TLS Online TPP Program

#Question id: 4910


For a trait known to be caused by a mitochondrial gene variant, there may be an occasional female that can transmit different phenotypes to her progeny on an apparently random basis. What situation might you suspect?

#Unit 8. Inheritance Biology
  1. She is heterozygous for this trait.

  2. She displays heteroplasmy for this trait.

  3. She displays a low rate of mutation.

  4. She is the product of a somatic mutation

More Questions
TLS Online TPP Program

#Question id: 5346

#Unit 8. Inheritance Biology

The following typical pedigree illustrates the key point that affected children are born to unaffected parents: Which of the following is correct statement?

TLS Online TPP Program

#Question id: 5347

#Unit 8. Inheritance Biology

The inheritance of a given disorder is recorded in small families shown below: Based on the above limited information, which one of the following inheritance pattern best explains the observations?

TLS Online TPP Program

#Question id: 5348

#Unit 8. Inheritance Biology

Miniature wings (Xm) in Drosophila result from an X-linked allele that is recessive to the allele for long wings (XL). Following different cross with resulting progeny were possible

Male parent

Female parent

Heterozygous

Male offspring

Female offspring

Long wings

XLY

Long wing

XL Xm

       A

B

Miniature wings

XmY

Long wing

XL Xm

C

D

Which of the following above offspring is not possible to carry miniature wings?

TLS Online TPP Program

#Question id: 5349

#Unit 8. Inheritance Biology

The following is the inheritance pattern of a trait under observation:

(i) The trait often follow cris cross inheritance 

(iii) Unaffected father born to affected daughter

The trait is likely to be

TLS Online TPP Program

#Question id: 5350

#Unit 8. Inheritance Biology

Which of the following most probable mode of genetic disorder?

TLS Online TPP Program

#Question id: 5351

#Unit 8. Inheritance Biology

Consider the accompanying pedigree of a rare autosomal recessive disease, PKU. (Assume individual coming from outside that is homozygous for normal allele) What is the probability of child showing trait of A and B individuals?