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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Zeb2
zinc finger E-box binding homeobox 2
MGI:1344407
28 phenotypes from 3 alleles in 10 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Gt(ROSA)26Sortm18(Zeb2)Jhai/Gt(ROSA)26Sortm18(Zeb2)Jhai
Tg(Cd4-cre)1Cwi/0
involves: C57BL/6 * CD-1 * DBA/2
increased T cell acute lymphoblastic leukemia incidence J:263520
premature death J:263520
Gt(ROSA)26Sortm18(Zeb2)Jhai/Gt(ROSA)26Sortm18(Zeb2)Jhai
Tg(Tek-cre)1Ywa/0
involves: C57BL/6 * CD-1 * SJL
increased T cell acute lymphoblastic leukemia incidence J:263520
increased thymus tumor incidence J:263520
premature death J:263520
Zeb2tm1.1Yhi/Zeb2tm1.1Yhi
Tg(Dct-lacZ)A12Jkn/0
Tg(Tyr-cre)1Lru/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2
abnormal hair follicle bulge morphology J:211299
abnormal hair follicle melanocyte morphology J:211299
abnormal melanoblast migration J:211299
abnormal melanoblast morphology J:211299
abnormal melanosome morphology J:211299
absent hair follicle melanin granules J:211299
reduced hair shaft melanin granule number J:211299
Zeb2tm1.1Yhi/Zeb2tm1.1Yhi
Tg(Pax6-cre)1Knd/0
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
abnormal lens fiber morphology J:101730
abnormal lens morphology J:101730
small lens J:101730
Zeb2tm1.1Yhi/Zeb2tm1.1Yhi
Tg(Pax6-cre,GFP)1Pgr/0
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * FVB
abnormal lens fiber morphology J:101730
abnormal lens morphology J:101730
small lens J:101730
Zeb2tm1.1Yhi/Zeb2tm1.1Yhi
Tg(Tyr-cre)1Lru/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2
hypopigmentation J:211299
reduced hair shaft melanin granule number J:211299
Zeb2tm1.2Yhi/Zeb2+
involves: 129S1/Sv * 129X1/SvJ * CD-1
normal nervous system phenotype J:82084
Zeb2tm1.2Yhi/Zeb2tm1.2Yhi
involves: 129S1/Sv * 129X1/SvJ
embryonic lethality during organogenesis, complete penetrance J:75138
Zeb2tm1.2Yhi/Zeb2tm1.2Yhi
involves: 129S1/Sv * 129X1/SvJ * CD-1
abnormal cranial neural crest cell migration J:82084
abnormal neural crest cell delamination J:82084
abnormal neural plate morphology J:82084
absent first pharyngeal arch J:82084
absent vagal neural crest cells J:82084
embryonic growth arrest J:82084
embryonic lethality during organogenesis, complete penetrance J:82084
incomplete embryo turning J:82084
open neural tube J:82084
Zeb2tm1.2Yhi/Zeb2tm1.2Yhi
involves: 129S1/Sv * 129X1/SvJ * FVB/N
abnormal embryo development J:75138
embryonic lethality during organogenesis, complete penetrance J:75138
Zeb2tm1.2Yhi/Zeb2tm1.2Yhi
involves: 129S1/Sv * 129X1/SvJ * ICR
abnormal neural plate morphology J:108819
abnormal somite development J:101031, J:108819
abnormal somite shape J:101031
decreased somite size J:101031, J:108819
open neural tube J:108819

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
04/16/2024
MGI 6.23
The Jackson Laboratory