Hp1bp3^C57BL/6N
Spontaneous Allele Detail

Summary

• Symbol: Hp1bp3^C57BL/6N
• Name: heterochromatin protein 1, binding protein 3; C57BL/6N
• MGI ID: MGI:6472911
• Gene: Hp1bp3 Location: Chr4:137943607-137971994 bp, + strand Genetic Position: Chr4, 70.03 cM, cytoband D3
• Alliance: Hp1bp3^C57BL/6N page

Mutation origin

• Strain of Origin: C57BL/6N

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: A C>T mutation at chr4:138,221,673 (GRCm38) changes leucine codon16 to a phenylalanine codon (p.L16F). (J:296898)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any Hp1bp3 Mutation: 39 strains or lines available

References

• Original: J:296898 Tonelli Gombalova Z, et al., Majority of cerebrospinal fluid-contacting neurons in the spinal cord of C57Bl/6N mice is present in ectopic position unlike in other studied experimental mice strains and mammalian species. J Comp Neurol. 2020 Oct 15;528(15):2523-2550
• All: 1 reference(s)