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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Derl2
Der1-like domain family, member 2
MGI:2151483
21 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cd19tm1(cre)Cgn/Cd19+
Derl2tm1.1Hpl/Derl2tm1.1Hpl
involves: 129P2/OlaHsd
normal immune system phenotype J:170650
Derl2tm1.1Hpl/Derl2tm1.1Hpl
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: C57BL/6 * DBA
normal liver/biliary system phenotype J:170650
Derl2tm1.2Hpl/Derl2tm1.2Hpl
involves: BALB/cJ
abnormal axial skeleton morphology J:170650
abnormal cell physiology J:170650
abnormal chondrocyte morphology J:170650
abnormal chondrocyte physiology J:170650
abnormal lung volume J:170650
abnormal rib morphology J:170650
abnormal thoracic cage shape J:170650
absent gastric milk in neonates J:170650
cachexia J:170650
decreased body weight J:170650
hypoglycemia J:170650
lethality, incomplete penetrance J:170650
male infertility J:170650
neonatal lethality, incomplete penetrance J:170650
pregnancy-related premature death J:170650
premature death J:170650
respiratory distress J:170650
sternebra fusion J:170650
Derl2tm1b(EUCOMM)Hmgu/Derl2tm1b(EUCOMM)Hmgu
C57BL/6N-Derl2tm1b(EUCOMM)Hmgu/Ics
preweaning lethality, complete penetrance J:211773

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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
11/12/2024
MGI 6.24
The Jackson Laboratory