Gene List
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Gene ID Gene Sybmol Position Dog Disease Name #Variants #Exon #BioProject #GWAS catalog
ENSCAFG00000001141 NDRG1 Chr13 : 29689072 - 29746038 (-) Polyneuropathy, NDRG1-related (OMIA002120)
18476 105 62 -
ENSCAFG00000001218 HSD17B3 Chr1 : 70550942 - 70585751 (+) Sex reversal: XY female, SRY-positive (OMIA001601)
- 18 - -
ENSCAFG00000001392 PNPLA1 Chr12 : 5377869 - 5417577 (+) Ichthyosis, PNPLA1-related (OMIA001588)
3272 21 62 -
ENSCAFG00000001406 MKLN1 Chr14 : 5636382 - 5799833 (-) Acrodermatitis, lethal (OMIA002146)
6221 33 62 2
ENSCAFG00000001424 PLA2G6 Chr10 : 26498600 - 26558894 (+) Neuroaxonal dystrophy, PLA2G6-related (OMIA002105)
11174 76 62 -
ENSCAFG00000001433 PLEC Chr13 : 37442695 - 37502589 (-) Epidermolysis bullosa, simplex, PLEC-related (OMIA002080)
18563 327 62 -
ENSCAFG00000001478 TYRP1 Chr11 : 33317645 - 33335498 (+) Coat colour, brown, TYRP1-related (OMIA001249)
3683 9 62 -
ENSCAFG00000001630 MYH9 Chr10 : 28063626 - 28124814 (+) May-Hegglin anomaly (OMIA001608)
17182 244 62 -
ENSCAFG00000001722 PRPH2 Chr12 : 11299236 - 11316175 (-) Retinal degeneration II (OMIA001244)
1412 38 62 -
ENSCAFG00000001833 ABCB4 Chr14 : 13542668 - 13614146 (-) Gallbladder mucoceles (OMIA001524)
2525 33 62 -
ENSCAFG00000001835 ABCB1 Chr14 : 13644042 - 13743053 (-) Multidrug resistance 1 (OMIA001402)
17673 145 62 -
ENSCAFG00000001917 CNGA1 Chr13 : 43831107 - 43845271 (-) Progressive retinal atrophy, CNGA1-related (OMIA001977)
2806 33 62 -
ENSCAFG00000002028 VLDLR Chr1 : 91241810 - 91271886 (+) Cerebellar hypoplasia, VLDLR-associated (OMIA001947)
3680 71 62 -
ENSCAFG00000002065 KIT Chr13 : 47107802 - 47192057 (+) Gastrointestinal stromal tumor (OMIA001516)
Coat colour, white spotting, KIT-related (OMIA001737)
4106 62 62 -
ENSCAFG00000002065 KIT Chr13 : 47107802 - 47192057 (+) Gastrointestinal stromal tumor (OMIA001516)
Coat colour, white spotting, KIT-related (OMIA001737)
4106 62 62 -
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