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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Disp1
dispatched RND transporter family member 1
MGI:1916147
16 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Disp1icb/Disp1icb
Ptch1tm1Mps/Ptch1tm1Mps
involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J 		abnormal head morphology J:79027
abnormal neural tube morphology J:79027
embryonic lethality, complete penetrance J:79027
open neural tube J:79027
Disp1icb/Disp1icb
Shhtm1Amc/Shhtm5Amc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129/Sv * C57BL/6J * SWR 		abnormal frontonasal prominence morphology J:94270
perinatal lethality, complete penetrance J:94270
Disp1icb/Disp1tm1Amc
Shhtm1Amc/Shh+
involves: 129X1/SvJ * C57BL/6J 		abnormal neuron specification J:92058
failure of heart looping J:92058
holoprosencephaly J:92058
proboscis J:92058
Disp1tm1Amc/Disp1tm1Amc
Ptch1tm1Mps/Ptch1+
involves: 129S1/Sv * 129X1/SvJ 		normal nervous system phenotype J:92058
no abnormal phenotype detected J:92058
Disp1tm1Pab/Disp1tm1Pab
Shhtm2Chg/Shh+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA 		abnormal digit morphology J:109101
perinatal lethality, complete penetrance J:109101
preaxial polydactyly J:109101
Disp1tm2.1Amc/Disp1tm2.1Amc
Shhtm1Amc/Shh+
involves: 129/Sv * C57BL/6J * SWR 		abnormal neuron differentiation J:94270
absent floor plate J:94270
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
04/09/2024
MGI 6.23 		The Jackson Laboratory