Human (GRCh37.p13)
Description

excision repair cross-complementing rodent repair deficiency, complementation group 4 [Source:HGNC Symbol;Acc:3436]

Gene Synonyms

ERCC11, FANCQ, RAD1, XPF

Location

Chromosome 16: 14,014,014-14,046,202 forward strand.

GRCh37:CM000678.1

About this gene

This gene has 8 transcripts (splice variants) and is associated with 68 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000311895.7ERCC4-0016758916aaENSP00000310520.7
 
Protein coding
CCDS32390B4DXD8 Q92889 NM_005236.2GENCODE basic
ENST00000575156.1ERCC4-0032073372aaENSP00000459933.1
 
Protein coding
A5PKV6 -GENCODE basic
ENST00000462862.1ERCC4-00272135aaENSP00000461322.1
 
Nonsense mediated decay
I3L4K0 -CDS 5' incomplete
ENST00000574194.1ERCC4-00758375aaENSP00000461883.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000574781.1ERCC4-006638No protein-
 
Processed transcript
---
ENST00000389138.3ERCC4-0042106No protein-
 
Retained intron
---
ENST00000576348.1ERCC4-005604No protein-
 
Retained intron
---
ENST00000573018.1ERCC4-008523No protein-
 
Retained intron
---