ERCC1
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Homo sapiens |
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ERCC1 is differentially expressed in 339 experiments: 143 organism parts: heart, cerebellum, ... (141 more);, 173 disease states: normal, control, ... (171 more);, 111 cell types 447 cell lines 45 compound treatments and 83 other conditions. |
| Synonyms |
RAD10 |
| Orthologs |
Ercc1
(Rattus norvegicus)
ercc1
(Danio rerio)
ERCC1_BOVIN
(Bos taurus)
Ercc1
(Mus musculus)
RAD10
(Saccharomyces cerevisiae)
Ercc1
(Drosophila melanogaster)
ercc1
(Xenopus laevis)
ENSCAFG00000023351
(Canis familiaris)
ENSCAFG00000004448
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
oogenesis, response to oxidative stress, DNA binding, nucleotide-excision repair, protein binding, DNA repair, cytoplasm, cell proliferation, damaged DNA binding, negative regulation of apoptosis, spermatogenesis, male gonad development, protein domain specific binding, multicellular organismal aging, single-stranded DNA binding, double-strand break repair, response to abiotic stimulus, nuclear chromosome, telomeric region, multicellular organism growth, response to nutrient, nucleus, DNA recombination, germ cell development, hydrolase activity, endonuclease activity, protein C-terminus binding, nucleoplasm, response to DNA damage stimulus, response to X-ray, chromosome organization, embryonic organ development, syncytium formation, post-embryonic hemopoiesis, transcription-coupled nucleotide-excision repair, negative regulation of telomere maintenance, nucleotide-excision repair complex, pyrimidine dimer repair by nucleotide-excision repair, structure-specific DNA binding, UV protection, isotype switching, nucleotide-excision repair, DNA incision, 3'-to lesion, nucleotide-excision repair, DNA incision, 5'-to lesion, cell development, single-stranded DNA specific endodeoxyribonuclease activity, replicative cell aging, response to sucrose stimulus, mitotic recombination, nucleotide-excision repair, DNA damage removal |
| Gene Ontology ID |
GO:0003684, GO:0003677, GO:0003697, GO:0008283, GO:0008022, GO:0010259, GO:0010165, GO:0009628, GO:0007283, GO:0007281, GO:0008584, GO:0051276, GO:0007584, GO:0016787, GO:0048477, GO:0005515, GO:0005737, GO:0005634, GO:0005654, GO:0004519, GO:0006979, GO:0006974, GO:0043066, GO:0019904, GO:0000784, GO:0006302, GO:0006310, GO:0006289, GO:0006281, GO:0035264, GO:0009650, GO:0009744, GO:0048568, GO:0001302, GO:0000014, GO:0048468, GO:0006949, GO:0000720, GO:0000109, GO:0006295, GO:0006296, GO:0006283, GO:0043566, GO:0045190, GO:0032205, GO:0035166, GO:0006312, GO:0000718 |
| Ensembl Family Description |
DNA EXCISION REPAIR ERCC 1 |
| InterPro Term |
HhH_motif, DNA_repair_Rad10 |
| InterPro ID |
IPR000445, IPR004579 |
| Ensembl Family |
ENSFM00500000271240 |
| Description |
excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence) [Source:HGNC Symbol;Acc:3433] |
| UniProt Accession |
Q8WWH8, P07992, Q96S40, B3KRR0, Q7Z7F5, F5GWP0 |
| EMBL-Bank ID |
AF433652, AC092309, AC138534, M28650, M26163, AF001925, BT019806, M13194, AK092039, AB069681, CH471126, BC052813, BC008930, AF512555, AC138128, AC139353 |
| HGNC Symbol |
ERCC1 |
| Entrez Gene ID |
2067 |
| RefSeq ID |
NP_001974, NM_001983, NM_001166049, NP_973730, NM_202001, NP_001159521 |
| Ensembl Protein ID |
ENSP00000013807, ENSP00000394875, ENSP00000400434, ENSP00000300853, ENSP00000345203 |
| Ensembl Gene ID |
ENSG00000012061 |
| Ensembl Transcript ID |
ENST00000340192, ENST00000300853, ENST00000428893, ENST00000423698, ENST00000013807 |
| UniGene ID |
Hs.435981 |
| Gene-Disease Assocation |
CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4 |
| Design Element |
ENST00000013807, g4503598_3p_a_at, 1902_at, Hs.25523.0.A1_3p_at, 203719_at, ENST00000423698, M13194_at, 203720_s_at, 36519_at, ENST00000428893, 228131_at, 1878_g_at, 64168_r_at, ENST00000340192, ENST00000300853, Hs.25523.0.A1_3p_x_at, 64167_f_at |
| Search EB-eye |
ENSG00000012061
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