Human (GRCh38.p14)
Description

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

Gene Synonyms

CMT1, CMT1B, CMT2I, CMT2J, HMSNIB, P0

Location

Chromosome 1: 161,304,735-161,309,968 reverse strand.

GRCh38:CM000663.2

About this gene

This gene has 9 transcripts (splice variants), 174 orthologues, 6 paralogues and is associated with 16 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000533357.5MPZ-2061951248aaENSP00000432943.1
 
Protein coding
CCDS1229P25189-1 NM_000530.8MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000672602.2MPZ-2081951312aaENSP00000500814.2
 
Protein coding
CCDS91087A0A5F9ZI26 -GENCODE basic
ENST00000491222.5MPZ-204182452aaENSP00000431441.1
 
Protein coding
E9PL80 -GENCODE basicTSL:2
ENST00000672287.2MPZ-207182452aaENSP00000499818.2
 
Protein coding
E9PL80 -GENCODE basic
ENST00000526189.3MPZ-2051276221aaENSP00000488104.2
 
Protein coding
A0A0J9YWT2 -GENCODE basicTSL:3
ENST00000463290.5MPZ-2011693248aaENSP00000431538.1
 
Nonsense mediated decay
CCDS1229P25189-1 -TSL:1
ENST00000674861.1MPZ-2091951No protein-
 
Retained intron
---
ENST00000476410.1MPZ-202878No protein-
 
Retained intron
--TSL:3
ENST00000488271.1MPZ-203366No protein-
 
Retained intron
--TSL:2