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84 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:002317-9986 | Abnormal gait, retinal dysplasia, cataracts, RORB-related | Oryctolagus cuniculus | rabbit | RORB | 2021 | 2022-10-31 |
| OMIA:000017-9986 | Adrenal insufficiency, congenital, CYP11A1-related | Oryctolagus cuniculus | rabbit | CYP11A1 | 1993 | 2023-09-29 |
| OMIA:002007-9986 | Agenesis, renal | Oryctolagus cuniculus | rabbit | 2016-05-03 | ||
| OMIA:001243-9986 | Alkaptonuria | Oryctolagus cuniculus | rabbit | 2018-05-31 | ||
| OMIA:002600-9986 | Amelogenesis imperfecta, FAM83H-related | Oryctolagus cuniculus | rabbit | FAM83H | 2022 | 2023-12-18 |
| OMIA:001551-9986 | Brachycephaly | Oryctolagus cuniculus | rabbit | 2024-03-06 | ||
| OMIA:000155-9986 | C3 deficiency | Oryctolagus cuniculus | rabbit | 2005-07-16 | ||
| OMIA:001624-9986 | C6 deficiency | Oryctolagus cuniculus | rabbit | 2011-10-11 | ||
| OMIA:000156-9986 | C8 deficiency | Oryctolagus cuniculus | rabbit | 2013-06-17 | ||
| OMIA:000162-9986 | Cardiomyopathy, dilated | Oryctolagus cuniculus | rabbit | 2009-10-27 | ||
| OMIA:002212-9986 | Cardiomyopathy, hypertrophic, MYH7-related | Oryctolagus cuniculus | rabbit | 2021-04-21 | ||
| OMIA:002331-9986 | Cardiomyopathy, TNNI3-related | Oryctolagus cuniculus | rabbit | 2024-10-18 | ||
| OMIA:002308-9986 | Cardiomyopathy, X-linked dilated | Oryctolagus cuniculus | rabbit | 2021-01-28 | ||
| OMIA:002735-9986 | Cataract, GJA8-related | Oryctolagus cuniculus | rabbit | GJA8 | 2016 | 2023-12-18 |
| OMIA:002394-9986 | Cleft lip, GADD45G-related | Oryctolagus cuniculus | rabbit | 2023-12-18 | ||
| OMIA:000197-9986 | Cleft palate | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:000201-9986 | Coat colour, agouti | Oryctolagus cuniculus | rabbit | ASIP | 2010 | 2023-03-06 |
| OMIA:001249-9986 | Coat colour, brown, TYRP1-related | Oryctolagus cuniculus | rabbit | TYRP1 | 2014 | 2023-03-06 |
| OMIA:000031-9986 | Coat colour, dilution, MLPH-related | Oryctolagus cuniculus | rabbit | MLPH | 2013 | 2023-03-06 |
| OMIA:000209-9986 | Coat colour, dominant white | Oryctolagus cuniculus | rabbit | 2022-10-28 | ||
| OMIA:001199-9986 | Coat colour, extension | Oryctolagus cuniculus | rabbit | MC1R | 2006 | 2023-03-06 |
| OMIA:000202-9986 | Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related | Oryctolagus cuniculus | rabbit | TYR | 2000 | 2023-03-06 |
| OMIA:001168-9986 | Coronal suture synostosis | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:001224-9986 | Craniosynostosis | Oryctolagus cuniculus | rabbit | 2021-08-22 | ||
| OMIA:001794-9986 | Cystic fibrosis | Oryctolagus cuniculus | rabbit | CFTR | 2020 | 2024-02-21 |
| OMIA:000279-9986 | Diabetes mellitus | Oryctolagus cuniculus | rabbit | 2023-12-10 | ||
| OMIA:001709-9986 | Difference of sexual development, DMRT1-related | Oryctolagus cuniculus | rabbit | DMRT1 | 2023 | 2023-12-18 |
| OMIA:000312-9986 | Dysautonomia | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:002157-9986 | Ectodermal dysplasia-9 | Oryctolagus cuniculus | rabbit | HOXC13 | 2019 | 2023-12-10 |
| OMIA:000327-9986 | Ehlers-Danlos syndrome, generic | Oryctolagus cuniculus | rabbit | 2005-07-16 | ||
| OMIA:000344-9986 | Epilepsy | Oryctolagus cuniculus | rabbit | 2016-04-29 | ||
| OMIA:002687-9986 | Fleece variation (fine vs coarse) | Oryctolagus cuniculus | rabbit | 2024-04-07 | ||
| OMIA:001528-9986 | Fleece variation (woolly vs hairy) | Oryctolagus cuniculus | rabbit | 2023-10-16 | ||
| OMIA:001461-9986 | Gangliosidosis, GM2, type I (B variant) | Oryctolagus cuniculus | rabbit | 2013-05-03 | ||
| OMIA:000411-9986 | Glaucoma, generic | Oryctolagus cuniculus | rabbit | 2022-09-17 | ||
| OMIA:000439-9986 | Hair, long | Oryctolagus cuniculus | rabbit | FGF5 | 2023 | 2023-11-15 |
| OMIA:000459-9986 | Hernia, diaphragmatic | Oryctolagus cuniculus | rabbit | 2011-10-18 | ||
| OMIA:000473-9986 | Hip dysplasia | Oryctolagus cuniculus | rabbit | 2024-08-20 | ||
| OMIA:000487-9986 | Hydrocephalus | Oryctolagus cuniculus | rabbit | 2016-04-29 | ||
| OMIA:000493-9986 | Hydrops foetalis | Oryctolagus cuniculus | rabbit | 2016-04-29 | ||
| OMIA:000499-9986 | Hypercholesterolaemia | Oryctolagus cuniculus | rabbit | 2023-12-10 | ||
| OMIA:002329-9986 | Hypercholesterolaemia, PCSK9-related | Oryctolagus cuniculus | rabbit | 2023-12-18 | ||
| OMIA:001160-9986 | Hyperlipidaemia | Oryctolagus cuniculus | rabbit | LDLR | 1986 | 2013-05-17 |
| OMIA:002490-9986 | Hyperlipidaemia/atherosclerosis, APOC3-related | Oryctolagus cuniculus | rabbit | 2023-12-18 | ||
| OMIA:002063-9986 | Hyperlipidaemia/atherosclerosis, APOE-related | Oryctolagus cuniculus | rabbit | APOE | 2016 | 2023-12-18 |
| OMIA:000511-9986 | Hyperthyroidism | Oryctolagus cuniculus | rabbit | 2022-09-17 | ||
| OMIA:001542-9986 | Hypophosphatemic rickets, autosomal recessive, 1 | Oryctolagus cuniculus | rabbit | 2023-12-18 | ||
| OMIA:000540-9986 | Hypotrichosis, generic | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:002855-9986 | Hypoxanthine guanine phosphoribosyltransferase deficiency | Oryctolagus cuniculus | rabbit | 2024 | 2024-05-21 | |
| OMIA:001687-9986 | Inflammatory bowel disease | Oryctolagus cuniculus | rabbit | 2024-04-19 | ||
| OMIA:001404-9986 | Leptin concentration | Oryctolagus cuniculus | rabbit | 2024-09-02 | ||
| OMIA:002334-9986 | Long QT syndrome, KCNE1-related | Oryctolagus cuniculus | rabbit | 2021-04-21 | ||
| OMIA:002333-9986 | Long QT syndrome, KCNH2-related | Oryctolagus cuniculus | rabbit | 2021-04-21 | ||
| OMIA:002332-9986 | Long QT syndrome, KCNQ1-related | Oryctolagus cuniculus | rabbit | 2021-04-21 | ||
| OMIA:000618-9986 | Macrostomus | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:000621-9986 | Malignant hyperthermia | Oryctolagus cuniculus | rabbit | 2023-01-13 | ||
| OMIA:000628-9986 | Marfan syndrome | Oryctolagus cuniculus | rabbit | FBN1 | 2018 | 2023-12-10 |
| OMIA:000629-9986 | Megacolon | Oryctolagus cuniculus | rabbit | 2015-12-31 | ||
| OMIA:002688-9986 | Microcephaly, YIPF5-related | Oryctolagus cuniculus | rabbit | YIPF5 | 2023 | 2023-12-18 |
| OMIA:002242-9986 | Muscular dystrophy, ANO5-related | Oryctolagus cuniculus | rabbit | 2023-12-18 | ||
| OMIA:000683-9986 | Muscular hypertrophy (double muscling) | Oryctolagus cuniculus | rabbit | 2023-12-12 | ||
| OMIA:000715-9986 | Neuroaxonal dystrophy, generic | Oryctolagus cuniculus | rabbit | 2011-05-27 | ||
| OMIA:001962-9986 | Neuronal ceroid lipofuscinosis, 7 | Oryctolagus cuniculus | rabbit | MFSD8 | 2024 | 2024-05-09 |
| OMIA:001258-9986 | Obesity | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:000753-9986 | Osteodystrophy | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:000755-9986 | Osteopetrosis | Oryctolagus cuniculus | rabbit | 2016-04-29 | ||
| OMIA:000783-9986 | Pelger-Huet anomaly | Oryctolagus cuniculus | rabbit | 2022-11-23 | ||
| OMIA:000807-9986 | Polycystic kidney disease | Oryctolagus cuniculus | rabbit | 2011-05-27 | ||
| OMIA:001213-9986 | Premature senesence | Oryctolagus cuniculus | rabbit | LMNA | 2019 | 2024-01-18 |
| OMIA:001566-9986 | Rex coat | Oryctolagus cuniculus | rabbit | LIPH | 2011 | 2016-05-03 |
| OMIA:002441-9986 | Short QT syndrome, KCNH2-related | Oryctolagus cuniculus | rabbit | 2023-12-18 | ||
| OMIA:000933-9986 | Spina bifida | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:000944-9986 | Spongiform encephalopathy, susceptibility/resistance to | Oryctolagus cuniculus | rabbit | 2020-05-15 | ||
| OMIA:002067-9986 | Syndactyly, type Ia | Oryctolagus cuniculus | rabbit | 2016-10-30 | ||
| OMIA:000965-9986 | Syringomyelia | Oryctolagus cuniculus | rabbit | 2016-05-03 | ||
| OMIA:000985-9986 | Teat / nipple, number | Oryctolagus cuniculus | rabbit | 2021-01-13 | ||
| OMIA:001013-9986 | Torticollis | Oryctolagus cuniculus | rabbit | 2022-10-29 | ||
| OMIA:000770-9986 | Tremor, X-linked | Oryctolagus cuniculus | rabbit | PLP1 | 1994 | 2023-03-06 |
| OMIA:002078-9986 | Tyrosinaemia, type I | Oryctolagus cuniculus | rabbit | 2023-12-18 | ||
| OMIA:002624-9986 | Usher syndrome, USH2A-related | Oryctolagus cuniculus | rabbit | 2023-12-18 | ||
| OMIA:001041-9986 | Ventricular septal defect | Oryctolagus cuniculus | rabbit | 2016-04-28 | ||
| OMIA:001056-9986 | Von Willebrand disease, generic | Oryctolagus cuniculus | rabbit | 2005-09-06 | ||
| OMIA:001230-9986 | XY sex reversal, SRY-related | Oryctolagus cuniculus | rabbit | SRY | 2017 | 2023-12-18 |
| OMIA:001079-9986 | Yellow fat | Oryctolagus cuniculus | rabbit | BCO2 | 2015 | 2023-03-06 |