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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Dhrs3
dehydrogenase/reductase 3
MGI:1315215
28 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Dhrs3tm1(NCOM)Mfgc/Dhrs3tm1(NCOM)Mfgc
involves: C57BL/6 * C57BL/6N
abnormal enzyme/coenzyme activity J:214109
abnormal retinol level J:214109
abnormal retinol metabolism J:214109
cleft palate J:214109
edema J:214109
eyelids open at birth J:214109
microphthalmia J:214109
perinatal lethality, complete penetrance J:214109
Dhrs3tm1Lex/Dhrs3+
involves: 129S5/SvEvBrd * C57BL/6J
enhanced sensorimotor gating J:171883
Dhrs3tm1Lex/Dhrs3tm1Lex
involves: 129S5/SvEvBrd * C57BL/6
abnormal axial skeleton morphology J:203823
abnormal craniofacial morphology J:203823
abnormal heart morphology J:203823
abnormal interventricular septum morphology J:203823
abnormal retinol metabolism J:203823
absent gastric milk in neonates J:203823
atrial septal defect J:203823
cervical vertebral fusion J:203823
decreased birth body size J:203823
delayed bone ossification J:203823
double outlet right ventricle J:203823
eyelids open at birth J:203823
failure of palatal shelf elevation J:203823
fetal growth retardation J:203823
micrognathia J:203823
neonatal lethality, complete penetrance J:203823
perinatal lethality, incomplete penetrance J:203823
ventricular septal defect J:203823
vertebral fusion J:203823
Dhrs3tm1Lex/Dhrs3tm1Lex
involves: 129S5/SvEvBrd * C57BL/6J
preweaning lethality, complete penetrance J:171883
Dhrs3tm1Lex/Dhrs3tm1Lex
Tg(RARE-Hspa1b/lacZ)12Jrt/0
involves: 129S5/SvEvBrd * C57BL/6 * CD-1
abnormal embryo development J:203823

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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
04/09/2024
MGI 6.23
The Jackson Laboratory