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Human (GRCh38.p14)
Description

peroxisomal membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:9716]

Gene Synonyms

MPV17L3, PMP22

Location

Chromosome 12: 132,687,571-132,708,576 forward strand.

GRCh38:CM000674.2

About this gene

This gene has 17 transcripts (splice variants), 168 orthologues and 3 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000317479.8PXMP2-201970195aaENSP00000321271.3
 
Protein coding
CCDS9279Q9NR77 NM_018663.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00001143363.1PXMP2-217986195aaENSP00000806756.1
 
Protein coding
CCDS9279--Ensembl Canonical ExtendedGENCODE BasicAPPRIS P1
ENST00000856532.2PXMP2-2061231239aaENSP00000526591.1
 
Protein coding
--GENCODE Basic
ENST00001116681.1PXMP2-2141221183aaENSP00000786486.1
 
Protein coding
--GENCODE Basic
ENST00000979357.1PXMP2-211117689aaENSP00000649174.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000856534.2PXMP2-2081068223aaENSP00000526593.1
 
Protein coding
--GENCODE Basic
ENST00001116680.1PXMP2-213956245aaENSP00000786485.1
 
Protein coding
--GENCODE Basic
ENST00000856533.2PXMP2-207905155aaENSP00000526592.1
 
Protein coding
--GENCODE Basic
ENST00000856535.2PXMP2-209837146aaENSP00000526594.1
 
Protein coding
--GENCODE Basic
ENST00001116679.1PXMP2-212769181aaENSP00000786484.1
 
Protein coding
--GENCODE Basic
ENST00000428960.3PXMP2-202762227aaENSP00000398708.3
 
Protein coding
F5GXM0 -TSL:3CDS 5' incomplete
ENST00000543589.6PXMP2-205703160aaENSP00000446049.1
 
Protein coding
F5H4N4 -GENCODE PrimaryGENCODE BasicTSL:3
ENST00001124003.1PXMP2-216671188aaENSP00000793808.1
 
Protein coding
--GENCODE Basic
ENST00000454379.2PXMP2-20353783aaENSP00000484702.1
 
Protein coding
A0A087X249 -TSL:3CDS 5' incomplete
ENST00000979355.1PXMP2-2101006147aaENSP00000649172.1
 
Nonsense mediated decay
---
ENST00001124002.1PXMP2-21599989aaENSP00000793807.1
 
Nonsense mediated decay
---
ENST00000539093.2PXMP2-20451649aaENSP00000444486.2
 
Nonsense mediated decay
F5GZF7 -TSL:3CDS 5' incomplete