About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nfkb2
nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100
MGI:1099800
41 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Nfkb1tm1Bal/Nfkb1tm1Bal
Nfkb2tm1Sbn/Nfkb2tm1Sbn
involves: 129P2/OlaHsd * 129S4/SvJae
abnormal bone marrow cavity morphology J:45119
abnormal immune system organ morphology J:45119
abnormal long bone morphology J:45119
abnormal macrophage physiology J:45119
abnormal osteoclast differentiation J:45119
abnormal spleen morphology J:45119
abnormal thymus cortex morphology J:45119
abnormal thymus medulla morphology J:45119
absent lymph nodes J:45119
absent spleen white pulp J:45119
arrested B cell differentiation J:45119
decreased B cell number J:45119
decreased CD4-positive, alpha-beta T cell number J:45119
decreased CD8-positive, alpha-beta T cell number J:45119
decreased dendritic cell number J:45119
decreased double-positive T cell number J:45119
decreased length of long bones J:45119
decreased mature B cell number J:45119
decreased osteoclast cell number J:45119
decreased single-positive T cell number J:45119
decreased T cell number J:45119
failure of tooth eruption J:45119
increased granulocyte number J:45119
increased macrophage cell number J:45119
osteopetrosis J:45119
postnatal growth retardation J:45119
premature death J:45119
thymus hypoplasia J:45119
Nfkb1tm1Brv/Nfkb1tm1Brv
Nfkb2tm1Brv/Nfkb2+
involves: 129S1/Sv * C57BL/6
abnormal bone structure J:44112
abnormal osteoclast differentiation J:44112
decreased osteoclast cell number J:44112
Nfkb1tm1Brv/Nfkb1tm1Brv
Nfkb2tm1Brv/Nfkb2tm1Brv
involves: 129S1/Sv * C57BL/6
abnormal bone marrow cavity morphology J:44112
abnormal craniofacial morphology J:44112
abnormal cytokine secretion J:44112
abnormal long bone epiphyseal plate morphology J:44112
abnormal long bone morphology J:44112
abnormal osteoclast differentiation J:44112
decreased interleukin-6 secretion J:44112
decreased osteoclast cell number J:44112
increased macrophage cell number J:44112
osteopetrosis J:44112
postnatal growth retardation J:44112
tooth impaction J:44112
Nfkb2Lym1/Nfkb2+
Otub1tm1c(EUCOMM)Hmgu/Otub1tm1c(EUCOMM)Hmgu
Cd19tm1(cre)Cgn/Cd19+
involves: 129P2/OlaHsd * BALB/c * C57BL/6 * C57BL/6N
normal immune system phenotype J:280549
Nfkb2tm2Brv/Nfkb2+
Traf3tm1Bal/Traf3tm1Bal
involves: 129S1/Sv * 129S4/SvJae * C57BL/6
postnatal lethality, complete penetrance J:124635
Nfkb2tm2Brv/Nfkb2tm2Brv
Tg(Tnfsf13b)1Fma/?
B6.Cg-Nfkb2tm2Brv Tg(Tnfsf13b)1Fma
abnormal B cell activation J:113556
absent spleen marginal zone J:113556
decreased marginal zone B cell number J:113556
normal immune system phenotype J:113556
increased urine protein level J:113556
Nfkb2tm2Brv/Nfkb2tm2Brv
Traf3tm1Bal/Traf3tm1Bal
involves: 129S1/Sv * 129S4/SvJae * C57BL/6
normal immune system phenotype J:124635
normal mortality/aging J:124635

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory