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Human (GRCh37.p13)
Description

myelin protein zero [Source:HGNC Symbol;Acc:7225]

Gene Synonyms

CHM, CMT1, CMT1B, CMT2I, CMT2J, CMT4E, CMTDI3, CMTDID, DSS, HMSNIB, MPP, P0

Location

Chromosome 1: 161,274,525-161,279,762 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 8 transcripts (splice variants), 5 paralogues and is associated with 18 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000533357.1MPZ-0011955248aaENSP00000432943.1
 
Protein coding
CCDS1229E9PL80 P25189 NM_000530.6Ensembl CanonicalGENCODE basic
ENST00000360451.6MPZ-2021951258aaENSP00000353634.6
 
Protein coding
E9PL80 P25189 -GENCODE basic
ENST00000491222.2MPZ-005182452aaENSP00000431441.1
 
Protein coding
E9PL80 -GENCODE basic
ENST00000336559.4MPZ-201820250aaENSP00000337777.4
 
Protein coding
E7EWP3 Q14902 -GENCODE basic
ENST00000463290.1MPZ-0021693248aaENSP00000431538.1
 
Nonsense mediated decay
CCDS1229E9PL80 P25189 --
ENST00000526189.1MPZ-006957No protein-
 
Processed transcript
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ENST00000476410.1MPZ-003878No protein-
 
Retained intron
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ENST00000488271.1MPZ-004366No protein-
 
Retained intron
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