Human (GRCh38.p14)
Description

peroxisomal biogenesis factor 16 [Source:HGNC Symbol;Acc:HGNC:8857]

Location

Chromosome 11: 45,909,663-45,918,812 reverse strand.

GRCh38:CM000673.2

About this gene

This gene has 11 transcripts (splice variants), 201 orthologues and is associated with 8 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000378750.10PEX16-2021668336aaENSP00000368024.5
 
Protein coding
CCDS31472Q9Y5Y5-1 NM_004813.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000532681.5PEX16-2101639241aaENSP00000434654.1
 
Protein coding
E9PP98 -GENCODE basicTSL:3
ENST00000241041.7PEX16-2011479346aaENSP00000241041.3
 
Protein coding
CCDS7917Q9Y5Y5-2 -GENCODE basicTSL:1
ENST00000525192.5PEX16-204903160aaENSP00000431309.1
 
Protein coding
E9PLS4 -TSL:5CDS 3' incomplete
ENST00000533151.5PEX16-211563183aaENSP00000433045.1
 
Protein coding
E9PMM3 -TSL:3CDS 3' incomplete
ENST00000528674.5PEX16-20779564aaENSP00000434060.1
 
Nonsense mediated decay
E9PSC6 -TSL:3
ENST00000529030.1PEX16-20879460aaENSP00000432486.1
 
Nonsense mediated decay
E9PQW0 -TSL:3
ENST00000525229.5PEX16-20558852aaENSP00000431132.1
 
Nonsense mediated decay
E9PMS3 -TSL:3
ENST00000532554.5PEX16-209546No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000523721.2PEX16-203325No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000527371.1PEX16-206362No protein-
 
Retained intron
--TSL:3