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... See more...

Aliases for ERCC2 Gene

Aliases for ERCC2 Gene

  • ERCC Excision Repair 2, TFIIH Core Complex Helicase Subunit 2 3 5
  • Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 2 3
  • General Transcription And DNA Repair Factor IIH Helicase Subunit XPD 3 4
  • TFIIH Basal Transcription Factor Complex Helicase XPB Subunit 2 3
  • TFIIH Basal Transcription Factor Complex 80 KDa Subunit 3 4
  • Xeroderma Pigmentosum Group D-Complementing Protein 3 4
  • Excision Repair Cross-Complementation Group 2 2 3
  • Basic Transcription Factor 2 80 KDa Subunit 3 4
  • Xeroderma Pigmentosum Complementary Group D 2 3
  • DNA Repair Protein Complementing XP-D Cells 3 4
  • DNA Excision Repair Protein ERCC-2 3 4
  • TFIIH 80 KDa Subunit 3 4
  • TFIIH Subunit XPD 3 4
  • TFIIH P80 3 4
  • BTF2 P80 3 4
  • CXPD 3 4
  • XPD 3 4
  • Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 Protein 2
  • TFIIH Basal Transcription Factor Complex Helicase XPD Subunit 3
  • TFIIH Basal Transcription Factor Complex Helicase Subunit 3
  • EC 3.6.4.12 4
  • EC 3.6.1 52
  • COFS2 3
  • TFIIH 3
  • TTD1 3
  • XPDC 4
  • EM9 3
  • TTD 3

External Ids for ERCC2 Gene

Previous HGNC Symbols for ERCC2 Gene

  • XPD

Previous GeneCards Identifiers for ERCC2 Gene

  • GC19M046497
  • GC19M046245
  • GC19M050529
  • GC19M050546
  • GC19M045854
  • GC19M042287

Summaries for ERCC2 Gene

Entrez Gene Summary for ERCC2 Gene

  • 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]

CIViC Summary for ERCC2 Gene

  • ERCC2 functions as a DNA repair gene involved in separating the double helix via 5’-3’ helicase activity. It forms a part of the transcription factor II Human (TFIIH) complex and is ATP-dependent. The TFIIH complex is known to be involved in the nucleotide excision repair pathway (NER) which can repair DNA damage caused by chemotherapeutic treatment and basal transcription. ERCC2 variants have been observed in a variety of cancers. A number of studies have suggested ERCC2 variants can act as biomarkers to predict response to neoadjuvant treatment, and cancer prognosis. Additionally the Lys751Gln polymorphism has been observed to increase risk in a number of cancer types; however, results have been conflicting.

GeneCards Summary for ERCC2 Gene

ERCC2 (ERCC Excision Repair 2, TFIIH Core Complex Helicase Subunit) is a Protein Coding gene. Diseases associated with ERCC2 include Trichothiodystrophy 1, Photosensitive and Xeroderma Pigmentosum, Complementation Group D. Among its related pathways are Formation of HIV-1 elongation complex containing HIV-1 Tat and Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3. Gene Ontology (GO) annotations related to this gene include nucleic acid binding and protein C-terminus binding. An important paralog of this gene is RTEL1.

UniProtKB/Swiss-Prot Summary for ERCC2 Gene

  • ATP-dependent 5'-3' DNA helicase, component of the general transcription and DNA repair factor IIH (TFIIH) core complex, which is involved in general and transcription-coupled nucleotide excision repair (NER) of damaged DNA and, when complexed to CAK, in RNA transcription by RNA polymerase II. In NER, TFIIH acts by opening DNA around the lesion to allow the excision of the damaged oligonucleotide and its replacement by a new DNA fragment. The ATP-dependent helicase activity of XPD/ERCC2 is required for DNA opening. In transcription, TFIIH has an essential role in transcription initiation. When the pre-initiation complex (PIC) has been established, TFIIH is required for promoter opening and promoter escape. Phosphorylation of the C-terminal tail (CTD) of the largest subunit of RNA polymerase II by the kinase module CAK controls the initiation of transcription. XPD/ERCC2 acts by forming a bridge between CAK and the core-TFIIH complex. Involved in the regulation of vitamin-D receptor activity. As part of the mitotic spindle-associated MMXD complex it plays a role in chromosome segregation. Might have a role in aging process and could play a causative role in the generation of skin cancers.

Gene Wiki entry for ERCC2 Gene

Additional gene information for ERCC2 Gene

No data available for Tocris Summary , PharmGKB "VIP" Summary , Rfam classification and piRNA Summary for ERCC2 Gene

Genomics for ERCC2 Gene

GeneHancer (GH) Regulatory Elements for ERCC2 Gene

Promoters and enhancers for ERCC2 Gene
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around ERCC2 on UCSC Golden Path with GeneCards custom track

Cistromic (ChIP-Seq) regulation report from SPP (The Signaling Pathways Project) for ERCC2

Top Transcription factor binding sites by QIAGEN in the ERCC2 gene promoter:
  • AML1a
  • CBF(2)
  • En-1
  • GR
  • GR-alpha
  • Ik-2
  • LCR-F1
  • MZF-1
  • p53
  • ZID

Genomic Locations for ERCC2 Gene

Genomic Locations for ERCC2 Gene
chr19:45,349,837-45,370,918
(GRCh38/hg38)
Size:
21,082 bases
Orientation:
Minus strand
chr19:45,853,095-45,874,176
(GRCh37/hg19)
Size:
21,082 bases
Orientation:
Minus strand

Genomic View for ERCC2 Gene

Genes around ERCC2 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
ERCC2 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for ERCC2 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for ERCC2 Gene

Proteins for ERCC2 Gene

  • Protein details for ERCC2 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    P18074-ERCC2_HUMAN
    Recommended name:
    General transcription and DNA repair factor IIH helicase subunit XPD
    Protein Accession:
    P18074
    Secondary Accessions:
    • Q2TB78
    • Q2YDY2
    • Q7KZU6
    • Q8N721

    Protein attributes for ERCC2 Gene

    Size:
    760 amino acids
    Molecular mass:
    86909 Da
    Cofactor:
    Name=Mg(2+); Xref=ChEBI:CHEBI:18420;
    Cofactor:
    Name=[4Fe-4S] cluster; Xref=ChEBI:CHEBI:49883;
    Quaternary structure:
    • Component of the 7-subunit TFIIH core complex composed of XPB/ERCC3, XPD/ERCC2, GTF2H1, GTF2H2, GTF2H3, GTF2H4 and GTF2H5, which is active in NER. The core complex associates with the 3-subunit CDK-activating kinase (CAK) module composed of CCNH/cyclin H, CDK7 and MNAT1 to form the 10-subunit holoenzyme (holo-TFIIH) active in transcription. The interaction with GTF2H2 results in the stimulation of the 5'-->3' helicase activity (PubMed:9771713, PubMed:9852112). Component of the MMXD complex, which includes CIAO1, ERCC2, CIAO2B, MMS19 and SLC25A5 (PubMed:20797633). Interacts with CIAO1 and CIAO2B; the interaction WITH CIAO2B is direct (PubMed:23891004). Interacts with ATF7IP (PubMed:19106100). Interacts directly with MMS19 (PubMed:23585563).
    • (Microbial infection) Interacts with Epstein-Barr virus EBNA2.
    SequenceCaution:
    • Sequence=AAM45142.1; Type=Erroneous gene model prediction; Evidence={ECO:0000305};

    Three dimensional structures from OCA and Proteopedia for ERCC2 Gene

    Alternative splice isoforms for ERCC2 Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for ERCC2 Gene

Selected DME Specific Peptides for ERCC2 Gene

P18074:
  • AIKPVFERF
  • SRILKARLE
  • LCIHPEV
  • KLIYCSRTVPEIE
  • LEMPSGTGKT
  • FDEAHNIDNVCI
  • SVARGKV
  • RGKVSEGIDF
  • YSYHYLLDPKIA
  • FDAMRHAAQC
  • GIYNLDDLKA
  • LLVYFPY
  • HHYGRAVIMFG
  • GWCPYFLAR
  • EAVPGSIRTAEHFLGFLRRLLEYVKWRLRVQHVVQESPPA
  • SLPHCRFYEEFD
  • DASLAIKPVF

Post-translational modifications for ERCC2 Gene

Antibody Products

  • Abcam antibodies for ERCC2

Domains & Families for ERCC2 Gene

Gene Families for ERCC2 Gene

HGNC:
Human Protein Atlas (HPA):
  • Cancer-related genes
  • Disease related genes
  • Enzymes
  • Potential drug targets
  • Predicted intracellular proteins

Protein Domains for ERCC2 Gene

Blocks:
  • ATP-dependent helicase, DEAH-box
  • Helicase c2
  • DEAD_2
  • Xeroderma pigmentosum group D protein signature
  • DEXDc2
  • Protein of unknown function DUF1227
InterPro:
ProtoNet:

Suggested Antigen Peptide Sequences for ERCC2 Gene

GenScript: Design optimal peptide antigens:
  • cDNA FLJ57462, highly similar to TFIIH basal transcription factor complex helicase subunit (EC 3.6.1.-) (B4E0F6_HUMAN)
  • Xeroderma pigmentosum group D-complementing protein (ERCC2_HUMAN)
  • ERCC2 protein (Q2TB79_HUMAN)

Graphical View of Domain Structure for InterPro Entry

P18074

UniProtKB/Swiss-Prot:

ERCC2_HUMAN :
  • Belongs to the helicase family. RAD3/XPD subfamily.
Family:
  • Belongs to the helicase family. RAD3/XPD subfamily.
genes like me logo Genes that share domains with ERCC2: view

Function for ERCC2 Gene

Molecular function for ERCC2 Gene

UniProtKB/Swiss-Prot Function:
ATP-dependent 5'-3' DNA helicase, component of the general transcription and DNA repair factor IIH (TFIIH) core complex, which is involved in general and transcription-coupled nucleotide excision repair (NER) of damaged DNA and, when complexed to CAK, in RNA transcription by RNA polymerase II. In NER, TFIIH acts by opening DNA around the lesion to allow the excision of the damaged oligonucleotide and its replacement by a new DNA fragment. The ATP-dependent helicase activity of XPD/ERCC2 is required for DNA opening. In transcription, TFIIH has an essential role in transcription initiation. When the pre-initiation complex (PIC) has been established, TFIIH is required for promoter opening and promoter escape. Phosphorylation of the C-terminal tail (CTD) of the largest subunit of RNA polymerase II by the kinase module CAK controls the initiation of transcription. XPD/ERCC2 acts by forming a bridge between CAK and the core-TFIIH complex. Involved in the regulation of vitamin-D receptor activity. As part of the mitotic spindle-associated MMXD complex it plays a role in chromosome segregation. Might have a role in aging process and could play a causative role in the generation of skin cancers.
UniProtKB/Swiss-Prot CatalyticActivity:
Reaction=ATP + H2O = ADP + H(+) + phosphate; Xref=Rhea:RHEA:13065, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:30616, ChEBI:CHEBI:43474, ChEBI:CHEBI:456216; EC=3.6.4.12;.
GENATLAS Biochemistry:
excision repair cross-complementing rodent repair defect in CHO cells (includes overlapping antisense sequence),complementation group 2,yeast RAD3 homolog (see XPD) mutations modify GTFIIH stoichiometry in XPD patients

Enzyme Numbers (IUBMB) for ERCC2 Gene

Phenotypes From GWAS Catalog for ERCC2 Gene

Gene Ontology (GO) - Molecular Function for ERCC2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000166 nucleotide binding IEA --
GO:0003676 nucleic acid binding IEA --
GO:0003677 DNA binding IEA --
GO:0003678 DNA helicase activity IEA --
GO:0003684 damaged DNA binding IBA 21873635
genes like me logo Genes that share ontologies with ERCC2: view
genes like me logo Genes that share phenotypes with ERCC2: view

Human Phenotype Ontology for ERCC2 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for ERCC2 Gene

MGI Knock Outs for ERCC2:

Animal Model Products

CRISPR Products

miRNA for ERCC2 Gene

miRTarBase miRNAs that target ERCC2

Clone Products

  • Addgene plasmids for ERCC2

No data available for Transcription Factor Targets and HOMER Transcription for ERCC2 Gene

Localization for ERCC2 Gene

Subcellular locations from UniProtKB/Swiss-Prot for ERCC2 Gene

Nucleus. Cytoplasm, cytoskeleton, spindle.

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for ERCC2 gene
Compartment Confidence
cytoskeleton 5
nucleus 5
cytosol 5
mitochondrion 2
plasma membrane 1
extracellular 1
peroxisome 1
endoplasmic reticulum 1
lysosome 1

Subcellular locations from the

Human Protein Atlas (HPA)
  • Nucleoplasm (3)
  • Cytosol (2)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for ERCC2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000439 transcription factor TFIIH core complex IEA --
GO:0005634 nucleus IEA,IDA 20797633
GO:0005654 nucleoplasm IDA,TAS --
GO:0005669 transcription factor TFIID complex IDA 27193682
GO:0005675 transcription factor TFIIH holo complex TAS 7663514
genes like me logo Genes that share ontologies with ERCC2: view

Pathways & Interactions for ERCC2 Gene

PathCards logo

SuperPathways for ERCC2 Gene

SuperPathway Contained pathways
1 Formation of HIV-1 elongation complex containing HIV-1 Tat
2 RNA Polymerase II Transcription Initiation And Promoter Clearance
.32
3 Transcription-Coupled Nucleotide Excision Repair (TC-NER)
4 Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3
5 HIV Life Cycle
.45
genes like me logo Genes that share pathways with ERCC2: view

Pathways by source for ERCC2 Gene

2 GeneGo (Thomson Reuters) pathways for ERCC2 Gene
  • Transcription Ligand-Dependent Transcription of Retinoid-Target genes
  • Transcription_P53 signaling pathway
1 Qiagen pathway for ERCC2 Gene
  • DNA Repair Mechanisms
2 Cell Signaling Technology pathways for ERCC2 Gene

SIGNOR curated interactions for ERCC2 Gene

Activates:
Is activated by:

Gene Ontology (GO) - Biological Process for ERCC2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000019 regulation of mitotic recombination IBA 21873635
GO:0000462 maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) IEA --
GO:0000717 nucleotide-excision repair, DNA duplex unwinding TAS,IBA --
GO:0001666 response to hypoxia IEA --
GO:0001701 in utero embryonic development IEA --
genes like me logo Genes that share ontologies with ERCC2: view

Drugs & Compounds for ERCC2 Gene

(23) Drugs for ERCC2 Gene - From: PharmGKB, HMDB, and Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Cisplatin Approved Pharma Inhibits DNA synthesis,chemotherapy drug, Potent pro-apoptotic anticancer agent; activates caspase-3, Platinum 3311
Docetaxel Approved, Investigational Pharma Microtubulin disassembly inhibitor, Tubulin and VEGF inhibitor, Taxanes 2273
Gemcitabine Approved Pharma Ribonucleotide reductase and DNA synthesis inhibitor, Nucleoside Analogs 2377
Oxaliplatin Approved, Investigational Pharma Antitumor agent, Platinum 1864
Bleomycin Approved, Investigational Pharma 175

(10) Additional Compounds for ERCC2 Gene - From: HMDB and Novoseek

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
ADP
  • 5'-Adenylphosphoric acid
  • Adenosine 5'-diphosphate
  • ADENOSINE-5'-diphosphATE
  • H3ADP
  • 5'-Adenylphosphate
Full agonist, Agonist, Partial agonist, Antagonist, Gating inhibitor 58-64-0
genes like me logo Genes that share compounds with ERCC2: view

Transcripts for ERCC2 Gene

mRNA/cDNA for ERCC2 Gene

2 REFSEQ mRNAs :
17 NCBI additional mRNA sequence :
13 Ensembl transcripts including schematic representations, and UCSC links to gene/alias where relevant :

CRISPR Products

Clone Products

  • Addgene plasmids for ERCC2

Alternative Splicing Database (ASD) splice patterns (SP) for ERCC2 Gene

ExUns: 1a · 1b ^ 2 ^ 3 ^ 4 ^ 5 ^ 6 ^ 7 ^ 8 ^ 9a · 9b · 9c ^ 10 ^ 11a · 11b ^ 12a · 12b ^ 13 ^ 14 ^ 15 ^ 16 ^ 17 ^ 18 ^ 19 ^ 20 ^ 21 ^
SP1: - - -
SP2: - -
SP3: - -
SP4:
SP5: - - - -
SP6:
SP7: - - -
SP8: -

ExUns: 22 ^ 23
SP1:
SP2:
SP3:
SP4:
SP5:
SP6:
SP7:
SP8:

Relevant External Links for ERCC2 Gene

GeneLoc Exon Structure for
ERCC2

Expression for ERCC2 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and SAGE for ERCC2 Gene

Protein differential expression in normal tissues from HIPED for ERCC2 Gene

This gene is overexpressed in Serum (23.0), Breast (9.1), Liver (7.3), and Monocytes (6.2).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, MaxQB, and MOPED for ERCC2 Gene



Protein tissue co-expression partners for ERCC2 Gene

- Elite partner

Transcriptomic regulation report from SPP (The Signaling Pathways Project) for ERCC2

SOURCE GeneReport for Unigene cluster for ERCC2 Gene:

Hs.487294

Phenotype-based relationships between genes and organs from Gene ORGANizer for ERCC2 Gene

Germ Layers:
  • ectoderm
  • endoderm
  • mesoderm
Systems:
  • cardiovascular
  • digestive
  • endocrine
  • immune
  • integumentary
  • lymphatic
  • nervous
  • reproductive
  • respiratory
  • skeletal muscle
  • skeleton
Regions:
Head and neck:
  • brain
  • cerebellum
  • chin
  • cranial nerve
  • ear
  • eye
  • eyelid
  • face
  • forehead
  • head
  • jaw
  • lip
  • mandible
  • maxilla
  • mouth
  • neck
  • nose
  • outer ear
  • pituitary gland
  • skull
  • tooth
Thorax:
  • breast
  • bronchus
  • chest wall
  • clavicle
  • lung
  • rib
  • rib cage
  • scapula
  • sternum
Abdomen:
  • intestine
  • large intestine
  • small intestine
Pelvis:
  • ovary
  • pelvis
  • penis
  • prostate
  • testicle
  • uterus
  • vagina
  • vulva
Limb:
  • ankle
  • arm
  • digit
  • elbow
  • femur
  • fibula
  • finger
  • foot
  • forearm
  • hand
  • hip
  • humerus
  • knee
  • lower limb
  • nail
  • radius
  • shin
  • shoulder
  • thigh
  • tibia
  • toe
  • ulna
  • upper limb
  • wrist
General:
  • blood
  • blood vessel
  • hair
  • peripheral nerve
  • peripheral nervous system
  • skin
  • spinal column
  • spinal cord
  • vertebrae
  • white blood cell
genes like me logo Genes that share expression patterns with ERCC2: view

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , mRNA Expression by UniProt/SwissProt and Evidence on tissue expression from TISSUES for ERCC2 Gene

Orthologs for ERCC2 Gene

This gene was present in the common ancestor of eukaryotes.

Orthologs for ERCC2 Gene

Organism Taxonomy Gene Similarity Type Details
chimpanzee
(Pan troglodytes)
Mammalia ERCC2 31 30
  • 99.3 (n)
OneToOne
platypus
(Ornithorhynchus anatinus)
Mammalia -- 31
  • 93 (a)
OneToMany
-- 31
  • 89 (a)
OneToMany
oppossum
(Monodelphis domestica)
Mammalia ERCC2 31
  • 93 (a)
OneToOne
cow
(Bos Taurus)
Mammalia ERCC2 31 30
  • 91.49 (n)
OneToOne
dog
(Canis familiaris)
Mammalia ERCC2 31 30
  • 91.36 (n)
OneToOne
mouse
(Mus musculus)
Mammalia Ercc2 17 31 30
  • 89.21 (n)
rat
(Rattus norvegicus)
Mammalia Ercc2 30
  • 88.51 (n)
tropical clawed frog
(Silurana tropicalis)
Amphibia ercc2 30
  • 71.01 (n)
zebrafish
(Danio rerio)
Actinopterygii ercc2 31 30
  • 72.48 (n)
OneToOne
zgc56365 30
African malaria mosquito
(Anopheles gambiae)
Insecta AgaP_AGAP002988 30
  • 67.44 (n)
fruit fly
(Drosophila melanogaster)
Insecta Xpd 31 32 30
  • 66.3 (n)
OneToOne
worm
(Caenorhabditis elegans)
Secernentea Y50D7A.2 32 30
  • 58.06 (n)
Y50D7A.11 31
  • 51 (a)
OneToOne
A. gosspyii yeast
(Ashbya gossypii)
Saccharomycetes AGOS_AGR114C 30
  • 56.42 (n)
K. lactis yeast
(Kluyveromyces lactis)
Saccharomycetes KLLA0C17776g 30
  • 52.22 (n)
baker's yeast
(Saccharomyces cerevisiae)
Saccharomycetes RAD3 31 30
  • 52.03 (n)
OneToOne
thale cress
(Arabidopsis thaliana)
eudicotyledons UVH6 30
  • 56.3 (n)
rice
(Oryza sativa)
Liliopsida Os05g0144800 30
  • 58.42 (n)
bread mold
(Neurospora crassa)
Ascomycetes NCU01625 30
  • 59.53 (n)
fission yeast
(Schizosaccharomyces pombe)
Schizosaccharomycetes rad15 30
  • 54.4 (n)
Species where no ortholog for ERCC2 was found in the sources mined by GeneCards:
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • chicken (Gallus gallus)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • lizard (Anolis carolinensis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for ERCC2 Gene

ENSEMBL:
Gene Tree for ERCC2 (if available)
TreeFam:
Gene Tree for ERCC2 (if available)
Aminode:
Evolutionary constrained regions (ECRs) for ERCC2: view image

Paralogs for ERCC2 Gene

Paralogs for ERCC2 Gene

(1) SIMAP similar genes for ERCC2 Gene using alignment to 8 proteins:

  • ERCC2_HUMAN
  • A8MX75_HUMAN
  • B4E0F6_HUMAN
  • E7EVE9_HUMAN
  • K7EIT8_HUMAN
  • K7EKF3_HUMAN
  • K7ENL1_HUMAN
  • Q2TB79_HUMAN
genes like me logo Genes that share paralogs with ERCC2: view

Variants for ERCC2 Gene

Sequence variations, with clinical significance, from ClinVar and Humsavar, with links to dbSNP for ERCC2 Gene

SNP ID Clinical significance and condition Chr 19 pos Variation AA Info Type
620626 Likely Pathogenic: Craniopharyngioma 45,357,481(-) GTGA/G INFRAME_DELETION
682343 Likely Benign: not provided 45,352,503(-) C/T INTRON_VARIANT
rs1052555 Benign: Xeroderma pigmentosum; not specified 45,352,266(-) G/A SYNONYMOUS_VARIANT
rs111562095 Not Provided: not specified 45,361,788(-) A/C INTRON_VARIANT
rs121913016 Pathogenic: Xeroderma pigmentosum, group D; Trichothiodystrophy 1, photosensitive; not specified. Trichothiodystrophy 1, photosensitive (TTD1) [MIM:601675]. Xeroderma pigmentosum complementation group D (XP-D) [MIM:278730] 45,357,368(-) G/Cp.Leu461Val MISSENSE_VARIANT

Additional dbSNP identifiers (rs#s) for ERCC2 Gene

Structural Variations from Database of Genomic Variants (DGV) for ERCC2 Gene

Variant ID Type Subtype PubMed ID
dgv1054e212 CNV gain 25503493
dgv29n64 CNV gain 17921354
dgv3606n100 CNV gain 25217958
esv3644502 CNV gain 21293372
esv3644504 CNV gain 21293372
nsv1063547 CNV gain 25217958
nsv1160648 CNV duplication 26073780
nsv1160649 CNV duplication 26073780
nsv428365 CNV gain+loss 18775914
nsv442466 CNV gain 18776908
nsv458711 CNV gain 19166990
nsv470146 CNV loss 18288195
nsv515681 CNV loss 19592680
nsv579867 CNV gain 21841781
nsv579868 CNV gain 21841781
nsv579869 CNV loss 21841781
nsv833844 CNV loss 17160897
nsv833845 CNV loss 17160897

Variation tolerance for ERCC2 Gene

Residual Variation Intolerance Score: 13.1% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 11.97; 93.64% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for ERCC2 Gene

Human Gene Mutation Database (HGMD)
ERCC2
SNPedia medical, phenotypic, and genealogical associations of SNPs for
ERCC2

SNP Genotyping and Copy Number Assay Products

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for ERCC2 Gene

Disorders for ERCC2 Gene

MalaCards: The human disease database

(37) MalaCards diseases for ERCC2 Gene - From: UniProtKB/Swiss-Prot, OMIM, ClinVar, GTR, Orphanet, DISEASES, Novoseek, and GeneCards