MEDIUM
Earn 100

Define albinism.

Important Questions on Inheritance

MEDIUM
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype

Fill in the blank with the correct answer from the bracket.

Mutations in the _____ gene cause haemophilia (F8, HTT, Le, TYR)

EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
The F8 gene abnormal allele result in less or no production of _____.(factor I / factor VIII / factor II)
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
The abnormal polypeptide synthesised by the HBB gene consists of _____ instead of CTT.
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
The abnormal form of recessive allele of Le gene causes formation of _____ instead of threonine.
MEDIUM
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Which of the following is an autosomal dominant genetic disorder?
MEDIUM
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Which of the following is a recessive sex-linked genetic disorder? 
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
The gene responsible for producing tyrosinase is shown as 
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Cotyledons are also called-
MEDIUM
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Explain the symptoms of Huntington's disease.
HARD
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Explain the symptoms of haemophilia.
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Explain the synthesis of F8 gene and its importance.
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Explain the role of HTT gene and disease associated with it.
MEDIUM
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Sickle cell anaemia is a dominant autosomal disorder.
MEDIUM
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Huntington's disease is a sex-linked disease.
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
HBB gene is located on the long arm of the chromosome 11.
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
TYR gene is present on the long arm of the chromosome 11.
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
Gibberellin can stimulate the growth of plants that are normally dwarf.
EASY
Biology>Genetics and Evolution P2>Inheritance>Genes, Proteins and Phenotype
The HTT gene is located on chromosome 11.