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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Del(16Es2el-Sept5)3Bld
deletion, Chr 16, Antonio Baldini 3
MGI:3640126
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
 		Del(16Es2el-Sept5)3Bld/+ B6.Cg-Tyrc-Brd Del(16Es2el-Sept5)3Bld MGI:3640305
ht2
 		Del(16Es2el-Sept5)3Bld/+ involves: 129S7/SvEvBrd MGI:3713482
cx3
 		Del(16Es2el-Sept5)3Bld/+
Del(16Es2el-Ufd1l)217Bld/+ 		involves: 129S7/SvEvBrd MGI:3713489


Genotype
MGI:3640305
ht1
Allelic
Composition		 Del(16Es2el-Sept5)3Bld/+
Genetic
Background		 B6.Cg-Tyrc-Brd Del(16Es2el-Sept5)3Bld
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(16Es2el-Sept5)3Bld mutation (1 available); any Del(16Es2el-Sept5)3Bld mutation (1 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
nervous system
decreased prepulse inhibition ( J:110101 )
• PPI is significantly impaired; mice have reduced PPI




Genotype
MGI:3713482
ht2
Allelic
Composition		 Del(16Es2el-Sept5)3Bld/+
Genetic
Background		 involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(16Es2el-Sept5)3Bld mutation (1 available); any Del(16Es2el-Sept5)3Bld mutation (1 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
cardiovascular system
abnormal fourth pharyngeal arch artery morphology ( J:67409 )
• abnormal in all embryos at E10.5

craniofacial
abnormal fourth pharyngeal arch artery morphology ( J:67409 )
• abnormal in all embryos at E10.5

embryo
abnormal fourth pharyngeal arch artery morphology ( J:67409 )
• abnormal in all embryos at E10.5




Genotype
MGI:3713489
cx3
Allelic
Composition		 Del(16Es2el-Sept5)3Bld/+
Del(16Es2el-Ufd1l)217Bld/+
Genetic
Background		 involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(16Es2el-Sept5)3Bld mutation (1 available); any Del(16Es2el-Sept5)3Bld mutation (1 available)
Del(16Es2el-Ufd1l)217Bld mutation (1 available); any Del(16Es2el-Ufd1l)217Bld mutation (1 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
cardiovascular system
cardiovascular system phenotype ( J:67409 )
N
• no cardiovascular defects similar to those in other deletions are observed




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)
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Send questions and comments to User Support. 		last database update
05/07/2024
MGI 6.23 		The Jackson Laboratory