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Human (GRCh38.p14)
Description

protein arginine methyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:25099]

Gene Synonyms

FLJ46629, PRMT10

Location

Chromosome 4: 147,635,654-147,684,163 reverse strand.

GRCh38:CM000666.2

About this gene

This gene has 11 transcripts (splice variants), 201 orthologues, 7 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000322396.7PRMT9-2013461845aaENSP00000314396.6
 
Protein coding
CCDS3771Q6P2P2-1 NM_138364.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000960614.1PRMT9-2105640861aaENSP00000630673.1
 
Protein coding
--GENCODE Basic
ENST00000865624.1PRMT9-2053202766aaENSP00000535683.1
 
Protein coding
--GENCODE Basic
ENST00000865625.1PRMT9-2063033710aaENSP00000535684.1
 
Protein coding
--GENCODE Basic
ENST00000960615.1PRMT9-2112755823aaENSP00000630674.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000865626.1PRMT9-2072645775aaENSP00000535685.1
 
Protein coding
--GENCODE Basic
ENST00000940715.1PRMT9-2092182626aaENSP00000610774.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000940714.1PRMT9-208854175aaENSP00000610773.1
 
Protein coding
--GENCODE Basic
ENST00000514886.1PRMT9-204267466aaENSP00000426732.1
 
Nonsense mediated decay
D6REN0 -TSL:2
ENST00000510269.5PRMT9-2022012No protein-
 
Retained intron
--TSL:2
ENST00000511687.1PRMT9-203401No protein-
 
Retained intron
--TSL:2