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Gene ENSMUSG00000054051 (Ercc6)
Chromosomal location
Chr 14: 33326707 - 33394175 (+)
Description
excision repair cross-complementing rodent repair deficiency, complementation group 6 Gene [Source:MGI Symbol;Acc:MGI:1100494]
RefSeq_dna
NM_001081221 
RefSeq_peptide
NP_001074690.1 
UniGene
Mm.318310 Mm.405507 
MGI
MGI:1100494 
Uniprot/SPTREMBL
A3KMN2 Q8C851 
Human Ortholog
ENSG00000032514 (ERCC6)
Omim 133540 - COCKAYNE SYNDROME, TYPE B  214150 - CEREBROOCULOFACIOSKELETAL SYNDROME 1  278800 - DE SANCTIS-CACCHIONE SYNDROME  600630 - UV-SENSITIVE SYNDROME  609413 - EXCISION-REPAIR CROSS-COMPLEMENTING, GROUP 6  
UniTrap UNI9729
Vector Insertion
Chr 14: 33334246 - 33339334
Public Clones XG105 (baygenomics) A023C04 (ggtc)
Private Clones not available
Severity of mutation (?) Insertion after 15% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI9407
Vector Insertion
Chr 14: 33383618 - 33387991
Public Clones XH442 (baygenomics)
Private Clones not available
Severity of mutation (?) Insertion after 84% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI3308
Vector Insertion
Chr 14: 33389013 - 33389871
Public Clones AD0345 (sanger)
Private Clones not available
Severity of mutation (?) Insertion after 91% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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