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Allele : Del(Y)1H deletion, Chr Y, 1 Harwell

Primary Identifier  MGI:3043691 Allele Type  Spontaneous
Gene  Del(Y)1H Strain of Origin  BALB/cJToxCrcH and RIII
Is Recombinase  false Is Wild Type  false
molecularNote  This Y Chr deletion resulted from asymmetric recombination during male meiosis between the short arm of a Y Chr (Yp) of BALB/c origin and an X Chr carrying Tp(Y)1CtSxr-a. Whereas Sry (sex determining region of Chr Y) and 16 other single-copy genes and pseudogenes on Yp appear intact by Southern blot or PCR analysis, the unequal exchange resulted in deletion of 3-4 Mb, including 90% of the Rbmy (RNA binding motif protein, Y Chr) repeat sequence family, which resides between Sry and the centromere and normally comprises at least 50 copies. Sry transcripts are undetectable by semiquantitative RT-PCR analysis of RNA from the genital ridges of 11.5 day post coitus (dpc) XYDel(Y)1H and XXYDel(Y)1H embryos; in contrast, transcripts from Kdm5d, which maps distal to Sry between Zfy1 and Zfy2, are similarly abundant in XYDel(Y)2H and XY 11.5 dpc genital ridges.
  • mutations:
  • Intergenic deletion
  • synonyms:
  • Del1Ct,
  • Del1Ct,
  • Y<d1>,
  • Y<d-1>,
  • Y<d1>,
  • Y<d-1>
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1 Feature

Trail: Allele

Genome

0 Expresses

1 Mutation Involves

Trail: Allele

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

18 Publication categories

Trail: Allele