OMIA:001300-93934 : Hereditary multiple malformation in Coturnix japonica (Japanese quail)

Categories: Mortality / aging (incl. embryonic lethal)

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive

Considered a defect: yes

Key variant known: no

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2020). OMIA:001300-93934: Online Mendelian Inheritance in Animals (OMIA) [dataset].


1998 Tsudzuki, M., Nakane, Y., Wada, A. :
Hereditary multiple malformation in Japanese quail - a possible powerful animal model for morphogenetic studies Journal of Heredity 89:24-31, 1998. Pubmed reference: 9487677.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Frank Nicholas on 15 May 2020