ERCC2

GENERAL INFORMATION

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Gene name

ERCC2

Gene description

Excision repair cross-complementation group 2

Protein class

Cancer-related genes
Disease related genes
Enzymes
Potential drug targets
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

General nuclear expression with additional cytoplasmic expression in several tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA038057 , CAB005375
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

ERCC2 (HGNC Symbol)

Synonyms

EM9, MAG, MGC102762, MGC126218, MGC126219, TFIIH, XPD

Description

Excision repair cross-complementation group 2 (HGNC Symbol)

Entrez gene summary

The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]

Chromosome

19

Cytoband

q13.32

Chromosome location (bp)

45349837 - 45370918

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000104884 (version 78.38)

Entrez gene

2068

UniProt

P18074 (UniProt - Evidence at protein level)

neXtProt

NX_P18074

Antibodypedia

ERCC2 antibodies


PROTEIN BROWSER

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ENST00000391941
 
ENST00000391944
 
ENST00000391945
 
ENST00000485403
 
ENST00000586131
 
ENST00000586856
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ERCC2-001 ENSP00000375809
ENST00000391945
P18074
Show all »
Show » Show » 760 86.9 No 0
ERCC2-002 ENSP00000464887
ENST00000586131
K7EIT8
Show all »
Show » Show » 292 33.4 No 0
ERCC2-003 ENSP00000466998
ENST00000586856
K7ENL1
Show all »
Show » Show » 109 12.7 No 0
ERCC2-005 ENSP00000375805
ENST00000391941
A8MX75
Show all »
Show » Show » 706 80.5 No 0
ERCC2-006 ENSP00000431229
ENST00000485403
P18074
Show all »
Show » Show » 405 46.3 No 0
ERCC2-201 ENSP00000375808
ENST00000391944
E7EVE9
Show all »
Show » Show » 682 77.9 No 0