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Allele : Mitf<mi-enu22(398)> melanogenesis associated transcription factor; microphthalmia enu 22(398)

Primary Identifier  MGI:6162028 Allele Type  Chemically induced (ENU)
Attribute String  Null/knockout Gene  Mitf
Strain of Origin  Not Specified Is Recombinase  false
Is Wild Type  false
molecularNote  This mutation was induced by treatment with ethylnitrosourea as part of a genetic screen performed at the Novartis Institute for Functional Genomics. Sequence analysis shows that the mutation is a C-to-T change at nucleotide position 205 of the cDNA, which introduces a stop codon in exon 2A, changing glutamine at position 26 of the MITF protein to STOP.
  • mutations:
  • Single point mutation
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

5 Publication categories