Human (GRCh38.p14)
Description

required for excision 1-B domain containing [Source:HGNC Symbol;Acc:HGNC:26098]

Gene Synonyms

C19ORF60, FLJ20850, FLJ30108, FLJ34606, FLJ37391

Location

Chromosome 19: 18,588,685-18,592,337 forward strand.

GRCh38:CM000681.2

About this gene

This gene has 8 transcripts (splice variants) and 80 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000358607.11REX1BD-201767201aaENSP00000351422.5
 
Protein coding
CCDS42524Q96EN9-1 NM_001100418.2MANE SelectEnsembl CanonicalGENCODE basicTSL:1
ENST00000450195.6REX1BD-202702179aaENSP00000398467.1
 
Protein coding
CCDS46019Q96EN9-3 -GENCODE basicAPPRIS P1TSL:1
ENST00000595490.1REX1BD-20441060aaENSP00000469859.1
 
Protein coding
M0QYI9 -TSL:3CDS 5' incomplete
ENST00000601736.1REX1BD-20849166aaENSP00000471429.1
 
Nonsense mediated decay
M0R0T3 -TSL:2
ENST00000595077.1REX1BD-2032465No protein-
 
Retained intron
--TSL:NA
ENST00000600997.5REX1BD-2072275No protein-
 
Retained intron
--TSL:2
ENST00000598375.5REX1BD-2061792No protein-
 
Retained intron
--TSL:5
ENST00000597371.1REX1BD-2051081No protein-
 
Retained intron
--TSL:3