Human (GRCh37.p13)
Description

excision repair cross-complementing rodent repair deficiency, complementation group 6-like 2 [Source:HGNC Symbol;Acc:26922]

Gene Synonyms

C9orf102, FLJ37706, RAD26L, SR278

Location

Chromosome 9: 98,637,983-98,776,842 forward strand.

GRCh37:CM000671.1

About this gene

This gene has 10 transcripts (splice variants), 2 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000288985.7ERCC6L2-0014564712aaENSP00000288985.7
 
Protein coding
CCDS35072Q5T890 NM_001010895.2GENCODE basic
ENST00000437817.1ERCC6L2-2023691523aaENSP00000416286.1
 
Protein coding
Q5T890 -GENCODE basic
ENST00000320486.5ERCC6L2-0062925522aaENSP00000320939.5
 
Protein coding
--CDS 5' incomplete
ENST00000407474.3ERCC6L2-2012109531aaENSP00000384365.3
 
Protein coding
A4D997 -GENCODE basic
ENST00000402838.2ERCC6L2-007546182aaENSP00000384215.2
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000426805.1ERCC6L2-00449882aaENSP00000395345.1
 
Protein coding
--CDS 5' incomplete
ENST00000479391.2ERCC6L2-005284954aaENSP00000473877.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000456993.1ERCC6L2-0021822365aaENSP00000409751.1
 
Nonsense mediated decay
F2Z2R4 --
ENST00000466840.1ERCC6L2-0033586No protein-
 
Processed transcript
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ENST00000470362.1ERCC6L2-008468No protein-
 
Processed transcript
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