OMIA:001461-9888 : Gangliosidosis, GM2, type I (B variant) in Muntiacus muntjak (muntjak)

In other species: American flamingo , dog , pig , taurine cattle , sheep , rabbit

Categories: Lysosomal storage disease , Nervous system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 272800 (trait) , 606869 (gene)

Single-gene trait/disorder: yes

Mode of inheritance: Autosomal recessive

Disease-related: yes

Key variant known: no

Cross-species summary: Tay-Sachs disease

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Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2008). OMIA:001461-9888: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

References

Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.

2026 Suarez, D.A., Leal, A.F., Pachajoa, H., Granados-Villalobos, S., Espejo-Mojica, A.J., Seyrantepe, V., Alméciga-Díaz, C.J. :
Tay-Sachs disease models: From cellular and animal models to treatment perspectives. Mol Genet Metab 148:S1096-7192(26)00188-5:109905, 2026. Pubmed reference: 41880697. DOI: 10.1016/j.ymgme.2026.109905.
1999 Fox, J., Li, Y.T., Dawson, G., Alleman, A., Johnsrude, J., Schumacher, J., Homer, B. :
Naturally occurring G(M2) gangliosidosis in two Muntjak deer with pathological and biochemical features of human classical Tay-Sachs disease (type B G(M2) gangliosidosis) Acta Neuropathologica 97:57-62, 1999. Pubmed reference: 9930895.

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  • Created by Frank Nicholas on 20 Sep 2008