Gene table of MPZ : myelin protein zero

Gene-disease associations table

Disease IDDisease nameSource of annotation with MPZOMIM linkNumber of associated genesgenes
PS118220CHARCOT-MARIE-TOOTH DISEASEClinVar, OMIM, HUMSAVAR link to OMIM 48KARS, FIG4, PRPS1, FGD4, MPZ, KIF1B, NEFL, GJB1, VCP, GDAP1, AIFM1, IGHMBP2, SH3TC2, TRIM2, JPH1, PLEKHG5, NEFH, NAGLU, TRPV4, HARS, HSPB8, HSPB1, PMP22, MED25, SPG11, SBF1, DYNC1H1, SURF1, DNM2, NDRG1, MARS, SBF2, RAB7A, MORC2, AARS, COX6A1, PDK3, DHTKD1, HK1, LMNA, LRSAM1, EGR2, PRX, MTMR2, LITAF, MFN2, YARS, GARS
180800ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIAOMIM, HUMSAVAR link to OMIM 2PMP22, MPZ

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Annotation of the gene MPZ

Associated genes in ENSEMBL
Associated proteins - SwissProt Accession ID
Associated PDB IDs
Cytogenetic Band
Tandem repeats annotation
Transcription regulation as annotated in TRRUST

It is regulated by the following TF:

Associated KEGG pathways
KEGG pathwayKEGG IDKEGG IC
Cell adhesion molecules (CAMs)hsa045145.36
Associated REACTOME pathways
Associated GO terms for Molecular function
GO termGO IDGO IC
structural molecule activityGO:00051983.1