AVM v1, released 02-OCT-22

A manually curated database of aerosol-transmitted virus mutations, human diseases, and drugs

Mutation detail:


Mutation site A63G
Virus Measles virus
Mutation level Amino acid Level
Gene/protein/region type H
Gene ID 1489801
Country Canada
Mutation type nonsynonymous mutation
Genotype/subtype/clade D6
Sample Human
Variants -
Viral reference sequence AF266288.1
Drug/antibody/vaccine -
Transmissibility -
Transmission mechanism -
Pathogenicity -
Pathogenicity mechanism -
Immune escape mutation -
Immune escape mechanism -
RT-PCR primers probes -

Protein detail:


Protein name Hemagglutinin Protein
Uniprot protein ID P08362
Protein length 617 amino acids
Protein description Hemagglutinin Protein attaches the virus to cell receptors and thereby initiating infection. Binding of H protein to the receptor induces a conformational change that allows the F protein to trigger virion/cell membranes fusion. May use human CD46 and/or SLAMF1 as receptors for viral entry into the cell. The high degree of interaction between H and MCP/CD46 results in down-regulation of the latter from the surface of infected cells, rendering them more sensitive to c3b-mediated complement lysis.

Literature information:


Pubmed ID 30291564
Clinical information No
Disease SSPE(Subacute sclerosing panencephalitis)
Published year 2018
Journal Journal of NeuroVirology
Title Genetic characterization of measles virus genotype D6 subacute sclerosing panencephalitis case, Alberta, Canada
Author K Pabbaraju,K Fonseca,S Wong,M W Koch,J T Joseph
Evidence Amino acid changes unique to the SSPE_Alberta_2014 included I8T, F11L, L42P, A63G, D132N, N282S, T331I, and E565K.