The MPV17 gene homepage

General information
Gene symbol MPV17
Gene name MpV17 mitochondrial inner membrane protein
Chromosome 2
Chromosomal band p23.3
Imprinted Unknown
Genomic reference NG_008075.1
Transcript reference NM_002437.4
Exon/intron information NM_002437.4 exon/intron table
Associated with diseases CMT2EE, MTDPS6
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 42
Unique public DNA variants reported 29
Individuals with public variants 28
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated February 26, 2024
Version MPV17:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_002437.4.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/MPV17
HGNC 7224
Entrez Gene 4358
PubMed articles MPV17
OMIM - Gene 137960
OMIM - Diseases CMT2EE (Charcot-Marie-Tooth disease, axonal, type 2EE)
MTDPS6 (mitochondrial DNA depletion syndrome (hepatocerebral), type 6 (MTDPS-6))
HGMD MPV17
GeneCards MPV17
GeneTests MPV17
Orphanet MPV17


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00013812 2 MpV17 mitochondrial inner membrane protein NM_002437.4 NP_002428.1 42


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