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. 2021 Mar 30;11:7159. doi: 10.1038/s41598-021-86200-7

Table 1.

Description and diseases of 41 cats for WES evaluation.

No Id Breed Sex Disease/Trait Gene(s)
1 19725 Lykoi F Lykoi HR
2 13230 Mixed Breed F Bengal PRA/Bobbed tail KIF3B/HES7
3 14056 Mixed Breed M Persian PRA/Long AIPL1/FGF5
4 17994 Mixed Breed F Hydrocephalus GDF7
5 19067 Munchkin F Dwarfism/Dominant White UGDH/KIT
6 5012 Oriental M Lymphoma Unknown
7 20382 Peterbald M Hairless LPAR6a
8 11615 Random Bred M Dominant White KIT
9 18528 Random Bred M Spotting KIT
10 20424 Siberian F Long/Cardiac disease FGF5/Candidate
11 22550 Bengal F Polyneuropathy Unknown
12 20957 Devon Rex U Papilloma virus Unknown
13 22752 Devon Rex M Neurological disorder Unknown
14–15 21983/21464 Ojos Azules 1M:1F Ojos Azules Unknown
16 20964 Oriental F Cardiac disease Unknown
17 22728 Random bred F Cystinuria SLC3A1a
18 20617 Random Bred M Neuronal ceroid lipofuscinosis CLN6a
19 20948 Random Bred M Cinnamic acid urea Unknown
20 21153 Random Bred M Ambulatory paraparesis Unknown
21 22287 Random Bred F Myotonia congenita Unknown
22 22397 Random Bred M Neurological disorder Unknown
23 22505 Random Bred M Cardiac disease Unknown
24 22623 Random Bred U Pycnodysostosis Candidate
25 22740 Random Bred F Epidemolysis bullosa Unknown
26–27 22741/22742 Random Bred 1F:1M Eyelid coloboma Unknown
28 22751 Random Bred M Ehlers-Danlos Unknown
29–30 22763/22764 Random Bred 2F Hypothyroidism Candidate
31–32 22761/22762 Savannah 2M Hypovitaminosis D Unknown
33 21984 Scottish Fold F Cardiac disease Candidate
34–35 20384/20385 Selkirk Rex 1F:1U Seizures Unknown
36 20953 Siamese F Cardiac disease Candidate
37 22622 Siberian U PKD PKD2a
38 22711 Singapura F Hypovitaminosis D Candidate
39–40 8641/8642 Tennessee Rex 1F:1M Rexoid hair coat Unknown
41 6623 Oriental M Lymphoma Unknown
41 14 breeds 19F:18M:4U ~ 31 diseases and traits

A complete description of diseases and traits for entire cohort. Candidate genes are potential genes that been identified with less evidence of a causal mutations.

U unknown sex, F female, M male.

aMutations as tentative causal variants for diseases presented.