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15 phene records found |
[show instead gene records] |
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| OMIA ID | Phene | Species Scientific Name | Species Common Name | Gene | Year Key Mutation First Reported | Date Last Modified |
|---|---|---|---|---|---|---|
| OMIA:002538-9483 | Alzheimer disease, APP-related | Callithrix jacchus | white-tufted-ear marmoset | 2023-12-18 | ||
| OMIA:002493-9483 | Alzheimer disease, PSEN1-related | Callithrix jacchus | white-tufted-ear marmoset | 2023-12-18 | ||
| OMIA:000033-9483 | Alzheimer-like disease, generic | Callithrix jacchus | white-tufted-ear marmoset | 2025-01-05 | ||
| OMIA:000038-9483 | Amyloidosis, AA | Callithrix jacchus | white-tufted-ear marmoset | 2011-11-27 | ||
| OMIA:002473-9483 | Ataxia, spinocerebellar, ATXN3-related | Callithrix jacchus | white-tufted-ear marmoset | ATXN3 | 2020 | 2023-12-10 |
| OMIA:002328-9483 | Behaviour | Callithrix jacchus | white-tufted-ear marmoset | 2023-01-13 | ||
| OMIA:002686-9483 | Colour vision, deficiency | Callithrix jacchus | white-tufted-ear marmoset | 2023-05-05 | ||
| OMIA:000299-9483 | Dwarfism, generic | Callithrix jacchus | white-tufted-ear marmoset | 2021-01-08 | ||
| OMIA:000344-9483 | Epilepsy | Callithrix jacchus | white-tufted-ear marmoset | 2022-02-13 | ||
| OMIA:002455-9483 | Fragile X syndrome, FMR1-related | Callithrix jacchus | white-tufted-ear marmoset | 2023-12-10 | ||
| OMIA:001364-9483 | Fused labia | Callithrix jacchus | white-tufted-ear marmoset | 2005-09-06 | ||
| OMIA:000428-9483 | Haemochromatosis | Callithrix jacchus | white-tufted-ear marmoset | 2013-05-03 | ||
| OMIA:002379-9483 | Parkinson disease, LRRK2-related | Callithrix jacchus | white-tufted-ear marmoset | 2023-12-18 | ||
| OMIA:002378-9483 | Parkinson disease, SNCA-related | Callithrix jacchus | white-tufted-ear marmoset | 2023-12-18 | ||
| OMIA:000944-9483 | Spongiform encephalopathy, susceptibility/resistance to | Callithrix jacchus | white-tufted-ear marmoset | 2020-05-15 |