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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Phox2b
paired-like homeobox 2b
MGI:1100882
14 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Kcnk5Gt(KST024)Byg/Kcnk5+
Phox2btm2Jbr/Phox2b+
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 		abnormal retrotrapezoid nucleus morphology J:157526
Nkx6-2tm1Ercs/Nkx6-2+
Phox2btm1(Phox2a)Mist/Phox2b+
involves: 129P2/OlaHsd * 129S4/SvJae 		abnormal axon extension J:126634
abnormal vagus ganglion morphology J:126634
Pcgf1tm1.1Hko/Pcgf1tm1.1Hko
Phox2bem3(cre)Heno/Phox2b+
involves: 129 * C57BL/6 * C57BL/6N * DBA 		abnormal colon morphology J:344865
abnormal feces composition J:344865
abnormal ileum morphology J:344865
abnormal intestinal transit time J:344865
abnormal jejunum morphology J:344865
decreased body size J:344865
decreased feces water content J:344865
decreased neuron number J:344865
decreased survivor rate J:344865
increased neuron number J:344865
postnatal growth retardation J:344865
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
11/12/2024
MGI 6.24 		The Jackson Laboratory