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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:abnormal mitochondrial morphology
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Accession:MP:0006035 term browser browse the term
Definition:any structural anomaly of the semiautonomous, self replicating organelles that occur in varying numbers, shapes, and sizes in the cytoplasm of virtually all eukaryotic cells; mitochondria are notably the site of tissue respiration
Synonyms:exact_synonym: abnormal mitochondria morphology;   abnormal mitochondrion morphology



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abnormal mitochondrial crista morphology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Myc MYC proto-oncogene, bHLH transcription factor IMP RGD PMID:22629444 RGD:7240532 NCBI chr 7:93,593,705...93,598,633
Ensembl chr 7:93,593,705...93,598,630
JBrowse link
decreased mitochondrial DNA content term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ercc6 ERCC excision repair 6, chromatin remodeling factor IMP RGD PMID:31644904 RGD:126925983 NCBI chr16:7,764,983...7,835,587
Ensembl chr16:7,765,013...7,835,587
JBrowse link
G Ercc6em1Cgen ERCC excision repair 6, chromatin remodeling factor; CRISPR/Cas9 induced mutant 1, Cgen IMP RGD PMID:31644904 RGD:126925983
decreased mitochondrial size term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Myc MYC proto-oncogene, bHLH transcription factor IMP RGD PMID:22629444 RGD:7240532 NCBI chr 7:93,593,705...93,598,633
Ensembl chr 7:93,593,705...93,598,630
JBrowse link
increased mitochondrial size term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Fxn frataxin IMP RGD PMID:29223733 RGD:401793739 NCBI chr 1:221,874,007...221,897,543
Ensembl chr 1:221,872,420...221,897,540
JBrowse link

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  mammalian phenotype 5407
    cellular phenotype 192
      abnormal cell morphology 47
        abnormal intracellular organelle morphology 23
          abnormal mitochondrial morphology 5
            abnormal fat cell mitochondrial morphology + 0
            abnormal fetal cardiomyocyte mitochondrial morphology 0
            abnormal hepatocyte mitochondrial morphology + 0
            abnormal mitochondrial chromosome morphology + 3
            abnormal mitochondrial inner membrane morphology + 1
            abnormal mitochondrial matrix morphology 0
            abnormal mitochondrial shape 0
            abnormal muscle fiber mitochondrial morphology + 0
            abnormal neuron mitochondrial morphology + 0
            abnormal sperm mitochondrial morphology + 0
            decreased mitochondrial number 0
            decreased mitochondrial size + 1
            increased mitochondrial number 0
            increased mitochondrial size + 1
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