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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 82 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ERCC4-001ENST00000311895.76758916aaENSP00000310520.7
 
Protein coding
CCDS32390B4DXD8 Q92889 NM_005236
NP_005227
GENCODE basic
ERCC4-003ENST00000575156.12073372aaENSP00000459933.1
 
Protein coding
-A5PKV6 -GENCODE basic
ERCC4-002ENST00000462862.172135aaENSP00000461322.1
 
Nonsense mediated decay
-I3L4K0 -CDS 5' incomplete
ERCC4-007ENST00000574194.158375aaENSP00000461883.1
 
Nonsense mediated decay
---CDS 5' incomplete
ERCC4-006ENST00000574781.1638No protein-
 
Processed transcript
----
ERCC4-004ENST00000389138.32106No protein-
 
Retained intron
----
ERCC4-005ENST00000576348.1604No protein-
 
Retained intron
----
ERCC4-008ENST00000573018.1523No protein-
 
Retained intron
----

Gene-based displays