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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nubp2
nucleotide binding protein 2
MGI:1347072
25 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Nubp2dor/Nubp2dor
involves: C57BL/6J * FVB/NTac
abnormal brain morphology J:284772
abnormal digit development J:284772
abnormal eye development J:284772
abnormal first pharyngeal arch morphology J:284772
abnormal lateral nasal prominence morphology J:284772
abnormal medial nasal prominence morphology J:284772
abnormal midface morphology J:284772
absent mandible J:284772
absent maxillary prominence J:284772
absent snout J:284772
embryonic growth retardation J:284772
encephalomeningocele J:284772
fetal growth retardation J:284772
hematoma J:284772
lethality during fetal growth through weaning, incomplete penetrance J:284772
micromelia J:284772
midline facial cleft J:284772
oligodactyly J:284772
protruding tongue J:284772
small frontonasal prominence J:284772
small mandibular prominence J:284772
small maxillary prominence J:284772
Nubp2tm1b(EUCOMM)Hmgu/Nubp2+
C57BL/6N-Nubp2tm1b(EUCOMM)Hmgu/Ieg
increased circulating fructosamine level J:211773
short tibia J:211773
Nubp2tm1b(EUCOMM)Hmgu/Nubp2tm1b(EUCOMM)Hmgu
C57BL/6N-Nubp2tm1b(EUCOMM)Hmgu/Ieg
preweaning lethality, complete penetrance J:211773

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
12/10/2024
MGI 6.24
The Jackson Laboratory