Human (GRCh38.p14)
Description

PR/SET domain 5 [Source:HGNC Symbol;Acc:HGNC:9349]

Gene Synonyms

PFM2

Location

Chromosome 4: 120,684,919-120,922,870 reverse strand.

GRCh38:CM000666.2

About this gene

This gene has 12 transcripts (splice variants), 203 orthologues, 4 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000264808.8PRDM5-2015207630aaENSP00000264808.3
 
Protein coding
CCDS3716Q9NQX1-1 NM_018699.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000394435.2PRDM5-2022492111aaENSP00000377955.2
 
Protein coding
Q9NQX1-3 -GENCODE basicTSL:1
ENST00000428209.6PRDM5-2032338599aaENSP00000404832.2
 
Protein coding
CCDS75188Q9NQX1-2 -GENCODE basicTSL:1
ENST00000515109.5PRDM5-2122259501aaENSP00000422309.1
 
Protein coding
CCDS75187Q9NQX1-4 -GENCODE basicTSL:1
ENST00000502409.1PRDM5-2041044145aaENSP00000424861.1
 
Nonsense mediated decay
H0Y9S1 -TSL:5CDS 5' incomplete
ENST00000506065.1PRDM5-208696No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000505033.1PRDM5-206576No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000513741.1PRDM5-211210No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000505484.5PRDM5-2072396No protein-
 
Retained intron
--TSL:1
ENST00000512845.5PRDM5-2101249No protein-
 
Retained intron
--TSL:1
ENST00000503661.5PRDM5-205847No protein-
 
Retained intron
--TSL:3
ENST00000507611.1PRDM5-209535No protein-
 
Retained intron
--TSL:2