About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Disp1
dispatched RND transporter family member 1
MGI:1916147
64 phenotypes from 6 alleles in 6 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Disp1icb/Disp1icb
involves: 129/Sv * C57BL/6J * SWR 		abnormal brain development J:94270
abnormal facial morphology J:94270
abnormal heart development J:94270
abnormal limb morphology J:94270
abnormal somite development J:94270
abnormal vascular development J:94270
embryonic lethality, complete penetrance J:94270
Disp1icb/Disp1icb
involves: C3HeB/FeJ * C57BL/6J 		abnormal direction of embryo turning J:79027
abnormal forelimb morphology J:79027
abnormal head shape J:79027
abnormal left-right axis patterning J:98216
abnormal neural tube morphology J:79027
abnormal spinal cord morphology J:98216
embryonic lethality during organogenesis, complete penetrance J:79027, J:98216
failure of heart looping J:79027
normal nervous system phenotype J:79027
pericardial edema J:79027
Disp1icb/Disp1tm1Amc
involves: 129X1/SvJ * C57BL/6J 		abnormal basisphenoid bone morphology J:92058
abnormal craniofacial bone morphology J:92058
abnormal frontal bone morphology J:92058
abnormal head morphology J:92058
abnormal nasopharynx morphology J:92058
abnormal neurocranium morphology J:92058
abnormal occipital bone morphology J:92058
abnormal viscerocranium morphology J:92058
absent basisphenoid bone J:92058
absent occipital bone J:92058
absent parietal bone J:92058
absent pituitary gland J:92058
absent primary palate J:92058
absent upper incisors J:92058
absent vomeronasal organ J:92058
delayed chondrocyte differentiation J:92058
holoprosencephaly J:92058
Disp1icb/Disp1tm1Amc
Shhtm1(EGFP/cre)Cjt/Shh+
involves: 129X1/SvJ * C57BL/6J 		oligodactyly J:92504
Disp1icb/Disp1tm2Amc
Shhtm1(EGFP/cre)Cjt/Shh+
involves: 129/Sv * C57BL/6J * SWR 		abnormal facial morphology J:94270
abnormal nasal pit morphology J:94270
abnormal neuron differentiation J:94270
absent floor plate J:94270
absent parietal bone J:94270
absent premaxilla J:94270
neonatal lethality J:94270
Disp1tm1Amc/Disp1tm1Amc
involves: 129X1/SvJ 		abnormal craniofacial bone morphology J:92058
abnormal facial morphology J:92058
abnormal nasopharynx morphology J:92058
abnormal neuron specification J:92058
abnormal vomeronasal organ morphology J:92058
absent primary palate J:92058
absent upper incisors J:92058
holoprosencephaly J:92058
neonatal lethality, complete penetrance J:92058
ocular hypotelorism J:92058
philtrum hypoplasia J:92058
pituitary gland hypoplasia J:92058
respiratory distress J:92058
Disp1tm1Pab/Disp1tm1Pab
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal embryo turning J:79457
abnormal first pharyngeal arch morphology J:79457
abnormal heart looping J:79457
abnormal left-right axis patterning J:79457
abnormal neural fold formation J:79457
abnormal neural plate morphology J:79457
abnormal neural tube morphology J:79457
abnormal optic vesicle formation J:79457
abnormal somite development J:79457
decreased embryo size J:79457
distended pericardium J:79457
embryonic lethality during organogenesis, complete penetrance J:79457
fused first pharyngeal arch J:79457
Disp1tm1Ptch/Disp1tm1Ptch
involves: 129P2/OlaHsd 		abnormal dermomyotome development J:79831
abnormal forebrain morphology J:79831
abnormal heart development J:79831
abnormal left-right axis symmetry of the somites J:79831
abnormal neural tube morphology J:79831
abnormal sclerotome morphology J:79831
absent floor plate J:79831
cyclopia J:79831
distended pericardium J:79831
embryonic lethality during organogenesis, complete penetrance J:79831
failure of heart looping J:79831
holoprosencephaly J:79831
incomplete embryo turning J:79831
Disp1tm2.1Amc/Disp1tm2Amc
Shhtm1(EGFP/cre)Cjt/Shh+
involves: 129/Sv * C57BL/6J * SWR 		abnormal facial morphology J:94270
abnormal nasal pit morphology J:94270
abnormal neuron differentiation J:94270
abnormal parietal bone morphology J:94270
absent premaxilla J:94270
neonatal lethality J:94270
Disp1tm2Amc/Disp1tm2Amc
involves: 129/Sv * C57BL/6J * SWR 		no abnormal phenotype detected 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)
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