Human (GRCh37.p13)
Description

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

Gene Synonyms

BCS2, PFM2

Location

Chromosome 4: 121,606,074-121,844,025 reverse strand.

GRCh37:CM000666.1

About this gene

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

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000264808.3PRDM5-0015330630aaENSP00000264808.3
 
Protein coding
CCDS3716Q9NQX1 NM_018699.2GENCODE basic
ENST00000394435.2PRDM5-0022492111aaENSP00000377955.2
 
Protein coding
Q9NQX1 -GENCODE basic
ENST00000428209.2PRDM5-0062338599aaENSP00000404832.2
 
Protein coding
Q9NQX1 -GENCODE basic
ENST00000515109.1PRDM5-0052259501aaENSP00000422309.1
 
Protein coding
Q0VAI9 -GENCODE basic
ENST00000502409.1PRDM5-0091044145aaENSP00000424861.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000506065.1PRDM5-011696No protein-
 
Processed transcript
---
ENST00000505033.1PRDM5-007576No protein-
 
Processed transcript
---
ENST00000513741.1PRDM5-012210No protein-
 
Processed transcript
---
ENST00000505484.1PRDM5-0042396No protein-
 
Retained intron
---
ENST00000512845.1PRDM5-0031249No protein-
 
Retained intron
---
ENST00000503661.1PRDM5-010847No protein-
 
Retained intron
---
ENST00000507611.1PRDM5-008535No protein-
 
Retained intron
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