
Mto1Gt(G019A03)Wrst
(Mus musculus)Allele/Variant
Source: MGI:4336382
Genes: Mto1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency
Variant Name: Not Available
CG4743null
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0367248
Genes: CG4743 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 28
Variant Name: Not Available
RNaseZU6.3xsgRNA
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0391501
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 17, cardiomyopathy
Variant Name: Not Available
RNaseZT494I.ΔPAM.Tag:V5
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0391504
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 17, cardiomyopathy
Variant Name: Not Available
CG4743KK102952
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0232119
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 28
Variant Name: Not Available
RNaseZHCM1.Tag:V5
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0369460
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 17
Variant Name: Not Available
RNaseZHCM2.Tag:V5
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0369461
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 17
Variant Name: Not Available
rswlGD12447
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0204587
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: combined oxidative phosphorylation deficiency 30
Variant Name: Not Available
CG4743I172G
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0367250
Genes: CG4743 (Dme)
Synonyms: Not Available
Variant Type: MNV
Molecular Consequence: missense_variant
Diseases: combined oxidative phosphorylation deficiency 28
Variant Name: Not Available
CG4743A123V
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0367249
Genes: CG4743 (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: combined oxidative phosphorylation deficiency 28
Variant Name: Not Available
RNaseZED24
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0291000
Genes: RNaseZ (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: 5_prime_UTR_variant, start_lost, splice_donor_variant, splice_acceptor_variant, intron_variant
Diseases: combined oxidative phosphorylation deficiency 17
Variant Name: Not Available
CG4743P223L
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0367251
Genes: CG4743 (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: combined oxidative phosphorylation deficiency 28
Variant Name: Not Available