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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cxcr4tm1Qma
targeted mutation 1, Qing Ma
MGI:1934166
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cxcr4tm1Qma/Cxcr4tm1Qma B6.129X-Cxcr4tm1Qma/J MGI:3617772
hm2
Cxcr4tm1Qma/Cxcr4tm1Qma involves: 129X1/SvJ MGI:2175786
hm3
Cxcr4tm1Qma/Cxcr4tm1Qma involves: 129X1/SvJ * C57BL/6 MGI:5317847
cx4
Cxcr4tm1Qma/Cxcr4tm1Qma
Gab1tm1Wbm/Gab1tm1Wbm
involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 MGI:3617774
cx5
Ccr5tm1Kuz/Ccr5tm1Kuz
Cxcr4tm1Qma/Cxcr4tm1Qma
involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 MGI:5317843


Genotype
MGI:3617772
hm1
Allelic
Composition
Cxcr4tm1Qma/Cxcr4tm1Qma
Genetic
Background
B6.129X-Cxcr4tm1Qma/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cxcr4tm1Qma mutation (1 available); any Cxcr4 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• at E10.75 fewer hypaxial muscle progenitor cells reach the floor of the first branchial arch
• at E10.75, fewer progenitor cells are seen in the dorsal limb and this reduction is more pronounced distally (35%) than proximally (25%)
• however, no significant change in proliferation of muscle progenitors is seen
• at E10.75, the number of muscle cells (MyoD+) is reduced in the dorsal limb and this reduction is more pronounced distally than proximally; however at E13.5 the size and distribution of the muscle groups is not significantly different from control
• increased apoptosis is seen in the proximal domain of the dorsal limb
• however, no significant difference is seen in the size of the tongue muscle

cellular
• at E10.75 fewer hypaxial muscle progenitor cells reach the floor of the first branchial arch
• at E10.75, fewer progenitor cells are seen in the dorsal limb and this reduction is more pronounced distally (35%) than proximally (25%)
• however, no significant change in proliferation of muscle progenitors is seen




Genotype
MGI:2175786
hm2
Allelic
Composition
Cxcr4tm1Qma/Cxcr4tm1Qma
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cxcr4tm1Qma mutation (1 available); any Cxcr4 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about 1/3 of mice are dead at E18.5

nervous system
• at E18.5, the cerebellum is disorganized with a highly distorted architecture and chromophillic cell clumps in the analage
• chromophillic clusters mostly contain early granule cell progenitors that are surrounded by Purkinje cells
• at E18.5, the external granule cell layer is attenuated and irregular

hematopoietic system
• at E18.5, the B220+/CD43+ pro-B cell population is severely reduced in the fetal liver (0.2% versus 7.0% in wild-type littermates); however T cell populations in the thymus are normal
• at E18.5 in the fetal liver, myeloid cells are reduced to 25% of wild-type, myelopoiesis is reduced and a marked erythroid predominance is seen
• at E18.5, a marked reduction in myeloid cells is also seen in the spleen and myeloid cells are virtually absent from the bone marrow
• at E15.5, bone marrow is hypocellular and composed mostly of stromal cells and osteoblasts with a severe reduction in hematopoiesis
• at E18.5, hematopoiesis is still reduced but cellularity is similar to wild-type; however myeloid cells are virtually absent

growth/size/body
• viable homozygotes are smaller than littermates

renal/urinary system
• prominent interstitial hemorrhage

respiratory system
• collapsed lungs

immune system
• at E18.5, the B220+/CD43+ pro-B cell population is severely reduced in the fetal liver (0.2% versus 7.0% in wild-type littermates); however T cell populations in the thymus are normal
• at E18.5 in the fetal liver, myeloid cells are reduced to 25% of wild-type, myelopoiesis is reduced and a marked erythroid predominance is seen
• at E18.5, a marked reduction in myeloid cells is also seen in the spleen and myeloid cells are virtually absent from the bone marrow

cardiovascular system
• prominent interstitial hemorrhage




Genotype
MGI:5317847
hm3
Allelic
Composition
Cxcr4tm1Qma/Cxcr4tm1Qma
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cxcr4tm1Qma mutation (1 available); any Cxcr4 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• abrogated neurotoxicity to gp120 from a CCR4 preferring isolate of HIV
• decreased survival from gp120 from a CCR5 preferring isolate of HIV

immune system
• decreased survival from gp120 from a CCR5 preferring isolate of HIV
• abrogated neurotoxicity to gp120 from a CCR5 preferring isolate of HIV

mortality/aging
• decreased survival from gp120 from a CCR5 preferring isolate of HIV




Genotype
MGI:3617774
cx4
Allelic
Composition
Cxcr4tm1Qma/Cxcr4tm1Qma
Gab1tm1Wbm/Gab1tm1Wbm
Genetic
Background
involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cxcr4tm1Qma mutation (1 available); any Cxcr4 mutation (40 available)
Gab1tm1Wbm mutation (0 available); any Gab1 mutation (78 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• at E10.75 and E11.5, no hypaxial muscle progenitor cells reach the floor of the first branchial arch
• only a fragment of the intrinsic muscle is present in the proximal tongue
• at E10.75, the number of muscle cells (MyoD+) is further reduced and the number of apoptotic cells is increased in the dorsal and ventral limbs compared to Gab single homozygotes
• limb muscle size is reduced and in the proximal portion of the lower forelimb, particular extensor muscles of dorsal limb are absent and the flexor muscles are reduced in size compared to Gab1 single homozygotes

digestive/alimentary system
• only a fragment of the intrinsic muscle is present in the proximal tongue
• the overall size of the tongue is very small

craniofacial
• only a fragment of the intrinsic muscle is present in the proximal tongue
• the overall size of the tongue is very small

cellular
• at E10.75 and E11.5, no hypaxial muscle progenitor cells reach the floor of the first branchial arch

growth/size/body
• only a fragment of the intrinsic muscle is present in the proximal tongue
• the overall size of the tongue is very small




Genotype
MGI:5317843
cx5
Allelic
Composition
Ccr5tm1Kuz/Ccr5tm1Kuz
Cxcr4tm1Qma/Cxcr4tm1Qma
Genetic
Background
involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ccr5tm1Kuz mutation (2 available); any Ccr5 mutation (29 available)
Cxcr4tm1Qma mutation (1 available); any Cxcr4 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• abrogated neurotoxicity to gp120 from a CCR5 preferring isolate of HIV
• abrogated neurotoxicity to gp120 from a CCR4 preferring isolate of HIV

immune system
• abrogated neurotoxicity to gp120 from a CCR5 preferring isolate of HIV
• abrogated neurotoxicity to gp120 from a CCR4 preferring isolate of HIV





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