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18 records found for search term Mrpl49
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1309920Mrpl49mitochondrial ribosomal protein L49ENCODES a protein that exhibits structural constituent of ribosome (inferred); INVOLVED IN translation (inferred); ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial large ribosomal subunit (ortholo1212775357212779364Rat94symbol , PhenoGengene, protein-coding, VALIDATED [RefSeq]
1320522MRPL49mitochondrial ribosomal protein L49Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryot116512218365127371Human103symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1320523Mrpl49mitochondrial ribosomal protein L49Predicted to be a structural constituent of ribosome. Predicted to be involved in mitochondrial translation. Located in mitochondrion. Is expressed in several structures, including central nervous system; early conceptus; gonad; liver; and retina. Orthologous to human MRPL491961036606107785Mouse107symbol , PhenoGen , descriptiongene, protein-coding, VALIDATED [RefSeq]
8968923Mrpl49mitochondrial ribosomal protein L49ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial large ribosomal subunit (ortholog); mitochondrial ribosome (ortholog); mitochondrion (ortholog)NW_0049554222007573920078278Chinchilla11symbolgene, protein-coding, MODEL [RefSeq]
11918550MRPL49mitochondrial ribosomal protein L49ENCODES a protein that exhibits structural constituent of ribosome (inferred); INVOLVED IN translation (inferred); ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial large ribosomal subunit (inferre116048464560489718Bonobo18symbolgene, protein-coding, MODEL [RefSeq]
12279467MRPL49mitochondrial ribosomal protein L49ENCODES a protein that exhibits structural constituent of ribosome (inferred); INVOLVED IN translation (inferred); ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial large ribosomal subunit (inferre185206857652072642Dog18symbolgene, protein-coding, MODEL [RefSeq]
12487726Mrpl49mitochondrial ribosomal protein L49ENCODES a protein that exhibits structural constituent of ribosome (inferred); INVOLVED IN translation (inferred); ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial large ribosomal subunit (inferreNW_00493659942433104246546Squirrel18symbolgene, protein-coding, MODEL [RefSeq]
18920713Mrpl49mitochondrial ribosomal protein L49ENCODES a protein that exhibits structural constituent of ribosome (inferred); INVOLVED IN translation (inferred); ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial large ribosomal subunit (inferreNaked Mole-Rat18symbolgene, protein-coding, MODEL [RefSeq]
14203191MRPL49mitochondrial ribosomal protein L49ENCODES a protein that exhibits metal ion binding (inferred); structural constituent of ribosome (inferred); INVOLVED IN translation (inferred); ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial laPig19symbolgene, protein-coding, VALIDATED [RefSeq]
14377586mRpL49Flysymbolgene, null
284026047mrpl49Tropical Clawed Frogsymbolgene, null
14380780MRPL49Yeastsymbolgene, null
18411959MRPL49mitochondrial ribosomal protein L49ENCODES a protein that exhibits structural constituent of ribosome (inferred); INVOLVED IN translation (inferred); ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial ribosome (ortholog)Green Monkey16symbolgene, protein-coding, MODEL [RefSeq]
626144527Mrpl49mitochondrial ribosomal protein L49ASSOCIATED WITH Combined Oxidative Phosphorylation Deficiency 60 (ortholog); melanoma (ortholog); Perrault Syndrome 1 (ortholog); FOUND IN mitochondrial large ribosomal subunit (ortholog); mitochondrial ribosome (ortholog); mitochondrion (ortholog)Black Rat11symbolgene, protein-coding, MODEL [RefSeq]
288057364mrpl49.LAfrican Clawed Frogsymbolgene, null
15567441Gm52998predicted gene, 52998Mouseold_gene_namegene, processed_pseudogene
4144461MRPL49P1mitochondrial ribosomal protein L49 pseudogene 156467485464675390Humansymbol , COSMIC , Human Proteome Mapgene, pseudo, INFERRED [RefSeq]
1342652MRPL49P2mitochondrial ribosomal protein L49 pseudogene 281637461916375086Humansymbol , COSMIC , Human Proteome Mapgene, pseudo, INFERRED [RefSeq]