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genetically-located traits & disorders
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chromosome 2
· pyruvate kinase deficiency (gene PKLR)
chromosome 5
· early-onset cone-rod dystrophy (gene NPHP4)
· non-ESPS/ESPS (gene Mc1R)
· [possibly] von Willebrand's (gene vWA1)
chromosome 9
· mucopolysaccharidosis IIIa (gene SGSH)
· non-harlequin/harlequin (gene PSMB7)
chromosome 10
· non-dapple/dapple (gene SILV)
chromosome 11
· black/chocolate (gene TyrP1)
chromosome 12
· narcolepsy (gene Hcrtr2)
chromosome 13
· wirehair/non-wirehair (gene RSPO2)
chromosome 15
· cone-rod dystrophy type 1 (gene RPGRIP1)
chromosome 16
· KSES/non-KSES & brindle (gene CBD103)
· [probably] myotonia (gene CLCN1)
· [possibly] rear dewclaws (gene LMBR1)
chromosome 17
· [possibly] von Willebrand's (gene VWF)
chromosome 18
· hypochondroplasia (gene FGF4)
chromosome 20
· [possibly] non-parti/parti (gene MITF)
chromosome 21
· juvenile-onset neuronal ceroid lipofuscinosis (gene TpP1)
· osteogenesis imperfecta (gene SerpInh1)
chromosome 24
· ASPS/points (gene ASP)
chromosome 25
· non-dilute/dilute (gene MLPH)
chromosome 27
· curly/straight (gene KRT17)
chromosome 32
· shorthair/longhair (gene FGF5)
chromosome 35
· Lafora's (gene Epm2b)
chromosome 37
· [possibly] collie eye anomaly (gene NHEJ1)
chromosome 38
· ticking/plating & roaning/plating
chromosome X
· [probably] hemophilia A (gene FVIII)
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All TSL posts are copyright by their respective authors and may not be used or reproduced without their express permission.
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