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Search results 401
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Trmt10c
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0.016s
Type
Details
Score
Publication
First Author:
Mouse Genome Informatics Scientific Curators
Year:
2009
Journal:
Database Download
Title:
Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
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Publication
First Author:
Bairoch A
Year:
1999
Journal:
Database Release
Title:
SWISS-PROT Annotated protein sequence database
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Publication
First Author:
Mouse Genome Informatics Scientific Curators
Year:
2005
Title:
Obtaining and loading genome assembly coordinates from NCBI annotations
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Publication
First Author:
Mouse Genome Database and National Center for Biotechnology Information
Year:
2000
Journal:
Database Release
Title:
Entrez Gene Load
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Publication
First Author:
Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year:
2010
Journal:
Database Download
Title:
Consensus CDS project
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Publication
First Author:
Mouse Genome Informatics
Year:
2010
Journal:
Database Release
Title:
Protein Ontology Association Load.
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Publication
First Author:
Allen Institute for Brain Science
Year:
2004
Journal:
Allen Institute
Title:
Allen Brain Atlas: mouse riboprobes
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Publication
First Author:
Mouse Genome Informatics Scientific Curators
Year:
2005
Title:
Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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Publication
First Author:
Metodiev MD
Year:
2016
Journal:
Am J Hum Genet
Title:
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies.
Volume:
98
Issue:
5
Pages:
993-1000
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DO Term
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Protein Domain
Type:
Family
Description:
Mitochondrial RNase P (mtRNase P) cleaves tRNA molecules in their 5'-ends and consists of 3 components: a tRNA methyltransferase (MRPP1/TRMT10), a dehydrogenase/reductase-family member (MRPP2/HSD17B10), and MRPP3 (KIAA03910) [].This entry represents tRNA methyltransferase 10 homologue C (TRMT10C), which is a metazoa homologue to yeast TRM10, a tRNA m1G methyltransferase responsible for modification at position 9. In humans there are three TRM10 orthologues. Mutations in TRMT10C cause mitochondrial disease [].
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Publication
First Author:
Holzmann J
Year:
2008
Journal:
Cell
Title:
RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme.
Volume:
135
Issue:
3
Pages:
462-74
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Protein
Organism:
Mus musculus/domesticus
Length:
414
Fragment?:
false
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