Amino acid replacement: M1467K.
T23811996A
M1506K | eIF4G2-PA; M1506K | eIF4G2-PC
M1467K
The reported amino acid location is based on an isoform with an intron that removes 39 aa from the first exon of RA.
Homozygous males do not undergo meiosis and show no recognisable meiotic or postmeiotic stages of spermatid differentiation. The testes contain cells in the gonial stage, cysts of primary spermatocytes and cysts of aberrant cells in a terminal stage that may represent degenerating primary spermatocytes.
eIF4G2nc32 is an enhancer of phenotype of βTub85Dunspecified
Fails to complement class I alleles at the βTub85D locus. Meiosis and spermatid differentiation occur in the sterile transheterozygotes.
Selected as: a mutation that fails to complement class I alleles at the βTub85D locus (either βTub85D3 or βTub85DDrv1) but does not map to the βTub85D locus.
Adult homozygous males show no βTub85D synthesis.