Human (GRCh38.p14)
Description

R3H domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28270]

Gene Synonyms

C19ORF22, MGC16353

Location

Chromosome 19: 896,503-913,245 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 8 transcripts (splice variants) and 181 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000361574.10R3HDM4-2011803268aaENSP00000355385.4
 
Protein coding
CCDS12048Q96D70 NM_138774.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000587975.2R3HDM4-2031765247aaENSP00000464744.1
 
Protein coding
K7EIG9 -GENCODE basicTSL:3
ENST00000626716.1R3HDM4-20813845aaENSP00000486092.1
 
Protein coding
K7ER32 -GENCODE basicTSL:5
ENST00000589428.5R3HDM4-204170497aaENSP00000466823.1
 
Nonsense mediated decay
K7EN78 -TSL:3
ENST00000590454.2R3HDM4-206100645aaENSP00000468026.1
 
Nonsense mediated decay
K7ER32 -TSL:3
ENST00000591829.5R3HDM4-207823No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000589445.1R3HDM4-205705No protein-
 
Retained intron
--TSL:3
ENST00000586080.1R3HDM4-202537No protein-
 
Retained intron
--TSL:4