ERCC5
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Homo sapiens |
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ERCC5 is differentially expressed in 244 experiments: 106 organism parts: liver, lung, ... (104 more);, 141 disease states: normal, acute myeloid leukemia, ... (139 more);, 77 cell types 314 cell lines 35 compound treatments and 62 other conditions. |
| Synonyms |
ERCM2, XPGC |
| Orthologs |
Ercc5
(Mus musculus)
ercc5
(Danio rerio)
ERCC5
(Gallus gallus)
Q3B7N6_BOVIN
(Bos taurus)
Ercc5
(Rattus norvegicus)
RAD2
(Saccharomyces cerevisiae)
mus201
(Drosophila melanogaster)
ercc5
(Xenopus laevis)
ERCC5
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
response to UV, DNA binding, nucleotide-excision repair, protein binding, DNA repair, double-stranded DNA binding, nuclease activity, negative regulation of apoptosis, protein N-terminus binding, metal ion binding, single-stranded DNA binding, determination of adult lifespan, multicellular organism growth, nucleus, endodeoxyribonuclease activity, protein homodimerization activity, endonuclease activity, nucleoplasm, catalytic activity, transcription-coupled nucleotide-excision repair, DNA-directed RNA polymerase II, holoenzyme, holo TFIIH complex, response to UV-C, UV protection, bubble DNA binding, nucleotide-excision repair, DNA incision, 3'-to lesion, nucleotide-excision repair, DNA damage removal |
| Gene Ontology ID |
GO:0003677, GO:0003690, GO:0003697, GO:0008340, GO:0003824, GO:0009411, GO:0042803, GO:0005515, GO:0047485, GO:0005634, GO:0005654, GO:0004518, GO:0004519, GO:0004520, GO:0043066, GO:0046872, GO:0006289, GO:0006281, GO:0035264, GO:0016591, GO:0010225, GO:0009650, GO:0005675, GO:0006295, GO:0006283, GO:0000405, GO:0000718 |
| InterPro Term |
XPG_DNA_repair_N, XPG/RAD2_endonuclease, XPGC_DNA_repair, XPGC_Rad_DNA_repair, HhH2 |
| InterPro ID |
IPR001044, IPR006086, IPR006085, IPR006084, IPR008918 |
| Ensembl Family |
ENSFM00570000851135 |
| Ensembl Family Description |
DNA REPAIR COMPLEMENTING XP G CELLS EC_3.1.-.- XERODERMA PIGMENTOSUM GROUP G COMPLEMENTING |
| EMBL-Bank ID |
AF255442, AF255440, AF255441, AF255439, AF255438, AF255436, AF255437, AF255434, AF255435, AF255433, AF255431, L20046, X69978, D16305, X71342, X71341, AL157769, AF550128, BC031522, AF462447 |
| HGNC Symbol |
ERCC5 |
| Entrez Gene ID |
2073, 100533467 |
| Ensembl Protein ID |
ENSP00000365121, ENSP00000365122, ENSP00000404887, ENSP00000347978, ENSP00000436083, ENSP00000442117 |
| UniGene ID |
Hs.713587, Hs.258429 |
| UniProt Accession |
Q86UB2, Q9HD60, P28715, F2Z2A1, F8WDY3 |
| Description |
excision repair cross-complementing rodent repair deficiency, complementation group 5 [Source:HGNC Symbol;Acc:3437] |
| Ensembl Gene ID |
ENSG00000134899 |
| RefSeq ID |
NP_000114, NM_000123, NP_001191354, NM_001204425 |
| Ensembl Transcript ID |
ENST00000355739, ENST00000375958, ENST00000375955, ENST00000375954, ENST00000418659, ENST00000481099, ENST00000472247, ENST00000535557, ENST00000472151 |
| Gene-Disease Assocation |
CEREBROOCULOFACIOSKELETAL SYNDROME 1; COFS1, XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG |
| Design Element |
ENST00000418659, ENST00000535557, 2064_g_at, ENST00000375955, ENST00000375954, ENST00000355739, gnf1h02115_x_at, ENST00000472151, ENST00000375958, X69978_at, g4503600_3p_at, ENST00000472247, 2063_at, ENST00000481099, 202414_at |
| Search EB-eye |
ENSG00000134899
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