Human (GRCh38.p14)
Description

exosome component 9 [Source:HGNC Symbol;Acc:HGNC:9137]

Gene Synonyms

P5, P6, PM/SCL-75, PMSCL1, RRP45, RRP45P

Location

Chromosome 4: 121,801,318-121,817,021 forward strand.

GRCh38:CM000666.2

About this gene

This gene has 12 transcripts (splice variants), 210 orthologues, 2 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000243498.10EXOSC9-2011587439aaENSP00000243498.5
 
Protein coding
CCDS3722Q06265-1 NM_005033.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000512454.5EXOSC9-2111543423aaENSP00000425782.1
 
Protein coding
D6RIY6 -GENCODE basicTSL:1
ENST00000379663.7EXOSC9-2021529456aaENSP00000368984.3
 
Protein coding
CCDS34057Q06265-2 -GENCODE basicTSL:1
ENST00000509800.5EXOSC9-207757226aaENSP00000422205.1
 
Protein coding
D6R905 -TSL:3CDS 3' incomplete
ENST00000511132.1EXOSC9-209515172aaENSP00000424504.1
 
Protein coding
H0Y9L5 -TSL:5CDS 5' and 3' incomplete
ENST00000513654.5EXOSC9-2123882242aaENSP00000423476.1
 
Nonsense mediated decay
D6RA17 -TSL:2
ENST00000511454.5EXOSC9-21073386aaENSP00000421845.1
 
Nonsense mediated decay
D6RAP4 -TSL:5
ENST00000509980.5EXOSC9-2081317No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000503139.5EXOSC9-2031204No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000503236.1EXOSC9-204644No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000508212.5EXOSC9-206612No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000506201.1EXOSC9-205590No protein-
 
Retained intron
--TSL:2