About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hoxb6tm1Mrc
targeted mutation 1, Mario R Capecchi
MGI:2151485
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hoxb6tm1Mrc/Hoxb6tm1Mrc involves: 129S7/SvEvBrd MGI:2673169
cx2
Hoxb5tm1Mrc/Hoxb5+
Hoxb6tm1Mrc/Hoxb6+
involves: 129S7/SvEvBrd MGI:3611769
cx3
Hoxa6tm1Mrc/Hoxa6tm1Mrc
Hoxb6tm1Mrc/Hoxb6tm1Mrc
Hoxc6tm1Dds/Hoxc6tm1Dds
involves: 129S7/SvEvBrd MGI:4358349
cx4
Hoxa5tm1Rob/Hoxa5+
Hoxa6tm1Mrc/Hoxa6+
Hoxb5tm1Mrc/Hoxb5+
Hoxb6tm1Mrc/Hoxb6+
Hoxc5tm1Mrc/Hoxc5+
Hoxc6tm1Dds/Hoxc6+
involves: 129S/SvEv * 129S7/SvEvBrd MGI:4358354


Genotype
MGI:2673169
hm1
Allelic
Composition
Hoxb6tm1Mrc/Hoxb6tm1Mrc
Genetic
Background
involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxb6tm1Mrc mutation (0 available); any Hoxb6 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• penetrance about 50%
• rarely, only the ventral portion of the first rib is present
• sometimes a gap exists between the dorsal and ventral portions of the first rib
• absence or shortening of first rib
• bifurcation of the second rib so that the upper branch articulates with the top of the sternum
• bifurcation occurs at the point bone-cartilage junction in newborns
• first detectable around E11.5
• altered lateral processes on T1
• T1 to C7 transformation the most prevalent vertebral abnormality
• C7 to C6 transformation
• tuberculum anterior of C6 either shifted to C7 (C6 to C5 transformation) or duplicated there

nervous system
• path of first intercostals nerve altered due to the abnormal rib structures




Genotype
MGI:3611769
cx2
Allelic
Composition
Hoxb5tm1Mrc/Hoxb5+
Hoxb6tm1Mrc/Hoxb6+
Genetic
Background
involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxb5tm1Mrc mutation (0 available); any Hoxb5 mutation (11 available)
Hoxb6tm1Mrc mutation (0 available); any Hoxb6 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• T1 to C7 transformation frequent
• C6 to C5 and/or C7 to C6 transformation in 52% of double heterozygotes
• occurs in the absence of T1 to C7 transformations




Genotype
MGI:4358349
cx3
Allelic
Composition
Hoxa6tm1Mrc/Hoxa6tm1Mrc
Hoxb6tm1Mrc/Hoxb6tm1Mrc
Hoxc6tm1Dds/Hoxc6tm1Dds
Genetic
Background
involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxa6tm1Mrc mutation (0 available); any Hoxa6 mutation (9 available)
Hoxb6tm1Mrc mutation (0 available); any Hoxb6 mutation (14 available)
Hoxc6tm1Dds mutation (0 available); any Hoxc6 mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• sternebra are poorly formed or missing
• reduced or absent
• rib projections extend from T2 through T6 with ribs from T2 through T4 exhibiting the same angle as T1 ribs
• mice are missing a complete first rib
• from T2 to T4
• mice exhibit anterior homeotic transformation from C6 to T6
• however, posterior thoracic, lumbar, and sacral vertebrae are normal in appearance and position
• T2 does not form a rib
• anterior projections do not begin until T4 and continue through T6 unlike in wild-type mice
• C7 exhibit a vertebral foramina unlike in wild-type mice




Genotype
MGI:4358354
cx4
Allelic
Composition
Hoxa5tm1Rob/Hoxa5+
Hoxa6tm1Mrc/Hoxa6+
Hoxb5tm1Mrc/Hoxb5+
Hoxb6tm1Mrc/Hoxb6+
Hoxc5tm1Mrc/Hoxc5+
Hoxc6tm1Dds/Hoxc6+
Genetic
Background
involves: 129S/SvEv * 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxa5tm1Rob mutation (1 available); any Hoxa5 mutation (28 available)
Hoxa6tm1Mrc mutation (0 available); any Hoxa6 mutation (9 available)
Hoxb5tm1Mrc mutation (0 available); any Hoxb5 mutation (11 available)
Hoxb6tm1Mrc mutation (0 available); any Hoxb6 mutation (14 available)
Hoxc5tm1Mrc mutation (0 available); any Hoxc5 mutation (12 available)
Hoxc6tm1Dds mutation (0 available); any Hoxc6 mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• primaxial and abaxial skeleton defects are less severe than in either triple homozygote





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory