full name
myelin protein zero
synonyms
CHM, CMT1, CMT1B, CMT2I, CMT2J, CMT4E, CMTDI3, CMTDID, DSS, HMSNIB, MPP, P0, MPZ, ENSG00000158887
HGNC
HGNC:7225
Entrez Gene
Gene:4359
ENSEMBL
ENSG00000158887
location
chr: 1
start: 161274525
stop: 161279762
strand: -
OMIM
OMIM:159440:
MPZ
(Autosomal dominant inheritance)
OMIM:607791:
Charcot-Marie-Tooth disease, dominant intermediate D
OMIM:118200:
Charcot-Marie-Tooth disease, type 1B
OMIM:607677:
Charcot-Marie-Tooth disease, type 2I
OMIM:607736:
Charcot-Marie-Tooth disease, type 2J
OMIM:145900:
Dejerine-Sottas disease
OMIM:618184:
Hypomyelinating neuropathy, congenital, 2
OMIM:180800:
Roussy-Levy syndrome
transcripts
NM_000530.6
pathways
Cell adhesion molecules (CAMs)
[NCBI:83069]
[KEGG:hsa04514]
[PUBMED:15923648]
[PUBMED:12500939]
[PUBMED:15056568]
[PUBMED:14519386]
[PUBMED:12234363]
[PUBMED:10964748]
[PUBMED:15071551]
[PUBMED:15551862]
[PUBMED:14690046]
[PUBMED:9150551]
[PUBMED:14519398]
[PUBMED:14556710]
[PUBMED:11860281]
[PUBMED:10664064]
[PUBMED:9597126]
[PUBMED:11050419]
[PUBMED:12367625]
[PUBMED:10798271]
[PUBMED:16034094]
[PUBMED:15115723]
[PUBMED:15728677]
[PUBMED:11910893]
[PUBMED:15561584]
[PUBMED:15882774]
[PUBMED:12810109]
