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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ednrb
endothelin receptor type B
MGI:102720
59 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Ay/a
Ednrbs/Ednrbs
Not Specified
variable body spotting J:12954
Ednratm1Ywa/Ednratm1Ywa
Ednrbtm1Ywa/Ednrbtm1Ywa
involves: 129S7/SvEvBrd
abnormal artery morphology J:46640
pericardial effusion J:46640
prenatal lethality J:46640
Ednrbs-3CHLo/Ednrbs-3CHLo
involves: 101/Rl * C3H/Rl
megacolon J:44601, J:100221
postnatal lethality, complete penetrance J:44601, J:100221
white spotting J:44601, J:100221
Ednrbs-15DttMb/Ednrb+
Mycbp2tm1.1Adia/Mycbp2+
involves: 101/Rl * C3H/Rl * C57BL/6 * FVB/N
abnormal nervous system morphology J:125702
Ednrbs-24Pub/Ednrb+
Mycbp2m274-4Tpo/Mycbp2+
involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ
neonatal lethality, complete penetrance J:149893
respiratory distress J:149893
Ednrbs-24Pub/Ednrb+
m128-7Tpo/m128-7Tpo+
involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ
abnormal direction of heart looping J:149893
abnormal head morphology J:149893
abnormal pharyngeal arch morphology J:149893
abnormal vitelline vasculature morphology J:149893
embryonic lethality, complete penetrance J:149893
enlarged pericardium J:149893
hemopericardium J:149893
incomplete embryo turning J:149893
Ednrbs-24Pub/Ednrb+
m174-16Tpo/m174-16Tpo+
involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ
lethality throughout fetal growth and development, complete penetrance J:149893
Ednrbs-24Pub/Ednrb+
m183-15Tpo/m183-15Tpo+
involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ
embryonic lethality between implantation and somite formation, complete penetrance J:149893
Ednrbs-24Pub/Ednrb+
m251-2Tpo/m251-2Tpo+
involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ
preweaning lethality, complete penetrance J:149893
Ednrbs-24Pub/Ednrb+
m283-1Tpo/m283-1Tpo+
involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ
preweaning lethality, complete penetrance J:149893
Ednrbs-24Pub/Ednrbs-24Pub
m289-5Tpo/m289-5Tpo+
involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ
preweaning lethality, complete penetrance J:149893
Ednrbs-31Pub/Ednrb+
involves: 101/Rl * C3H/Rl
decreased body size J:100221
Ednrbs-31Pub/Ednrbs-31Pub
involves: 101/Rl * C3H/Rl
prenatal lethality, complete penetrance J:100221
Ednrbs-36Pub/Ednrb+
Spry2tm1.1Mrt/Spry2+
involves: 101/Rl * 129P2/OlaHsd * C3H/Rl * C57BL/6J
abnormal palatal rugae morphology J:125229
cleft secondary palate J:125229
Ednrbs-36Pub/Ednrbs-36Pub
Tg(Spry2)2Tpo/0
B6.Cg-Ednrbs-36Pub Tg(Spry2)2Tpo
abnormal palate bone morphology J:125229
cleft secondary palate J:125229
normal craniofacial phenotype J:125229
maxillary shelf hypoplasia J:125229
Ednrbs-36Pub/Ednrbs-36Pub
Tg(Spry2)69Tpo/0
B6.Cg-Ednrbs-36Pub Tg(Spry2)69Tpo
abnormal palate bone morphology J:125229
cleft secondary palate J:125229
normal craniofacial phenotype J:125229
maxillary shelf hypoplasia J:125229
Ednrbs/Ednrbs-3CHLo
involves: 101/Rl * C3H/Rl
white spotting J:100221
Ednrbs/Ednrbs-31Pub
involves: 101/Rl * C3H/Rl
decreased body size J:100221
white spotting J:100221
Ednrbs/Ednrbs
Lystbg-slt/Lystbg-slt
involves: C57BL/10Ch * Y257/Ch
abnormal eye pigmentation J:25388
Ednrbs/Ednrbs
Mc1re/Mc1re
Not Specified
white spotting J:5110
yellow coat color J:5110
Ednrbtm1.1Nat/Ednrbtm1.2Nat
Igs1tm11(CAG-Bgeo,-Edn2)Nat/Igs1+
Tg(Pax6-cre,GFP)2Pgr/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal retina vasculature morphology J:201133
Ednrbtm1Nrd/Ednrbtm1Nrd
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/J
abnormal enteric neural crest cell migration J:140320
aganglionic megacolon J:140320
distended abdomen J:140320
premature death J:140320
slow postnatal weight gain J:140320
white spotting J:140320
Ednrbtm1Nrd/Ednrbtm1Nrd
Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * CBA/J
abnormal mature B cell number J:233811
abnormal Peyer's patch morphology J:233811
abnormal spleen morphology J:233811
abnormal splenic cell ratio J:233811
decreased B cell number J:233811
decreased germinal center B cell number J:233811
decreased IgA level J:233811
decreased marginal zone B cell number J:233811
decreased spleen red pulp amount J:233811
decreased spleen weight J:233811
decreased spleen white pulp amount J:233811
large intestinal inflammation J:233811
small Peyer's patches J:233811
small spleen J:233811
Ednrbtm1Nrd/Ednrbtm1Nrd
Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
Tg(Tyr-cre/ERT2)13Bos/0
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J
abnormal coat/hair pigmentation J:231435
abnormal hair follicle melanocyte morphology J:231435
abnormal melanocyte proliferation J:231435
absent hair follicle melanin granules J:231435
decreased melanocyte number J:231435
reduced hair shaft melanin granule number J:231435
Ednrbtm1Ywa/Ednrb+
Tg(Mt1-RET)304Ina/0
involves: 129S7/SvEvBrd * BALB/c * C57BL/6
decreased tumor-free survival time J:155735
increased melanoma incidence J:155735
increased metastatic potential J:155735

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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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory