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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Baiap2l1tm1.1Arte
targeted mutation 1.1, TaconicArtemis
MGI:6355370
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Baiap2l1tm1.1Arte/Baiap2l1tm1.1Arte involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac MGI:6359752
cx2
Baiap2Gt(XG757)Byg/Baiap2Gt(XG757)Byg
Baiap2l1tm1.1Arte/Baiap2l1tm1.1Arte
involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac MGI:6359753


Genotype
MGI:6359752
hm1
Allelic
Composition
Baiap2l1tm1.1Arte/Baiap2l1tm1.1Arte
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Baiap2l1tm1.1Arte mutation (0 available); any Baiap2l1 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
N
• homozygotes are overtly normal and show no developmental defects

embryo
N
• no placental defects are observed; labyrinth vascularization appears normal




Genotype
MGI:6359753
cx2
Allelic
Composition
Baiap2Gt(XG757)Byg/Baiap2Gt(XG757)Byg
Baiap2l1tm1.1Arte/Baiap2l1tm1.1Arte
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Baiap2Gt(XG757)Byg mutation (1 available); any Baiap2 mutation (29 available)
Baiap2l1tm1.1Arte mutation (0 available); any Baiap2l1 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• non-resorbed embryos are detected in only 1 out of 10 litters analyzed at E18.8
• no double homozygotes are recovered at weaning
• only 2.7% of double homozygotes are recovered at E18.5
• although double homozygotes are present at normal Mendelian ratios at E10.5, reduced numbers are detected at E14.5

integument
• at E14.5, almost all (14 of 15) double homozygotes show severe subcutaneous edema

cardiovascular system
N
• in vitro angiogenesis of E14.5 umbilical arterial explants in response to VEGF signals is normal
• at E14.5, vessel density of double homozygotes is only ~50% of wild-type and, more significantly, 30% less than that in single Baiap2Gt(XG757)Byg homozygotes
• average lumen size of CD31+ blood vessels is ~12.4% larger than that in single Baiap2Gt(XG757)Byg homozygotes
• at E14.5, double homozygotes exhibit early cardiac defects similar to those observed in single Baiap2Gt(XG757)Byg homozygotes
• at E10.5, double homozygotes display heart tube malformations
• at E14.5, double homozygotes show incomplete IVS closure
• at E14.5, double homozygotes show malformation of the mesenchymal membranous part of the septa
• at E14.5, the heart right ventricles are misshapen
• at E10.5, double homozygotes exhibit pericardial edema with similar ratios as single Baiap2Gt(XG757)Byg homozygotes

embryo
• at E14.5, vessel density of double homozygotes is only ~50% of wild-type and, more significantly, 30% less than that in single Baiap2Gt(XG757)Byg homozygotes
• average lumen size of CD31+ blood vessels is ~12.4% larger than that in single Baiap2Gt(XG757)Byg homozygotes
• at E14.5, patches of trophoblast giant cells are observed in the spongiotrophoblast layer
• at E14.5, placentas exhibit a much thinner and significantly more disorganized Tpbpa+ spongiotrophoblast layer than that in single Baiap2Gt(XG757)Byg homozygotes

homeostasis/metabolism
• at E10.5, double homozygotes exhibit pericardial edema with similar ratios as single Baiap2Gt(XG757)Byg homozygotes
• at E14.5, almost all (14 of 15) double homozygotes show severe subcutaneous edema

limbs/digits/tail
• at E14.5, almost all (13 of 15) double homozygotes show forepaw oligodactyly; loss of posterior digits in the right forepaw is observed





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory