Figure 1
- ID
- ZDB-FIG-210301-142
- Publication
- Chrystal et al., 2021 - The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning
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Allelic consequence of foxc1-targeted CRISPR/Cas9 mutagenesis: (A) a schematic representation of foxc1aua1017 and foxc1bua1018 mutations, with 7 and 40 base pair deletions (yellow highlighting) upstream of the DNA-binding Forkhead domain; (B) the predicted sequences of the first 40 amino acids translated from wildtype (WT) and mutant proteins with sequence identity (black highlighting), where the foxc1aua1017 allele produces a truncated 39-residue protein with loss of sequence homology from amino acid 10 and the foxc1bua1018 allele produces a truncated 28-residue protein with loss of sequence homology from amino acid 19; and (C) PCR genotyping from the gDNA template resolving the respective deletions in foxc1a and foxc1b. (FHD, Forkhead domain; UTR, untranslated region; CDS, coding sequence.). |