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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 (12 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 (27 available)
Hoxa6tm1Mrc mutation (0 available); any Hoxa6 mutation (9 available)
Hoxb5tm1Mrc mutation (0 available); any Hoxb5 mutation (12 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





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory