C57BL/6N-Atm1Brd Del(10Map3k5-Map7)2Kcl Rhox13tm1a(KOMP)Wtsi/WtsiH[cc]

Status

Available to order

EMMA IDEM:13795
International strain nameC57BL/6N-Atm1Brd Del(10Map3k5-Map7)2Kcl Rhox13tm1a(KOMP)Wtsi/WtsiH[cc]
Alternative nameRhyme, Del(10Map3k5-Map7)2Kcl
Strain typeSpontaneous
Allele/Transgene symbolDel(10Map3k5-Map7)2Kcl,
Gene/Transgene symbolDel(10Map3k5-Map7)2Kcl

Information from provider

ProviderKaren Steel
Provider affiliationKing
Genetic informationThe causative mutation is a 36.7kb deletion, g.10:20116294_20153024del, which includes the last 9 exons of Map3k5 and the first exon of Map7 (Del(10Map3k5-Map7)2Kcl or Rhyme). It arose in a colony carrying the targeted mutation Rhox13tm1a(KOMP)Wtsi, and this allele may still exist in the background.
Phenotypic informationHomozygous:
Homozygotes for the Rhyme deletion had raised thresholds for detecting responses to sounds at high frequencies at 4 weeks old, and the hearing loss progressed with age. The males are sterile.

Heterozygous:
No obvious defect.
Breeding historyThe Rhyme mutation arose spontaneously in a colony carrying the targeted mutation Rhox13tm1a(KOMP)Wtsi, and this allele may still exist in the background. It was maintained within a closed colony on a C57BL/6N background for several years by heterozygous intercrosses or heterozygous males mated with homozygous females.
References
  • Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.;Lewis Morag A, Ingham Neil J, Chen Jing, Pearson Selina, Di Domenico Francesca, Rekhi Sohinder, Allen Rochelle, Drake Matthew, Willaert Annelore, Rook Victoria, Pass Johanna, Keane Thomas, Adams David J, Tucker Abigail S, White Jacqueline K, Steel Karen P, ;2022;BMC biology;20;67; 35296311
Homozygous fertilefemales only
Homozygous viableyes
Homozygous matings requiredno
Immunocompromisednot known

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom

Literature references

  • Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.;Lewis Morag A, Ingham Neil J, Chen Jing, Pearson Selina, Di Domenico Francesca, Rekhi Sohinder, Allen Rochelle, Drake Matthew, Willaert Annelore, Rook Victoria, Pass Johanna, Keane Thomas, Adams David J, Tucker Abigail S, White Jacqueline K, Steel Karen P, ;2022;BMC biology;20;67; 35296311

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