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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nubp2tm1c(EUCOMM)Hmgu
targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH
MGI:6450511
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Nubp2tm1c(EUCOMM)Hmgu/Nubp2tm1c(EUCOMM)Hmgu
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(Wnt1-GAL4)11Rth/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/J MGI:6452819
cn2
Nubp2tm1c(EUCOMM)Hmgu/Nubp2tm1c(EUCOMM)Hmgu
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(Wnt1-GAL4)11Rth/0
involves: C57BL/6 MGI:6450919


Genotype
MGI:6452819
cn1
Allelic
Composition
Nubp2tm1c(EUCOMM)Hmgu/Nubp2tm1c(EUCOMM)Hmgu
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(Wnt1-GAL4)11Rth/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo mutation (10 available); any Gt(ROSA)26Sor mutation (993 available)
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
Nubp2tm1c(EUCOMM)Hmgu mutation (0 available); any Nubp2 mutation (17 available)
Tg(Wnt1-GAL4)11Rth mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• reduced +GFP craniofacial neural crest cells in nasal prominences and pharyngeal arches due to increased apoptosis between E9.5 and E10.5

cellular
• reduced +GFP craniofacial neural crest cells in nasal prominences and pharyngeal arches due to increased apoptosis between E9.5 and E10.5




Genotype
MGI:6450919
cn2
Allelic
Composition
Nubp2tm1c(EUCOMM)Hmgu/Nubp2tm1c(EUCOMM)Hmgu
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(Wnt1-GAL4)11Rth/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
Nubp2tm1c(EUCOMM)Hmgu mutation (0 available); any Nubp2 mutation (17 available)
Tg(Wnt1-GAL4)11Rth mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• undersized facial primordia at E10.5
• olfactory epithelium is continuous with the oral cavity

growth/size/body
• undersized facial primordia at E10.5
• olfactory epithelium is continuous with the oral cavity
• craniofacial mesenchyme exhibit a slight increase in average cilia per cell compared with control mice
• however, there is no difference in centriole number

embryo
• craniofacial mesenchyme exhibit a slight increase in average cilia per cell compared with control mice
• however, there is no difference in centriole number

digestive/alimentary system
• olfactory epithelium is continuous with the oral cavity

nervous system
• brain is shifted rostrally

respiratory system
• olfactory epithelium is continuous with the oral cavity

skeleton

taste/olfaction
• olfactory epithelium is continuous with the oral cavity





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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory