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- CHCHD10 abstract "CHCHD10, whose full official name is coiled-coil-helix-coiled-coil-helix domain containing 10, is a gene found in Humans encoding a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. CHCHD10-related disorders include mitochondrial myopathy, amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), late-onset spinal motor neuronopathy (SMAJ), and cerebellar ataxia. Alternative splicing of this gene results in multiple transcript variants.".
- CHCHD10 wikiPageExternalLink CHCHD10.
- CHCHD10 wikiPageID "48518958".
- CHCHD10 wikiPageLength "1660".
- CHCHD10 wikiPageOutDegree "14".
- CHCHD10 wikiPageRevisionID "695695215".
- CHCHD10 wikiPageWikiLink Alternative_splicing.
- CHCHD10 wikiPageWikiLink Amyotrophic_lateral_sclerosis.
- CHCHD10 wikiPageWikiLink Category:Human_genes.
- CHCHD10 wikiPageWikiLink Category:RNA_splicing.
- CHCHD10 wikiPageWikiLink Cerebellar_ataxia.
- CHCHD10 wikiPageWikiLink Crista.
- CHCHD10 wikiPageWikiLink Frontotemporal_dementia.
- CHCHD10 wikiPageWikiLink Human.
- CHCHD10 wikiPageWikiLink Intermembrane_space.
- CHCHD10 wikiPageWikiLink Late-onset_spinal_motor_neuronopathy.
- CHCHD10 wikiPageWikiLink Mitochondrial_myopathy.
- CHCHD10 wikiPageWikiLink Mitochondrion.
- CHCHD10 wikiPageWikiLink Oxidative_phosphorylation.
- CHCHD10 wikiPageWikiLink Protein.
- CHCHD10 wikiPageWikiLinkText "CHCHD10".
- CHCHD10 wikiPageUsesTemplate Template:NLM_content.
- CHCHD10 wikiPageUsesTemplate Template:Neuroscience-stub.
- CHCHD10 wikiPageUsesTemplate Template:Reflist.
- CHCHD10 subject Category:Human_genes.
- CHCHD10 subject Category:RNA_splicing.
- CHCHD10 hypernym Domain.
- CHCHD10 type Protein.
- CHCHD10 comment "CHCHD10, whose full official name is coiled-coil-helix-coiled-coil-helix domain containing 10, is a gene found in Humans encoding a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. CHCHD10-related disorders include mitochondrial myopathy, amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), late-onset spinal motor neuronopathy (SMAJ), and cerebellar ataxia.".
- CHCHD10 label "CHCHD10".
- CHCHD10 sameAs Q18057616.
- CHCHD10 sameAs Q18057616.
- CHCHD10 wasDerivedFrom CHCHD10?oldid=695695215.
- CHCHD10 isPrimaryTopicOf CHCHD10.