Human (GRCh37.p13)
Description

excision repair cross-complementing rodent repair deficiency, complementation group 3 [Source:HGNC Symbol;Acc:3435]

Gene Synonyms

BTF2, GTF2H, RAD25, TFIIH, XPB, XPBC

Location

Chromosome 2: 128,014,866-128,051,752 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 10 transcripts (splice variants) and is associated with 68 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000493187.2ERCC3-2012920718aaENSP00000444796.1
 
Protein coding
G3V1S1 -GENCODE basic
ENST00000285398.2ERCC3-0012750782aaENSP00000285398.2
 
Protein coding
CCDS2144G3V1S1 P19447 NM_000122.1GENCODE basic
ENST00000456257.1ERCC3-011563188aaENSP00000408901.1
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000445889.1ERCC3-004292071aaENSP00000390888.1
 
Nonsense mediated decay
F2Z2V4 --
ENST00000426778.1ERCC3-005291671aaENSP00000415335.1
 
Nonsense mediated decay
F2Z2V4 --
ENST00000491292.1ERCC3-0064018No protein-
 
Retained intron
---
ENST00000494464.1ERCC3-0031367No protein-
 
Retained intron
---
ENST00000462306.1ERCC3-002963No protein-
 
Retained intron
---
ENST00000460485.1ERCC3-010815No protein-
 
Retained intron
---
ENST00000490062.1ERCC3-007576No protein-
 
Retained intron
---