TLS Online TPP Program

#Id: 8197

#Section 3: Genetics, Cellular and Molecular Biology

Zellweger syndrome

Autosomal recessive Mutations in any of a dozen different peroxins, the most common being Pex1, cause an impairment in peroxisomal protein import.

TLS Online TPP Program

#Id: 8157

#Section 3: Genetics, Cellular and Molecular Biology

TLS Online TPP Program

#Id: 9147

#Section 3: Genetics, Cellular and Molecular Biology

TLS Online TPP Program

#Id: 8517

#Section 3: Genetics, Cellular and Molecular Biology

Other proteins function with dynein & involved in regulating the activity of dynein during brain development:

LIS1 and NudE

TLS Online TPP Program

#Id: 8976

#Section 3: Genetics, Cellular and Molecular Biology

Rate of evolution = Number of amino acid different / Total time

Hint:  Total time = 2xT

Rate of Change per amino acid per year = rate of evolution / total amino acid