ramets (224 20m Dote;__Pesiod: Sex-Linked Traits Worksheet 1) Albinism sa recessive atoscmal genetic disorder that causes the complet ox partial absence of ‘pigmeni in the skin, hair and eyes. Fill athe Punnet square and determine the expected genotypic Tats ffom crossing homozygove recessive snd heterozygous dominant prea aS A [Po |e] a foo_joo cwcoipes:_ fa co. Cceatypi Rata: 2 Phenotypes Currier Adio eof kis with disorder U7, t6ofeanierkids: 5D "To 2) ReGen ar nds recive socked shremoons) gets andr where 2s gc orlngeyelow) wav ons ine ee re eal or nope of cee eer aR ct leur cad dete i expec nope tod pheno fom cosing {soul nal eas female oho carer fo clandns x x x yest s A ¥ hy [ty pee fe XL hy ie l pot) cma a ih ends ama enala cari fenal fide wih ducer 25 [Cie tir ade female 13) Color blindness i a recessive sex-linked genetic dssider located on the X chromosome. Fil nthe ‘Punnett square fora cross of male with color blindness and a normal female x * Aches! RS x bty|x cope yh Circle all phenotype(s 0 male with clocblindness ‘wot kids with disorder: (57. Circe their genders) male/female 4 Color blindness is a recessive sex-Hnked genetic disoder located on the X chromosome, Filia the ‘Punnett square fora cross of male whois colorblind and a female whois a carsier fr color blindness, ee pee ee \ 4 ty (Leeann 2010,5) Color blindness is a recessive sex-linked genetic disorder located onthe X chromosome. Flin the FPnnet square fra css ofa nannal wale an a ale who eoor blind. XL cmsonpen XX ye LOO) Ce | cileattpheootee: nomal mile, male wih slodindis, Dy | oy) asmnsLinmal sis femal ele wih clatindnen NOISY | recs wecece (Ya Cie ther ged final female 6) Color bindness is a recessive sex-inked genetic dsoeder located on the X chromosome, Flin the square fora cos of olor blind male and color bind female. LeeLee] cite at peep am >) Ln | moma female, amie female Smale > . Y DALEY) Sets ofa nr pan aa 7 ain sete is ition mira : et abs, p= Trak Harel to CAC NDSEOL #)Enpan why aleve more rink cde foals Berauy wv yu owe | Ke cone Ly PEARL ie fy a Male vo Vos, ate Acme Ayer oa A for a Samale do bau Re Alsorder, ‘© Leon Plmelae 2010Sex-Linked Pedigrees Workshect Background Information: Pedigres ae used to trace a gene as itis passed down from ‘generation to generation. The squares represent a male andthe circles epreseot «female. the ‘examples on this handow, the shaded czcles and squazes will represent having the disorder. ‘Male sure to read each question to find oat if disorder is caused by dominant alleles or recessive alleles. A personcan bea camer of tat, meaning they have heterozygous alleles, 1) Hemophilia is a recessive sex-linked disorder located on the X chromosome where a person's ‘body cannot cantrol blood cloting or coagulation. Writ in the geootypes onthe line next to/ ‘below each indivi. x G @ 2" ou ‘Far all phenotype questions, onthe frst line write: male or female andthe second ine write: norma, carier, hemophilia. 2) ‘Whats the phenotype of individual 27 Female corner 3) What isthe phenotype of individual 4? Ne Senet Lt 4) What isthe phenotype of individuals? XC rm yo nophica 5) Wats the phenotype ofindviaal VN Nocyval 6) Whats the phenotype of individual 92 ely, Carn 7) Whats the phenotype ofindividoal 107) Narrel 8) Whatis the phenotype of individual 11? CONUS Ot 9) What ia the phenotype of individual 127, vaale. Carne ‘©beean Plas. 2011