H-Inv ID |
HIT000268499 |
H-Inv cluster ID |
HIX0004887
|
H-Inv protein ID |
HIP000072244
|
Accession number |
CR536563.1
|
CAGE tag ID |
NA
|
EST ID |
NA
|
Genomic location
|
Chromosome |
5 |
Location |
5q12.1
|
Position |
60170442-
60240835
|
Strand |
-
|
Transcript feature
|
NO;
|
Coding potential
|
Protein coding;
|
Definition |
DNA excision repair protein ERCC-8; Cockayne syndrome WD repeat protein CSA; |
Similarity category
|
Category: Identical to known human protein(Category I).
|
Identical to known human protein (Q13216)
[Identity/coverage = 100.0%/100.0%] to
Homo sapiens (Human). protein.
|
Gene family / group |
NA
|
Gene symbol/name |
HGNC symbol |
ERCC8
|
HGNC aliases |
"Cockayne syndrome 1 (classical)", "excision repair cross-complementing rodent repair deficiency, complementation group 8"
|
HGNC name |
excision repair cross-complementation group 8
|
DDBJ |
CKN1
|
UniProt |
ERCC8
|
EC number |
NA
|
KEGG metabolic pathway |
NA
|
PubMed ID |
7664335;
12732143;
14661080;
14702039;
15489334;
15744458;
16751180;
16916636;
19329487;
19894250;
21406692;
22466612;
ALL;
|
Related H-InvDB links |
Similarity Search Tool
|
Database links |
RefSeq |
NA
|
Ensembl |
NA
|
Entrez Gene |
Entrez Gene ID:1161;
|
KEGG GENES |
KEGG GENES(1161);
|
GeneCard |
ERCC8;
*GeneCards is provided free to academic non-profit institutions.
|
etc |
Human-Gene diversity Of Life-style related Diseases;
|
Curation status |
Auto-annotated
|
Notes |
NA
|