| Primary Identifier | MGI:1856276 | Allele Type | Spontaneous |
| Gene | Gli3 | Inheritance Mode | Semidominant |
| Strain of Origin | C3H/HeJ | Is Recombinase | false |
| Is Wild Type | false |
| description | Genbank ID for this allele: AF418601 Phenotypic Similarity to Human Syndrome: lambdoid suture craniosynostosis in homozygous mice (J:163175) |
| molecularNote | Genomic sequencing and PCR analysis identified the mutation as a 51.5 kb deletion. The deleted region contains all Gli3 coding sequences 3' to exon 9, which includes sequences encoding some, but not all, of the zinc finger domains. This deletion results in the expression of an abnormal transcript that fuses Gli3 sequences to an exon belonging to an apparent LTR/MaLR repetitive element. However, this transcript lacks the sequences required for normal GLI3 activity. |
