Protein MPV17 is a protein that in humans is encoded by the MPV17 gene. It is a mitochondrial inner membrane protein, which has a so far largely unknown...
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later in infancy or in childhood. In MDDS associated with mutations in MPV17 that primarily affect the brain and the liver, the symptoms are similar...
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(June 28, 2009). "Navajo Neurohepatopathy Is Caused by a Mutation in the MPV17 Gene". The American Journal of Human Genetics. 79 (3): 544–548. doi:10.1086/506913...
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MPV17 mitochondrial inner membrane protein like 2 is a protein that in humans is encoded by the MPV17L2 gene. GRCh38: Ensembl release 89: ENSG00000254858...
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HGNC:1180 Q15777 9759 MPRIP HGNC:30321 Q6WCQ1 9760 MPST HGNC:7223 P25325 9761 MPV17 HGNC:7224 P39210 9762 MPV17L HGNC:26827 Q2QL34 9763 MPV17L2 HGNC:28177 Q567V2...
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Autosomal dominant CMT2DD 618036 ATP1A1 1p13.1 Autosomal dominant CMT2EE 618400 MPV17 2p23.3 Autosomal recessive CMT3 CMT3 145900 MPZ EGR2 PMP22 PRX 1q23.3 10q21...
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C10orf2 Mitochondrial DNA depletion syndrome, hepatocerebral form; 251880; MPV17 Mitochondrial DNA depletion syndrome, myopathic form; 609560; TK2 Mitochondrial...
234 KB (18,877 words) - 15:43, 9 May 2024