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OMIA:001815-9544 : Autism spectrum disorder in Macaca mulatta (Rhesus monkey)

In other species: zebra finch

Categories: Behaviour / neurological phene

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 209850 (trait) , 300425 (trait) , 300495 (trait) , 300496 (trait) , 300847 (trait) , 606053 (trait) , 607373 (trait) , 608049 (trait) , 609378 (trait) , 610676 (trait) , 610836 (trait) , 610838 (trait) , 610908 (trait) , 611015 (trait) , 611016 (trait) , 612100 (trait) , 613410 (trait) , 613436 (trait) , 614671 (trait) , 615032 (trait) , 615091 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

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. (2023). OMIA:001815-9544: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

2023 Garner, J.P., Talbot, C.F., Del Rosso, L.A., McCowan, B., Kanthaswamy, S., Haig, D., Capitanio, J.P., Parker, K.J. :
Rhesus macaque social functioning is paternally, but not maternally, inherited by sons: potential implications for autism. Mol Autism 14:25, 2023. Pubmed reference: 37480043. DOI: 10.1186/s13229-023-00556-3.

Edit History


  • Created by Imke Tammen2 on 26 Jul 2023