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. 2020 Feb 12;10:2431. doi: 10.1038/s41598-020-59110-3

Table 3.

Genes with disease and its’ mutation in mandrill.

Gene name Full name Position Wildtype AA Mutation AA Disease Description
ALAD Aminolevulinate Dehydratase 59 K N Amyotrophic lateral sclerosis
CIITA Class II Major Histocompatibility Complex Transactivator 500 G A Multiple sclerosis
CRB1 Crumbs Cell Polarity Complex Component 1 959 G S Retinitis pigmentosa
IL4R Interleukin 4 Receptor 75 I V Asthma, atopic
MCPH1 Microcephalin 1 761 A V Cranial volume
NPHS2 NPHS2 Stomatin Family Member, Podocin 192 I V Nephrotic syndrome
TP53BP1 Tumor Protein P53 Binding Protein 1 353 D E Lung cancer