About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Drosha
drosha, ribonuclease type III
MGI:1261425
68 phenotypes from 6 alleles in 8 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Droshatm1.1Vlcg/Droshatm1.1Vlcg
involves: 129S6/SvEvTac * C57BL/6NTac
no abnormal phenotype detected J:200671
Droshatm1.1Vlcg/Droshatm3Vlcg
Gt(ROSA)26Sortm3.1(cre/ERT2)Vlcg/Gt(ROSA)26Sor+
involves: 129S6/SvEvTac * C57BL/6NTac
decreased body size J:200671
normal mortality/aging J:200671
Droshatm1Ghan/Droshatm1Ghan
Tg(KRT5-rtTA)1Glk/0
Tg(tetO-cre)1Jaw/0
involves: 129 * C57BL/6 * FVB/N
abnormal hair follicle bulge morphology J:183487
decreased body size J:183487
Droshatm1Litt/Droshatm1.1Litt
Foxp3tm4(YFP/icre)Ayr/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
abnormal interferon-gamma secretion J:138683
abnormal interleukin-4 secretion J:138683
abnormal T cell activation J:138683
blood vessel inflammation J:138683
enlarged lymph nodes J:138683
enlarged spleen J:138683
increased CD8-positive, alpha-beta T cell number J:138683
increased leukocyte cell number J:138683
liver inflammation J:138683
lung inflammation J:138683
premature death J:138683
Droshatm1Litt/Droshatm1.1Litt
Foxp3tm4(YFP/icre)Ayr/Foxp3tm4(YFP/icre)Ayr
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
abnormal interferon-gamma secretion J:138683
abnormal interleukin-4 secretion J:138683
abnormal regulatory T cell morphology J:138683
abnormal T cell activation J:138683
blood vessel inflammation J:138683
enlarged lymph nodes J:138683
enlarged spleen J:138683
increased CD8-positive, alpha-beta T cell number J:138683
increased leukocyte cell number J:138683
liver inflammation J:138683
lung inflammation J:138683
premature death J:138683
Droshatm1Litt/Droshatm1.1Litt
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
involves: 129 * 129P2/OlaHsd * C57BL/6 * FVB/N
abnormal interferon-gamma secretion J:138683
Droshatm1Litt/Droshatm1.1Litt
Tg(Cd4-cre)1Cwi/0
involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N
abnormal immune system physiology J:138683
cachexia J:138683
decreased body fat mass J:138683
decreased CD8-positive, alpha-beta T cell number J:138683
decreased double-positive T cell number J:138683
decreased lymphocyte cell number J:138683
decreased regulatory T cell number J:138683
decreased skeletal muscle mass J:138683
decreased thymocyte number J:138683
normal immune system phenotype J:138683
increased activated T cell number J:138683
increased gamma-delta T cell number J:138683
increased granulocyte number J:138683
intestinal inflammation J:138683
liver inflammation J:138683
lung inflammation J:138683
premature death J:138683
Droshatm1Litt/Droshatm1Litt
Tg(KRT5-rtTA)1Glk/0
Tg(tetO-cre)1Jaw/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
abnormal coat/ hair morphology J:183487
abnormal hair cycle catagen phase J:183487
abnormal hair follicle inner root sheath morphology J:183487
abnormal hair follicle morphology J:183487
abnormal hair follicle regression J:183487
abnormal hair growth J:183487
abnormal hair shaft morphology J:183487
abnormal skin physiology J:183487
alopecia J:183487
decreased body size J:183487
dry skin J:183487
epidermal hyperplasia J:183487
hair follicle degeneration J:183487
increased apoptosis J:183487
normal integument phenotype J:183487
scaly skin J:183487
small hair follicles J:183487
waved hair J:183487
Droshatm1Litt/Droshatm1Litt
Tg(Six2-EGFP/cre)1Amc/0
involves: 129P2/OlaHsd * CD-1
abnormal kidney development J:321428
abnormal kidney morphology J:321428
abnormal nephrogenic zone morphology J:321428
abnormal renal glomerulus morphology J:321428
absent kidney J:321428
congestive heart failure J:321428
cyanosis J:321428
decreased food intake J:321428
decreased locomotor activity J:321428
decreased renal glomerulus number J:321428
dilated renal tubule J:321428
increased kidney apoptosis J:321428
perinatal lethality, complete penetrance J:321428
polycystic kidney J:321428
pulmonary edema J:321428
renal hypoplasia J:321428
respiratory distress J:321428
Droshatm1Litt/Droshatm1Litt
Wt1tm2(cre/ERT2)Wtp/Wt1+
involves: 129P2/OlaHsd * 129S4/SvJae
increased urine protein level J:321428
normal mortality/aging J:321428
normal neoplasm J:321428
normal renal/urinary system phenotype J:321428
Droshatm2.1Vlcg/Droshatm2.1Vlcg
involves: 129S6/SvEvTac * C57BL/6NTac
no abnormal phenotype detected J:200671
Droshatm2.1Vlcg/Droshatm3Vlcg
Tg(Nanog-cre)#Vlcg/0
involves: 129S6/SvEvTac * C57BL/6NTac
embryonic lethality, complete penetrance J:200671
Droshatm3Vlcg/Droshatm3Vlcg
involves: 129S6/SvEvTac * C57BL/6NTac
embryonic lethality, complete penetrance J:200671

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