MBG 2040 Study Guide - Midterm Guide: Edwards Syndrome, Dna Replication, Down Syndrome

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9:7 = complementation (multiple genes, when homo rec. , produce the same pheno. Individuals complement each other by being homo rec. on different genes so they produce the wildtype) 9:3:4 = recessive epistasis (homo rec. masks other gene aa/b- = aa/bb) 12:3:1 = dominant epistatis (dom. allele at one gene masks other a-/b- = a-/bb) If a trait/phenotype is rare and autosomal recessive then a person who marries into the family, unless there is reason to believe otherwise, is considered to be homozygous dominant. If a trait/phenotype is rare and autosomal dominant then a person who marries into the family, unless there is reason to believe otherwise, is considered to be heterozygous. Null alleles = non-functional or absence of protein. Hypomorphic alleles = poorly functioning protein or less amount produced of normal protein. Dominant hypermorphic alleles = negative phenotypic impact due to excess amount or over-active normal protein.

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