Symbol Name ID |
Ror2
receptor tyrosine kinase-like orphan receptor 2 MGI:1347521 |
Darker colors indicate more annotations |
Human Phenotypes | Atrial septal defect |
Ventricular septal defect |
Tetralogy of Fallot |
Abnormal tricuspid valve morphology |
Abnormal pulmonary valve morphology |
Abnormal aortic morphology |
Right ventricular outlet tract obstruction |
Disease(s) Associated with ROR2 | |||||||
autosomal recessive Robinow syndrome | |||||||
brachydactyly type B1 |
Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal placenta vasculature |
transposition of great arteries |
perimembraneous ventricular septal defect |
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Availability | Mouse Genotype | ||||
Ror2em1(IMPC)Mbp/Ror2em1(IMPC)Mbp | |||||
Ror2tm1Ymi/Ror2tm1Ymi | |||||
Ror2em1(IMPC)Mbp/Ror2+ |
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 04/23/2024 MGI 6.23 |
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