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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hoxa4tm1Bhr
targeted mutation 1, Richard R Behringer
MGI:1857628
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hoxa4tm1Bhr/Hoxa4tm1Bhr either: 129S/SvEv-Hoxa4tm1Bhr or (involves: 129S7/SvEvBrd * C57BL/6) MGI:2167813
ht2
Hoxa4tm1Bhr/Hoxa4+ 129S/SvEv-Hoxa4tm1Bhr MGI:3611207
ht3
Hoxa4tm1Bhr/Hoxa4+ involves: 129S7/SvEvBrd * C57BL/6 MGI:3611203
cx4
Hoxa4tm1Bhr/Hoxa4tm1Bhr
Hoxb4tm1Bay/Hoxb4tm1Bay
involves: 129S7/SvEvBrd * C57BL/6 MGI:3611204
cx5
Hoxa4tm1Bhr/Hoxa4tm1Bhr
Hoxb4tm1Bay/Hoxb4tm1Bay
Hoxd4tm1Bhr/Hoxd4tm1Bhr
involves: 129S/SvEv MGI:3611055
cx6
Hoxa4tm1Bhr/Hoxa4tm1Bhr
Hoxd4tm1Bhr/Hoxd4tm1Bhr
involves: 129S/SvEv MGI:3611052


Genotype
MGI:2167813
hm1
Allelic
Composition
Hoxa4tm1Bhr/Hoxa4tm1Bhr
Genetic
Background
either: 129S/SvEv-Hoxa4tm1Bhr or (involves: 129S7/SvEvBrd * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxa4tm1Bhr mutation (0 available); any Hoxa4 mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Homeotic transformation of C3 in Hoxa4tm1Bhr/Hoxa4tm1Bhr mice

skeleton
• 33% with 1-2 fused sternebrae
• 48% develop an extensive rib on the 7th cervical vertebra (C7), of these 20% are long enough to fuse to the costal cartilage of the T1 rib
• extensive ribs on C7 in 48% of homozygotes
• processus spinus normally associated with C2 is also found on C3 in 71% of homozygotes
• rarely, asymetrical ossification




Genotype
MGI:3611207
ht2
Allelic
Composition
Hoxa4tm1Bhr/Hoxa4+
Genetic
Background
129S/SvEv-Hoxa4tm1Bhr
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxa4tm1Bhr mutation (0 available); any Hoxa4 mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• Background Sensitivity: C7 ribs are less common
• Background Sensitivity: C7 ribs are less common




Genotype
MGI:3611203
ht3
Allelic
Composition
Hoxa4tm1Bhr/Hoxa4+
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxa4tm1Bhr mutation (0 available); any Hoxa4 mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• Background Sensitivity: C7 ribs in 19% of heterozygotes
• Background Sensitivity: C7 ribs in 19% of heterozygotes




Genotype
MGI:3611204
cx4
Allelic
Composition
Hoxa4tm1Bhr/Hoxa4tm1Bhr
Hoxb4tm1Bay/Hoxb4tm1Bay
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxa4tm1Bhr mutation (0 available); any Hoxa4 mutation (9 available)
Hoxb4tm1Bay mutation (1 available); any Hoxb4 mutation (20 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• died within the first week of life

skeleton
• loss of lateral articulations between C2 and C3
• large processus spinosi on both C2 and C3
• C7 rib found in Hoxa4tm1Bhr single homozygotes is not found
• anterior tuberculi shifted from C6 to C7
• fusions of C2 and C3




Genotype
MGI:3611055
cx5
Allelic
Composition
Hoxa4tm1Bhr/Hoxa4tm1Bhr
Hoxb4tm1Bay/Hoxb4tm1Bay
Hoxd4tm1Bhr/Hoxd4tm1Bhr
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxa4tm1Bhr mutation (0 available); any Hoxa4 mutation (9 available)
Hoxb4tm1Bay mutation (1 available); any Hoxb4 mutation (20 available)
Hoxd4tm1Bhr mutation (0 available); any Hoxd4 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• atlas like anterior arches on C1 through C5
• lateral foramina on C2, C3, and C4
• C6 to C5 and C7 to C6 transformations




Genotype
MGI:3611052
cx6
Allelic
Composition
Hoxa4tm1Bhr/Hoxa4tm1Bhr
Hoxd4tm1Bhr/Hoxd4tm1Bhr
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hoxa4tm1Bhr mutation (0 available); any Hoxa4 mutation (9 available)
Hoxd4tm1Bhr mutation (0 available); any Hoxd4 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• dorsal cartilage between C2 and C3 fuses, penetrance 17%
• lateral ossified portions of C2 and C3 never fuse
• C7 ribs
• large processus spinosi on both C2 and C3





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last database update
10/09/2024
MGI 6.24
The Jackson Laboratory