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Observed CMAH gene variants (nsSNVs and indels), PROVEAN analyses, genotypes, and haplotypes in different purebred and non-pedigreed cats with blood types A, B and C.

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posted on 2018-09-20, 20:11 authored by Alexandra Kehl, Kevin Heimberger, Ines Langbein-Detsch, Sabine Boehmer, Karthik Raj, Elisabeth Mueller, Urs Giger

Observed CMAH gene variants (nsSNVs and indels), PROVEAN analyses, genotypes, and haplotypes in different purebred and non-pedigreed cats with blood types A, B and C.

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    CMAH genotyping schemevariant c .364CSNVPROVEANCMAH variants c .179G c .268TCytidine monophosphate-N-acetylneuraminic acid hydroxylaseCMAH coding regionsvariants c .1322delTtype C erythrocytestype B catstype Bblood type compatibilityblood type BCMAH variant c .268Tc .142G c .268TCMAH coding regionc .933delA cause frameshiftsAB blood group systemvariant c .179G resultsconverts N-acetylneuraminic acid

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