Additional file 11 of Searching for homozygous haplotype deficiency in Manech Tête Rousse dairy sheep revealed a nonsense variant in the MMUT gene affecting newborn lamb viability

  1. Ben Braiek, Maxime 1
  2. Moreno-Romieux, Carole 1
  3. André, Céline
  4. Astruc, Jean-Michel 2
  5. Bardou, Philippe 3
  6. Bordes, Arnaud 1
  7. Debat, Frédéric 1
  8. Fidelle, Francis
  9. Granado-Tajada, Itsasne 4
  10. Hozé, Chris
  11. Plisson-Petit, Florence 1
  12. Rivemale, François 1
  13. Sarry, Julien 1
  14. Tadi, Némuel 1
  15. Woloszyn, Florent 1
  16. Fabre, Stéphane 1
  1. 1 Federal University of Toulouse Midi-Pyrénées
  2. 2 Institut de l’Elevage
    info

    Institut de l’Elevage

    París, Francia

    ROR https://ror.org/01csjkt09

  3. 3 National Research Institute for Agriculture, Food and Environment
  4. 4 Instituto Vasco de Investigación y Desarrollo Agrario
    info

    Instituto Vasco de Investigación y Desarrollo Agrario

    Derio, España

    ROR 03rf31e64

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Editor: figshare

Ano de publicación: 2024

Tipo: Dataset

CC BY 4.0

DOI: 10.6084/M9.FIGSHARE.26687157 lock_openAcceso aberto editor

Resumo

Additional file 11: Table S7. List of the 408 protein coding genes located in the five MTRDHH regions extended by 1 Mb on each side. Mouse knock-out (KO) phenotypes and association with mammalian disorders were extracted for each gene from several databases: MGI: www.informatics.jax.org ; IMPC: https://www.mousephenotype.org ; OMIM: Online Mendelian Inheritance in Man ( https://omim.org ) and OMIA: Online Mendelian Inheritance in Animal ( https://omia.org ). For mouse KO phenotypes associated with lethality, the affected developmental stages is indicated by 1 (0, no lethality).

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