OMIA:001901 : Haplotype with homozygous deficiency, RNASEH2B-related |
Categories: Mortality / aging (incl. embryonic lethal)
Possible human homologues (MIM numbers): 610181 (trait) , 610326 (gene)
Cross-species summary: Phenes previously called ‘Abortion due to halplotype ….. ’ or ‘Abortion (embryonic lethality)’ , have been renamed to ‘Haplotype with homozygous deficiency, …’ or a phene name that is descriptive of the phenotype observed in homozygous affected animals [14/1/2022
Species in which this phene is found:
taurine cattle (Bos taurus)
Edit History
- Created by Frank Nicholas on 04 Jan 2014
- Changed by Frank Nicholas on 04 Mar 2017
- Changed by Imke Tammen2 on 25 Sep 2021
- Changed by Imke Tammen2 on 18 Jan 2022