Male mice heterozygote for the Insrtm1Dac allele were treated with ENU and their offspring were screened for impaired glucose tolerance. One line derived from this screen was found to have a single A to G mutation at nucleotide position 1,025 of this gene locus. This corresponded to a tyrosine to cysteine substitution at amino acid 123 (Y123C), which lies in the highly conserved HMG-binding domain. Allelic complementation suggests that this is a functionally null allele. (J:141688)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count