Annotation inferences using phylogenetic trees
Gene Ontology annotation through association of InterPro records with GO terms
Gene Ontology annotation based on curation of immunofluorescence data
Combined Automated Annotation using Multiple IEA Methods
Huntingtin interacting proteins are genetic modifiers of neurodegeneration.
A splicing mutation in the novel mitochondrial protein DNAJC11 causes motor neuron pathology associated with cristae disorganization, and lymphoid abnormalities in mice.
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The full-length 63 kDa DNAJC11 isoform localizes to the periphery of the mitochondrial outer membrane and is assembled into a high-molecular-weight complex; mitofilin/SAM50 downregulation reduces DNAJC11 levels.
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A hypomorphic DnaJC11 splicing mutation in mice causes motor neuron pathology with mitochondrial cristae disorganization and loss of proper inner-membrane organization.
QIL1 is a novel mitochondrial protein required for MICOS complex stability and cristae morphology.
Evolution and structural organization of the mitochondrial contact site (MICOS) complex and the mitochondrial intermembrane space bridging (MIB) complex.
A reference map of the human binary protein interactome.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Multimodal cell maps as a foundation for structural and functional genomics.
UniProt entry Q9NVH1 (DJC11_HUMAN), DnaJ homolog subfamily C member 11