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Human (GRCh38.p14)
Description

PR/SET domain 6 [Source:HGNC Symbol;Acc:HGNC:9350]

Gene Synonyms

KMT8C, PRISM

Location

Chromosome 5: 123,089,241-123,194,266 forward strand.

GRCh38:CM000667.2

About this gene

This gene has 5 transcripts (splice variants), 190 orthologues, 36 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000407847.5PRDM6-2019147595aaENSP00000384725.3
 
Protein coding
CCDS47259Q9NQX0-3 NM_001136239.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00000890813.1PRDM6-2052920595aaENSP00000560872.1
 
Protein coding
CCDS47259--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000434521.1PRDM6-20369973aaENSP00000390919.1
 
Nonsense mediated decay
H7BZR2 -TSL:2CDS 5' incomplete
ENST00000464424.1PRDM6-204514No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000427739.1PRDM6-202256No protein-
 
Protein coding CDS not defined
--TSL:3