Name

abnormal mitochondrial shape Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal mitochondrial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal mitochondrial shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal facial shape Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal facial shape Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal facial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal shape of the palpebral fissure Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal shape of the palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal shape of the radius Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal shape of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal shape of the frontal region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal shape of the frontal region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal shape of the occiput Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal shape of the occiput phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal auditory brainstem response waveform shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal a wave shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal a wave shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal head shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal head shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lip shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lip shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ear shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ear shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft melanin granule shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shaft melanin granule shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal b-wave shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal b-wave shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal thoracic cage shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal thoracic cage shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal somite shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal somite shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

shapedependent Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term shapedependent in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

shape Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term shape in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

shaped Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term shaped in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

shapes Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term shapes in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

regulation of cell shape Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cell shape biological process from the curated GO Biological Process Annotations dataset.

metanephric s-shaped body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the metanephric s-shaped body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

comma-shaped body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the comma-shaped body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of metanephric s-shaped body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of metanephric s-shaped body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

s-shaped body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the s-shaped body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of metanephric comma-shaped body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of metanephric comma-shaped body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of metanephric s-shaped body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of metanephric s-shaped body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

establishment or maintenance of cell polarity regulating cell shape Gene Set

From GO Biological Process Annotations

genes participating in the establishment or maintenance of cell polarity regulating cell shape biological process from the curated GO Biological Process Annotations dataset.

regulation of embryonic cell shape Gene Set

From GO Biological Process Annotations

genes participating in the regulation of embryonic cell shape biological process from the curated GO Biological Process Annotations dataset.

regulation of metanephric comma-shaped body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of metanephric comma-shaped body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

metanephric comma-shaped body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the metanephric comma-shaped body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

u-shaped upper lip vermilion Gene Set

From HPO Gene-Disease Associations

genes associated with the u-shaped upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

y-shaped metacarpals Gene Set

From HPO Gene-Disease Associations

genes associated with the y-shaped metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dumbbell-shaped long bone Gene Set

From HPO Gene-Disease Associations

genes associated with the dumbbell-shaped long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

almond-shaped palpebral fissure Gene Set

From HPO Gene-Disease Associations

genes associated with the almond-shaped palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

club-shaped proximal femur Gene Set

From HPO Gene-Disease Associations

genes associated with the club-shaped proximal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

j-shaped sella turcica Gene Set

From HPO Gene-Disease Associations

genes associated with the j-shaped sella turcica phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

barrel-shaped chest Gene Set

From HPO Gene-Disease Associations

genes associated with the barrel-shaped chest phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pear-shaped vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the pear-shaped vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped proximal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dagger-shaped pulp calcifications Gene Set

From HPO Gene-Disease Associations

genes associated with the dagger-shaped pulp calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped middle phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped epiphyses of phalanges 2 to 5 Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of phalanges 2 to 5 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cuboid-shaped vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the cuboid-shaped vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped phalanges of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped phalanges of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lens shape Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of lens shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial shape deformation Gene Set

From HPO Gene-Disease Associations

genes associated with the facial shape deformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular-shaped open mouth Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular-shaped open mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peg-shaped maxillary lateral incisors Gene Set

From HPO Gene-Disease Associations

genes associated with the peg-shaped maxillary lateral incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bullet-shaped phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the bullet-shaped phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pear-shaped nose Gene Set

From HPO Gene-Disease Associations

genes associated with the pear-shaped nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thimble-shaped middle phalanges of hand Gene Set

From HPO Gene-Disease Associations

genes associated with the thimble-shaped middle phalanges of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subsarcolemmal accumulations of abnormally shaped mitochondria Gene Set

From HPO Gene-Disease Associations

genes associated with the subsarcolemmal accumulations of abnormally shaped mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped epiphysis of the 1st metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphysis of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dumbbell-shaped metaphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the dumbbell-shaped metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

screwdriver-shaped incisors Gene Set

From HPO Gene-Disease Associations

genes associated with the screwdriver-shaped incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tombstone-shaped proximal phalanges Gene Set

From HPO Gene-Disease Associations

genes associated with the tombstone-shaped proximal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chin with h-shaped crease Gene Set

From HPO Gene-Disease Associations

genes associated with the chin with h-shaped crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bell-shaped thorax Gene Set

From HPO Gene-Disease Associations

genes associated with the bell-shaped thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped phalanges of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

club-shaped distal femur Gene Set

From HPO Gene-Disease Associations

genes associated with the club-shaped distal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped capital femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormally shaped carpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormally shaped carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

halberd-shaped pelvis Gene Set

From HPO Gene-Disease Associations

genes associated with the halberd-shaped pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hump-shaped mound of bone in central and posterior portions of vertebral endplate Gene Set

From HPO Gene-Disease Associations

genes associated with the hump-shaped mound of bone in central and posterior portions of vertebral endplate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped proximal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dumbbell-shaped femur Gene Set

From HPO Gene-Disease Associations

genes associated with the dumbbell-shaped femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped metacarpal epiphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped metacarpal epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bullet-shaped middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the bullet-shaped middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of mouth shape Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of mouth shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ALIX V-shaped domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ALIX V-shaped domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

irregularly shaped pupil Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the irregularly shaped pupil phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cup-shaped ears Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cup-shaped ears phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

nail disorder, nonsyndromic congenital, 10, (claw-shaped nails) Gene Set

From OMIM Gene-Disease Associations

genes associated with the nail disorder, nonsyndromic congenital, 10, (claw-shaped nails) phenotype from the curated OMIM Gene-Disease Associations dataset.

abnormal mitochondrial morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal mitochondrial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal activity of mitochondrial respiratory chain Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal mitochondrial proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial chromosome morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial chromosome morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sperm mitochondrial sheath morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sperm mitochondrial sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial inner membrane morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial inner membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial crista morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial crista morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial atp synthesis coupled electron transport Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial atp synthesis coupled electron transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial matrix morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial matrix morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Mitochondrial diseases Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial diseases phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 4B, MNGIE type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 4B, MNGIE type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

RRM2B-related mitochondrial disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial phosphate carrier deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial phosphate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple mitochondrial dysfunctions syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple mitochondrial dysfunctions syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial pyruvate carrier deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial pyruvate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial trifunctional protein deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial trifunctional protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA-depletion syndrome 3, hepatocerebral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA-depletion syndrome 3, hepatocerebral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

mitochondrial envelope Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial envelope cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex ii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex ii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iv Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex iv cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex, catalytic core f(1) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial alpha-ketoglutarate dehydrogenase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial alpha-ketoglutarate dehydrogenase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex i Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex i cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of mitochondrial membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of mitochondrial membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial inner membrane peptidase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial endopeptidase clp complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial endopeptidase clp complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial fatty acid beta-oxidation multienzyme complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial fatty acid beta-oxidation multienzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial small ribosomal subunit Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

sperm mitochondrial sheath Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the sperm mitochondrial sheath cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial large ribosomal subunit Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex, coupling factor f(o) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial membrane part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial membrane part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial nucleoid Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial nucleoid cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial inner membrane presequence translocase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane presequence translocase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial ribosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial ribosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial outer membrane translocase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial outer membrane translocase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial crista Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial crista cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial degradosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial degradosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial permeability transition pore complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial permeability transition pore complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial intermembrane space protein transporter complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial intermembrane space cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex iii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial pyruvate dehydrogenase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial pyruvate dehydrogenase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase, catalytic core Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase, catalytic core cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial tricarboxylic acid cycle enzyme complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial tricarboxylic acid cycle enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial matrix Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial matrix cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cytoplasmic side of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cytoplasmic side of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial envelope Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial envelope cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iv Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex iv cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial outer membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial prohibitin complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial prohibitin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial alpha-ketoglutarate dehydrogenase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial alpha-ketoglutarate dehydrogenase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex i Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex i cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

integral component of mitochondrial membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the integral component of mitochondrial membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial inner membrane peptidase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial inner membrane peptidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial fatty acid beta-oxidation multienzyme complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial fatty acid beta-oxidation multienzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial small ribosomal subunit Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

3-methylcrotonyl-coa carboxylase complex, mitochondrial Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the 3-methylcrotonyl-coa carboxylase complex, mitochondrial cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

sperm mitochondrial sheath Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the sperm mitochondrial sheath cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial intermembrane space protein transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial large ribosomal subunit Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial membrane part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial membrane part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial ribonuclease p complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial ribonuclease p complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial nucleoid Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial nucleoid cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial inner membrane presequence translocase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial inner membrane presequence translocase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial ribosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial ribosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain supercomplex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain supercomplex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the intrinsic component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial outer membrane translocase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial outer membrane translocase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial crista Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial crista cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

integral component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the integral component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the intrinsic component of mitochondrial membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial derivative Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial derivative cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial degradosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial degradosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial cloud Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial cloud cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial proton-transporting atp synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial creatine kinase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial creatine kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial permeability transition pore complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial permeability transition pore complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial intermembrane space cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial crista junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial crista junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial electron transfer flavoprotein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial electron transfer flavoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex ii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex ii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial processing peptidase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial processing peptidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial inner membrane protein insertion complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial inner membrane protein insertion complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex iii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial pyruvate dehydrogenase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial pyruvate dehydrogenase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial tricarboxylic acid cycle enzyme complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial tricarboxylic acid cycle enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Respiratory chain complex I, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete NDUFAF1 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate VII/650kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate VII/650kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (lambda subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (lambda subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Cytochrome bc1-complex (EC 1.10.2.2), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Cytochrome bc1-complex (EC 1.10.2.2), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (gamma subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (gamma subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (beta subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (beta subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate IV/310kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate IV/310kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Succinate dehydrogenase complex II (EC 1.3.5.1), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Succinate dehydrogenase complex II (EC 1.3.5.1), mitochondrial protein complex from the CORUM Protein Complexes dataset.

55S ribosome, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the 55S ribosome, mitochondrial protein complex from the CORUM Protein Complexes dataset.

TIM (TIMM23, TIMM50) complex, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the TIM (TIMM23, TIMM50) complex, mitochondrial protein complex from the CORUM Protein Complexes dataset.

F1F0-ATP synthase (EC 3.6.3.14), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the F1F0-ATP synthase (EC 3.6.3.14), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Cytochrome c oxidase (EC 1.9.3.1), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Cytochrome c oxidase (EC 1.9.3.1), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete intermediate), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete intermediate), mitochondrial protein complex from the CORUM Protein Complexes dataset.

28S ribosomal subunit, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the 28S ribosomal subunit, mitochondrial protein complex from the CORUM Protein Complexes dataset.

TIM (TIMM17ab, TIMM23, TIMM44) complex, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the TIM (TIMM17ab, TIMM23, TIMM44) complex, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete intermediate ND1, ND2, ND3, CIA30 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete intermediate ND1, ND2, ND3, CIA30 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (holoenzyme), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (holoenzyme), mitochondrial protein complex from the CORUM Protein Complexes dataset.

39S ribosomal subunit, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the 39S ribosomal subunit, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate II/230kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate II/230kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

TIM (TIMM9, TIMM10) complex, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the TIM (TIMM9, TIMM10) complex, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Mitochondrial Phosphate Carrier Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Phosphate Carrier Deficiency from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE) from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Diseases from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Complex III Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Complex III Deficiency from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Myopathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Myopathies from the curated CTD Gene-Disease Associations dataset.

Mitochondrial neurogastrointestinal encephalopathy syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial neurogastrointestinal encephalopathy syndrome from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Encephalomyopathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Encephalomyopathies from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Complex II Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Complex II Deficiency from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.

MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE) from the curated CTD Gene-Disease Associations dataset.

Mitochondrial complex I deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial complex I deficiency from the curated CTD Gene-Disease Associations dataset.

mitochondrial myopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease mitochondrial myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

mitochondrial metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease mitochondrial metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

mitochondrial encephalomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mitochondrial encephalomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mitochondrial metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mitochondrial metabolism disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mitochondrial myopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal pseudo-obstruction; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal pseudo-obstruction; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; glaucoma, open-angle; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; glaucoma, open-angle; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mitochondrial diseases; nerve degeneration; presbycusis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mitochondrial diseases; nerve degeneration; presbycusis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mitochondrial myopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mitochondrial myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mitochondrial Gene Set

From GAD High Level Gene-Disease Associations

genes associated with the disease mitochondrial in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.

mitochondrial Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term mitochondrial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

mitochondrial respiratory chain complex ii biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex ii biogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial calcium ion concentration Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial calcium ion concentration biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial depolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial depolarization biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial depolarization Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial depolarization biological process from the curated GO Biological Process Annotations dataset.

protein insertion into mitochondrial membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein insertion into mitochondrial membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna 3'-end processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna 3'-end processing biological process from the curated GO Biological Process Annotations dataset.

regulation of protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations dataset.

mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

outer mitochondrial membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the outer mitochondrial membrane organization biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial intermembrane space Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial intermembrane space biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial membrane permeability Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial membrane permeability biological process from the curated GO Biological Process Annotations dataset.

mitochondrial threonyl-trna aminoacylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial threonyl-trna aminoacylation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iv biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iv biogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial dna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial dna metabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial electron transport, ubiquinol to cytochrome c Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial electron transport, ubiquinol to cytochrome c biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial depolarization Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial depolarization biological process from the curated GO Biological Process Annotations dataset.

mitochondrial membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial membrane organization biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna 3'-end processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna 3'-end processing biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna surveillance Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna surveillance biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna catabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial mrna surveillance Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial mrna surveillance biological process from the curated GO Biological Process Annotations dataset.

mitochondrial electron transport, nadh to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial electron transport, nadh to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial membrane potential Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial membrane potential biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna 3'-trailer cleavage, endonucleolytic Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna 3'-trailer cleavage, endonucleolytic biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna modification Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna modification biological process from the curated GO Biological Process Annotations dataset.

mitochondrial membrane fission Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial membrane fission biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna modification Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna modification biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex i assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex i assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial mrna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial mrna catabolic process biological process from the curated GO Biological Process Annotations dataset.

apoptotic mitochondrial changes Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic mitochondrial changes biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial matrix Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial matrix biological process from the curated GO Biological Process Annotations dataset.

mitochondrial electron transport, succinate to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial electron transport, succinate to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iv assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iv assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial pyrimidine nucleotide import Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial pyrimidine nucleotide import biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane permeabilization Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial outer membrane permeabilization biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial membrane permeability involved in apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial membrane permeability involved in apoptotic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial iron ion transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial iron ion transport biological process from the curated GO Biological Process Annotations dataset.

transcription initiation from mitochondrial promoter Gene Set

From GO Biological Process Annotations

genes participating in the transcription initiation from mitochondrial promoter biological process from the curated GO Biological Process Annotations dataset.

mitochondrial translational elongation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial translational elongation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial mrna polyadenylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial mrna polyadenylation biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane permeability Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane permeability biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial translation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial translation biological process from the curated GO Biological Process Annotations dataset.

protein insertion into mitochondrial membrane involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the protein insertion into mitochondrial membrane involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial rna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial rna catabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial calcium ion homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial calcium ion homeostasis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial membrane potential Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial membrane potential biological process from the curated GO Biological Process Annotations dataset.

mitochondrial calcium ion transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial calcium ion transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna metabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial pyruvate transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial pyruvate transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial protein catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial protein catabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial translational initiation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial translational initiation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial translational termination Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial translational termination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial electron transport, nadh to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial electron transport, nadh to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial membrane permeability involved in apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial membrane permeability involved in apoptotic process biological process from the curated GO Biological Process Annotations dataset.

stress-induced mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the stress-induced mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial translation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial translation biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial inner membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial inner membrane biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial membrane permeability Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial membrane permeability biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial dna replication Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial dna replication biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial electron transport, nadh to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial electron transport, nadh to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial rna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial rna catabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

mitochondrial ncrna surveillance Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial ncrna surveillance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial dna replication Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial dna replication biological process from the curated GO Biological Process Annotations dataset.

mitochondrial transmembrane transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial transmembrane transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial rna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial rna catabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial dna replication Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial dna replication biological process from the curated GO Biological Process Annotations dataset.

establishment of protein localization to mitochondrial membrane Gene Set

From GO Biological Process Annotations

genes participating in the establishment of protein localization to mitochondrial membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane permeability involved in apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane permeability involved in apoptotic process biological process from the curated GO Biological Process Annotations dataset.

dynamin polymerization involved in mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the dynamin polymerization involved in mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial dna replication Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial dna replication biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane potential biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna methylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna methylation biological process from the curated GO Biological Process Annotations dataset.

termination of mitochondrial transcription Gene Set

From GO Biological Process Annotations

genes participating in the termination of mitochondrial transcription biological process from the curated GO Biological Process Annotations dataset.

mitochondrial genome maintenance Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial genome maintenance biological process from the curated GO Biological Process Annotations dataset.

mitochondrial alanyl-trna aminoacylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial alanyl-trna aminoacylation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial fragmentation involved in apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial fragmentation involved in apoptotic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex ii assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex ii assembly biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial dna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial dna metabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial electron transport, nadh to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial electron transport, nadh to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

mitochondrial depolarization Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial depolarization biological process from the curated GO Biological Process Annotations dataset.

inner mitochondrial membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the inner mitochondrial membrane organization biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna 5'-end processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna 5'-end processing biological process from the curated GO Biological Process Annotations dataset.

mitochondrial asparaginyl-trna aminoacylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial asparaginyl-trna aminoacylation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial dna repair Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial dna repair biological process from the curated GO Biological Process Annotations dataset.

mitochondrial ribosome assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial ribosome assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial proton-transporting atp synthase complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial proton-transporting atp synthase complex assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna wobble uridine modification Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna wobble uridine modification biological process from the curated GO Biological Process Annotations dataset.

mitochondrial translation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial translation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial atp synthesis coupled electron transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iii assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iii assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial protein processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial protein processing biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial translation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial translation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial dna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial dna metabolic process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial calcium ion concentration Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial calcium ion concentration biological process from the curated GO Biological Process Annotations dataset.

trna aminoacylation for mitochondrial protein translation Gene Set

From GO Biological Process Annotations

genes participating in the trna aminoacylation for mitochondrial protein translation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial ornithine transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial ornithine transport biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

mitochondrial transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial tyrosyl-trna aminoacylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial tyrosyl-trna aminoacylation biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

mitochondrial electron transport, cytochrome c to oxygen Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial electron transport, cytochrome c to oxygen biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iii biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iii biogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

mitochondrial atp synthesis coupled proton transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial atp synthesis coupled proton transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

transcription from mitochondrial promoter Gene Set

From GO Biological Process Annotations

genes participating in the transcription from mitochondrial promoter biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna processing biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex i biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex i biogenesis biological process from the curated GO Biological Process Annotations dataset.

mitochondrial dna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial dna metabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial envelope Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial envelope cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex iv Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex iv cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex, catalytic core f(1) cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial alpha-ketoglutarate dehydrogenase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial alpha-ketoglutarate dehydrogenase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex i Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex i cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane peptidase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial endopeptidase clp complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial endopeptidase clp complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial fatty acid beta-oxidation multienzyme complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial fatty acid beta-oxidation multienzyme complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex ii Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex ii cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial small ribosomal subunit Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial small ribosomal subunit cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial part Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial part cellular component from the curated GO Cellular Component Annotations dataset.

sperm mitochondrial sheath Gene Set

From GO Cellular Component Annotations

proteins localized to the sperm mitochondrial sheath cellular component from the curated GO Cellular Component Annotations dataset.

integral component of mitochondrial membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of mitochondrial membrane cellular component from the curated GO Cellular Component Annotations dataset.

integral component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial large ribosomal subunit Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial large ribosomal subunit cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex, coupling factor f(o) cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial membrane part Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial membrane part cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial ribonuclease p complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial ribonuclease p complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial nucleoid Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial nucleoid cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial ribosome Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial ribosome cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial outer membrane translocase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial outer membrane translocase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial crista Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial crista cellular component from the curated GO Cellular Component Annotations dataset.

integral component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of mitochondrial membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of mitochondrial membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane presequence translocase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial inner membrane presequence translocase complex cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial chromosome Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial chromosome cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial permeability transition pore complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial permeability transition pore complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial degradosome Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial degradosome cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial intermembrane space protein transporter complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial intermembrane space Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial intermembrane space cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex iii Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex iii cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial pyruvate dehydrogenase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial pyruvate dehydrogenase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase, catalytic core Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase, catalytic core cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial tricarboxylic acid cycle enzyme complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial tricarboxylic acid cycle enzyme complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial matrix Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial matrix cellular component from the curated GO Cellular Component Annotations dataset.

cytoplasmic side of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the cytoplasmic side of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial heavy strand promoter anti-sense binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial heavy strand promoter anti-sense binding molecular function from the curated GO Molecular Function Annotations dataset.

mitochondrial light strand promoter anti-sense binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial light strand promoter anti-sense binding molecular function from the curated GO Molecular Function Annotations dataset.

mitochondrial light strand promoter sense binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial light strand promoter sense binding molecular function from the curated GO Molecular Function Annotations dataset.

mitochondrial ribosome binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial ribosome binding molecular function from the curated GO Molecular Function Annotations dataset.

mitochondrial heavy strand promoter sense binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial heavy strand promoter sense binding molecular function from the curated GO Molecular Function Annotations dataset.

multiple mitochondrial dna deletions Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the multiple mitochondrial dna deletions phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

muscle abnormality related to mitochondrial dysfunction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

depletion of mitochondrial dna in muscle tissue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the depletion of mitochondrial dna in muscle tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

mitochondrial myopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial complex ii Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex ii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial complex iv Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex iv phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial malic enzyme reduced Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial malic enzyme reduced phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscle abnormality related to mitochondrial dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased mitochondrial complex iii activity in liver tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased mitochondrial complex iii activity in liver tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial respiratory chain defects Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial respiratory chain defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of mitochondrial metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of mitochondrial metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial inheritance Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial respiratory chain Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial complex iii Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex iii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial atp synthase complex Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial atp synthase complex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

depletion of mitochondrial dna in liver Gene Set

From HPO Gene-Disease Associations

genes associated with the depletion of mitochondrial dna in liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial complex i Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex i phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial encephalopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple mitochondrial dna deletions Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple mitochondrial dna deletions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

depletion of mitochondrial dna in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the depletion of mitochondrial dna in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Mitochondrial Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mitochondrial Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Mitochondrial Myopathies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mitochondrial Myopathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Mitochondrial Encephalomyopathies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mitochondrial Encephalomyopathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

mitochondrial L-carnitine shuttle Gene Set

From HumanCyc Pathways

proteins participating in the mitochondrial L-carnitine shuttle pathway from the HumanCyc Pathways dataset.

dTMP de novo biosynthesis (mitochondrial) Gene Set

From HumanCyc Pathways

proteins participating in the dTMP de novo biosynthesis (mitochondrial) pathway from the HumanCyc Pathways dataset.

Mitochondrial import inner membrane translocase subunit Tim21 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim21 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aconitase, mitochondrial-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase, mitochondrial-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial chaperone BCS1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial chaperone BCS1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ATP synthase subunit g, animal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ATP synthase subunit g, animal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim44 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim44 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane transport complex, Sam37/metaxin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane transport complex, Sam37/metaxin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial carrier protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial carrier protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L27/L41, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L27/L41, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial degradasome RNA helicase subunit, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial degradasome RNA helicase subunit, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial genome maintenance exonuclease 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial genome maintenance exonuclease 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial brown fat uncoupling protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial brown fat uncoupling protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial 28S ribosomal protein S31 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial 28S ribosomal protein S31 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S24/S35, mitochondrial, conserved domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S24/S35, mitochondrial, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S27, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S27, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim10/Tim12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim10/Tim12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial carrier domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial carrier domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S23/Rsm25, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S23/Rsm25, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Small GTPase superfamily, mitochondrial Rho Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Small GTPase superfamily, mitochondrial Rho protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial fission regulator 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial fission regulator 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH dehydrogenase ubiquinone Fe-S protein 4, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH dehydrogenase ubiquinone Fe-S protein 4, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase complex, subunit Tim23 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase complex, subunit Tim23 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fatty acid oxidation complex, alpha subunit, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fatty acid oxidation complex, alpha subunit, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L55, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L55, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial substrate/solute carrier Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial substrate/solute carrier protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phenylalanyl-tRNA synthetase, class IIc, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phenylalanyl-tRNA synthetase, class IIc, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane translocase complex, subunit Tom20 domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane translocase complex, subunit Tom20 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein 63, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein 63, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S32, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S32, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit 8, mitochondrial, Metazoan Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit 8, mitochondrial, Metazoan protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial Rho-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial Rho-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane protease subunit 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane protease subunit 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L35, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L35, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane transport complex protein, metaxin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane transport complex protein, metaxin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane protein Mitofilin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane protein Mitofilin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S28, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S28, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit F6, mitochondrial subgroup Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit F6, mitochondrial subgroup protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L53, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L53, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim16 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial Na(+)/H(+) exchanger NHA2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial Na(+)/H(+) exchanger NHA2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adenylate kinase 4, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenylate kinase 4, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial F1-F0 ATP synthase subunit F, predicted Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial F1-F0 ATP synthase subunit F, predicted protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L1, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L1, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP synthase subunit s, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP synthase subunit s, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

T-cell activation inhibitor, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the T-cell activation inhibitor, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial glycoprotein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial glycoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial apoptosis-inducing factor, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial apoptosis-inducing factor, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit E, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit E, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial pyruvate carrier Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial pyruvate carrier protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit G, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit G, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hydroxymethylglutaryl-CoA lyase, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxymethylglutaryl-CoA lyase, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S23/S29, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S23/S29, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim50 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim50 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S29, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S29, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L51, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L51, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ribonuclease P, tRNA methyltransferase protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ribonuclease P, tRNA methyltransferase protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L28/L40, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L28/L40, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial proteolipid Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial proteolipid protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import protein TIM15 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import protein TIM15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import receptor subunit TOM7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import receptor subunit TOM7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S23/S25, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S23/S25, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L47, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L47, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial transcription factor TFB2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial transcription factor TFB2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F1 complex, epsilon subunit, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F1 complex, epsilon subunit, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Spermatogenesis-associated protein 19, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Spermatogenesis-associated protein 19, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adenylate kinase 3/4, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenylate kinase 3/4, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial matrix Mmp37 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial matrix Mmp37 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NAD(P) transhydrogenase, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NAD(P) transhydrogenase, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import receptor subunit TOM6 homologue Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import receptor subunit TOM6 homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase complex, subunit Tim17 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase complex, subunit Tim17 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S27/S33, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S27/S33, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ubiquitin ligase activator of NFKB 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ubiquitin ligase activator of NFKB 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial 18kDa protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial 18kDa protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Succinate dehydrogenase assembly factor 2, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Succinate dehydrogenase assembly factor 2, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit F6, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit F6, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lon protease homolog, chloroplastic/mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lon protease homolog, chloroplastic/mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial antiviral-signalling protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial antiviral-signalling protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import receptor subunit TOM5 homologue Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import receptor subunit TOM5 homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcium-binding mitochondrial carrier protein Aralar2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcium-binding mitochondrial carrier protein Aralar2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutamate-tRNA ligase, bacterial/mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutamate-tRNA ligase, bacterial/mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aspartate-tRNA ligase, class IIb, bacterial/mitochondrial-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aspartate-tRNA ligase, class IIb, bacterial/mitochondrial-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome c oxidase subunit VIIa-related, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome c oxidase subunit VIIa-related, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane translocase complex, subunit Tom22 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane translocase complex, subunit Tom22 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial Rho GTPase 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial Rho GTPase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial distribution/morphology family 35/apoptosis Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial distribution/morphology family 35/apoptosis protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S22, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S22, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L37, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L37, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ribosomal protein L48 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ribosomal protein L48 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit D, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit D, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

mitochondrial part Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial part cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

mitochondrial outer membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial outer membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

mitochondrial inner membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial inner membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

mitochondrial membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

decreased mitochondrial dna content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mitochondrial dna content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent sperm mitochondrial sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent sperm mitochondrial sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized mitochondrial cristae Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized mitochondrial cristae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mitochondrial proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mitochondrial proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mitochondrial proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mitochondrial proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

?mitochondrial complex (atp synthase) deficiency, nuclear type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex (atp synthase) deficiency, nuclear type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 4a (alpers type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 4a (alpers type) phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iv deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iv deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 6 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 6 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

complex i, mitochondrial respiratory chain, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the complex i, mitochondrial respiratory chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 12 (cardiomyopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 12 (cardiomyopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple mitochondrial dysfunctions syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple mitochondrial dysfunctions syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple mitochondrial dysfunctions syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex v (atp synthase) deficiency, nuclear type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex v (atp synthase) deficiency, nuclear type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial pyruvate carrier deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial pyruvate carrier deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{deafness, mitochondrial, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {deafness, mitochondrial, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial respiratory chain complex ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial respiratory chain complex ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 2 (myopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 2 (myopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 4b (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 4b (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial phosphate carrier deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial phosphate carrier deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 13 (encephalomyopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 13 (encephalomyopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial myopathy and sideroblastic anemia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial myopathy and sideroblastic anemia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial cox4 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial cox4 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iv deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iv deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 1 (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 1 (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial recessive ataxia syndrome (includes sando and scae) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial recessive ataxia syndrome (includes sando and scae) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 3 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 3 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 7 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 7 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex v (atp synthase) deficiency, nuclear type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex v (atp synthase) deficiency, nuclear type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 8b (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 8b (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

pepck deficiency, mitochondrial Gene Set

From OMIM Gene-Disease Associations

genes associated with the pepck deficiency, mitochondrial phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex 1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex 1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple mitochondrial dysfunctions syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term mitochondrial in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Mitochondrial biogenesis Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial biogenesis pathway from the Reactome Pathways dataset.

Import of palmitoyl-CoA into the mitochondrial matrix Gene Set

From Reactome Pathways

proteins participating in the Import of palmitoyl-CoA into the mitochondrial matrix pathway from the Reactome Pathways dataset.

Transcription from mitochondrial promoters Gene Set

From Reactome Pathways

proteins participating in the Transcription from mitochondrial promoters pathway from the Reactome Pathways dataset.

Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization Gene Set

From Reactome Pathways

proteins participating in the Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization pathway from the Reactome Pathways dataset.

Mitochondrial Fatty Acid Beta-Oxidation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial Fatty Acid Beta-Oxidation pathway from the Reactome Pathways dataset.

RNA Polymerase I, RNA Polymerase III, and Mitochondrial Transcription Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase I, RNA Polymerase III, and Mitochondrial Transcription pathway from the Reactome Pathways dataset.

Mitochondrial Uncoupling Proteins Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial Uncoupling Proteins pathway from the Reactome Pathways dataset.

Mitochondrial transcription initiation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial transcription initiation pathway from the Reactome Pathways dataset.

Mitochondrial ABC transporters Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial ABC transporters pathway from the Reactome Pathways dataset.

mitochondrial fatty acid beta-oxidation of unsaturated fatty acids Gene Set

From Reactome Pathways

proteins participating in the mitochondrial fatty acid beta-oxidation of unsaturated fatty acids pathway from the Reactome Pathways dataset.

Mitochondrial translation initiation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial translation initiation pathway from the Reactome Pathways dataset.

Mitochondrial tRNA aminoacylation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial tRNA aminoacylation pathway from the Reactome Pathways dataset.

Transcriptional activation of mitochondrial biogenesis Gene Set

From Reactome Pathways

proteins participating in the Transcriptional activation of mitochondrial biogenesis pathway from the Reactome Pathways dataset.

Mitochondrial transcription termination Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial transcription termination pathway from the Reactome Pathways dataset.

Mitochondrial translation termination Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial translation termination pathway from the Reactome Pathways dataset.

Mitochondrial protein import Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial protein import pathway from the Reactome Pathways dataset.

Mitochondrial translation elongation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial translation elongation pathway from the Reactome Pathways dataset.

Mitochondrial translation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial translation pathway from the Reactome Pathways dataset.

mitochondrial fatty acid beta-oxidation of saturated fatty acids Gene Set

From Reactome Pathways

proteins participating in the mitochondrial fatty acid beta-oxidation of saturated fatty acids pathway from the Reactome Pathways dataset.

Mitochondrial iron-sulfur cluster biogenesis Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial iron-sulfur cluster biogenesis pathway from the Reactome Pathways dataset.

Mitochondrial Gene Expression(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Mitochondrial Gene Expression(Mus musculus) pathway from the Wikipathways Pathways dataset.

Mitochondrial LC-Fatty Acid Beta-Oxidation(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Mitochondrial LC-Fatty Acid Beta-Oxidation(Mus musculus) pathway from the Wikipathways Pathways dataset.

Mitochondrial LC-Fatty Acid Beta-Oxidation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Mitochondrial LC-Fatty Acid Beta-Oxidation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Mitochondrial Gene Expression(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Mitochondrial Gene Expression(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Thyroid hormone metabolism, abnormal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Reflex, Abnormal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Reflex, Abnormal from the curated CTD Gene-Disease Associations dataset.

Neutrophil Chemotactic Response, Abnormal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset.

Thyroid Hormone Metabolism, Abnormal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset.

abnormal retinal correspondence Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

abnormal splicing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormal splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ekg, abnormal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ekg, abnormal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ekg, abnormal; brugada syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormal urogenital development Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormal fibrin polymerization and thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormal fibrin polymerization and thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormal Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term abnormal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

abnormal cannabidiol Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

abnormal eye physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal renal physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal gallbladder morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal gallbladder morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal gallbladder physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal intraocular pressure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal eating behavior Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal eating behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal thrombosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal leukocyte count Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal iris pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal iris pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal bone structure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal serum iron Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal emotion/affect behavior Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal bleeding Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal atrioventricular conduction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hair quantity Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal nervous system electrophysiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal male reproductive system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal external genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal ekg Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal ekg phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal axial skeleton morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal immunoglobulin level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal monocyte count Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal monocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal neutrophil cell number Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal platelet count Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal aggressive, impulsive or violent behavior Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

acquired abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal glomerular filtration rate Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal eye morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal testosterone level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal testosterone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal joint morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal motor neuron morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal biliary tract morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal neuron morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal genital system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal appendicular skeleton morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal cortical bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal electrophysiology of sinoatrial node origin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal respiratory system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal number of teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal circulating creatinine level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal peripheral nervous system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal autonomic nervous system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal platelet function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal muscle tone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal muscle tone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal diaphysis morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal diaphysis morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal spermatogenesis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal spermatogenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hemoglobin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal hemoglobin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal glucose homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal renal morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal dermatoglyphics Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal gallbladder morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal gallbladder morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ossification of hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone structure Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal branching pattern of the aortic arch Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal motor nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal maternal serum screening Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal maternal serum screening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal rod and cone electroretinograms Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal albumin level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal albumin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal enchondral ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal enchondral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal number of vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet membrane protein expression Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal platelet membrane protein expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal mitochondria in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal male reproductive system physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal placental size Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal placental size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal central microtubular pair morphology of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet granules Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal platelet granules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal subcutaneous fat tissue distribution Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal electroretinogram Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal lung lobation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal lung lobation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal flash visual evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal peripheral nervous system synaptic transmission Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine phosphate concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal urine phosphate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal drinking behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal drinking behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal sperm motility Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal fear/anxiety-related behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal renal corticomedullary differentiation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal humeral ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal humeral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal delayed hypersensitivity skin test Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal upper motor neuron morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal protein n-linked glycosylation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal echocardiogram Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal echocardiogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal serum ferritin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal female reproductive system physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hypothalamus morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hypothalamus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal axial skeleton morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal axial skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal calcification of the carpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal calcification of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal testosterone level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal testosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal peripheral myelination Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal speech discrimination Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal speech discrimination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal genital system morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal genital system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal morphology of bones of the lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal morphology of bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal liver function tests during pregnancy Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cortical bone morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hypothalamus physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hypothalamus physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal trabecular bone morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal electrophysiology of sinoatrial node origin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal metacarpal morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal metacarpal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal t3/t4 ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal t3/t4 ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal glycosylation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal iris vasculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal iris vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pupillary function Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pupillary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal posturing Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal posturing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal natural killer cell physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal external genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal immunoglobulin level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal immunoglobulin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal autonomic nervous system physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal monocyte count Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal monocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal atrial arrangement Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal atrial arrangement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal morphology of ulna Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal morphology of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal circulating renin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal circulating renin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal retinal folds Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal retinal folds phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pancreas size Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pancreas size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine sodium concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal urine sodium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vestibulo-ocular reflex Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vestibulo-ocular reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral pedicle morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral pedicle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal tendon morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal tendon morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal glucose homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal glucose homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal leukocyte count Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal leukocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal tarsal ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal spermatogenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal spermatogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal size of pituitary gland Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal size of pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine potassium concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal urine potassium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal synaptic transmission at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal synaptic transmission at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal peripheral nervous system morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pupillary light reflex Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pupillary light reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pyramidal signs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pyramidal signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal biliary tract morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal biliary tract morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pigmentation of the oral mucosa Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal number of incisors Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal localization of kidney Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal localization of kidney phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal elasticity of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal elasticity of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet volume Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vas deferens morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vas deferens morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal muscle tone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal muscle tone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal lower motor neuron morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ciliary motility Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ciliary motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal atrioventricular conduction Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal metatarsal ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal metatarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal st segment Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal sweat homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal sweat homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal nasal base Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pelvis bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal sperm morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal sperm morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ossification of the pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal isoelectric focusing of serum transferrin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal isoelectric focusing of serum transferrin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hemoglobin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hemoglobin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal morphology of bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal nasal morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal nasal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ossification involving the femoral head and neck Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal concentration of calcium in blood Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal emotion/affect behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal emotion/affect behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal epiphyseal ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine cytology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal urine cytology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal palmar dermatoglyphics Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal palmar dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal neuron morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal csf lactate level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal csf lactate level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal joint morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal joint morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral segmentation and fusion Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal internal genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal oral glucose tolerance Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal oral glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone collagen fibril morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal delivery Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal delivery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal middle ear reflexes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal middle ear reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cervical curvature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cervical curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bleeding Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal myelination Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal auditory evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal location of ears Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal location of ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cns myelination Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cns myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal eye physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal renal physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal synaptic transmission Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal eating behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal eating behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal atrioventricular connection Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal atrioventricular connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ventriculo-arterial connection Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ventriculo-arterial connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal anterior horn cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal germ cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal upper to lower segment ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal form of the vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal biliary tract physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine output Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal urine output phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal blistering of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal blistering of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal diaphysis morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal diaphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cholesterol homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cholesterol homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine citrate concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal urine citrate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal size of the palpebral fissures Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal size of the palpebral fissures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hand morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hand morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair quantity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair quantity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal anatomic location of the heart Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal anatomic location of the heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal iron deposition in mitochondria Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal iron deposition in mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal morphology of forearm bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal morphology of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal circulating aldosterone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal circulating aldosterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal male germ cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal platelet morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal circulating creatinine level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal circulating creatinine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet function Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal platelet function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal large intestine physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal facial expression Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine chloride concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal urine chloride concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vascular physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vascular physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal renal morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal renal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal heart morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal heart morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair laboratory examination Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal retinal pigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal lymphocyte count Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal lymphocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal conjugate eye movement Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal conjugate eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal autonomic nervous system morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal autonomic nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pulmonary lymphatics Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pulmonary lymphatics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pattern of respiration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal protein glycosylation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal protein glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair whorl Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair whorl phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal connection of the cardiac segments Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal connection of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cartilage collagen Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cartilage collagen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal umbilical stump bleeding Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal umbilical stump bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal social behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal social behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cortical gyration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cortical gyration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal serum iron Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal serum iron phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal number of permanent teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal sex determination Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal sex determination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal prolactin level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal prolactin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory system morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal respiratory system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal number of teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory epithelium morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal respiratory epithelium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal axonemal organization of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal axonemal organization of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal foot bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal neutrophil cell number Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal neutrophil cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet count Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal platelet count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal eye morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal eye morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cone-mediated electroretinogram Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cone-mediated electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal basal ganglia mri signal intensity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory motile cilium morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal respiratory motile cilium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal sensory nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal muscle glycogen content Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal appendicular skeleton morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal appendicular skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hand bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal number of erythroid precursors Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory motile cilium physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes