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Allele : Mocs2<tm1Geno> molybdenum cofactor synthesis 2; targeted mutation 1, Genoway

Primary Identifier  MGI:7493923 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Mocs2
Transmission  Germline Strain of Origin  C57BL/6
Is Recombinase  false Is Wild Type  false
molecularNote  The Mocs2A subunit mutation, a C to T change at position 88 (c.88C>T) resulting in a glutamine to a termination codon at amino acid 30 (p.Q30*) was introduced in exon 3. In addition, a loxP-flanked neomycin cassette was inserted downstream of exon 3. This is a variant found in patients with molybdenum cofactor deficiency type B.
  • mutations:
  • Single point mutation
  • synonyms:
  • Mocs2A Q30X,
  • Mocs2A Q30X
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories