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Gene ENSMUSG00000037169 (Mycn)
Chromosomal location
Chr 12: 12942905 - 12948642 (-)
Description
v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian) Gene [Source:MGI Symbol;Acc:MGI:97357]
RefSeq_dna
NM_008709 
RefSeq_peptide
NP_032735.3 
UniGene
Mm.16469 Mm.400380 
MGI
MGI:97357 
Uniprot/SWISSPROT
P03966 
Uniprot/SPTREMBL
Q3UII1 Q810L7 Q923F4 
Human Ortholog
ENSG00000134323 (MYCN)
Omim 164280 - FEINGOLD SYNDROME  602585 - MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE  
UniTrap UNI10908
Vector Insertion
Chr 12: 12947293 - 12948441
Public Clones P147D06 (ggtc)
Private Clones not available
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI24675
Vector Insertion
Chr 12: 12944417 - 12946415
Public Clones not available
Private Clones OST210340 (lexicon)
Severity of mutation (?) Insertion after 57% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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