About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Tgfbr3
transforming growth factor, beta receptor III
MGI:104637
42 phenotypes from 3 alleles in 4 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Tgfbr3em1(IMPC)Mbp/Tgfbr3+
C57BL/6N-Tgfbr3em1(IMPC)Mbp/MbpMmucd 		abnormal blood vessel morphology J:211773
abnormal kidney morphology J:211773
abnormal placenta morphology J:211773
abnormal placenta vasculature J:211773
enlarged kidney J:211773
microphthalmia J:211773
Tgfbr3em1(IMPC)Mbp/Tgfbr3em1(IMPC)Mbp
C57BL/6N-Tgfbr3em1(IMPC)Mbp/MbpMmucd 		abnormal blood vessel morphology J:211773
abnormal placenta morphology J:211773
abnormal placenta vasculature J:211773
edema J:211773
embryonic growth retardation J:211773
hemorrhage J:211773
pale liver J:211773
preweaning lethality, complete penetrance J:211773
Tgfbr3tm1.1Jba/Tgfbr3tm1.1Jba
involves: 129S6/SvEvTac 		abnormal palatal shelf bone ossification J:218259
abnormal palatal shelf fusion at midline J:218259
abnormal palate development J:218259
abnormal vasculogenesis J:218259
decreased palatal shelf size J:218259
decreased tongue size J:218259
failure of palatal shelf elevation J:218259
lethality throughout fetal growth and development, complete penetrance J:218259
Tgfbr3tm1.1Jba/Tgfbr3tm1.1Jba
involves: 129S6/SvEvTac * C57BL/6 		abnormal epicardium morphology J:141344
abnormal truncus arteriosus septation J:141344
abnormal vasculogenesis J:141344
lethality throughout fetal growth and development, complete penetrance J:141344
thin myocardium J:141344
transposition of great arteries J:141344
Tgfbr3tm1Stv/Tgfbr3tm1Stv
involves: 129/Sv * C57BL/6 		abnormal axial skeleton morphology J:83727
abnormal definitive hematopoiesis J:83727
abnormal femur morphology J:83727
abnormal fertility/fecundity J:83727
abnormal fetal cardiomyocyte proliferation J:83727
abnormal interventricular septum muscular part morphology J:83727
abnormal liver development J:83727
abnormal skeleton development J:83727
abnormal spleen morphology J:83727
abnormal sternum morphology J:83727
abnormal trochanter morphology J:83727
absent deltoid tuberosity J:83727
decreased myocardial fiber number J:83727
decreased spleen white pulp amount J:83727
lethality throughout fetal growth and development, incomplete penetrance J:83727
muscular ventricular septal defect J:83727
rib fusion J:83727
trabecula carnea hypoplasia J:83727
ventricle myocardium hypoplasia J:83727
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
11/19/2024
MGI 6.24 		The Jackson Laboratory