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Symbol Name ID |
Tfrc
transferrin receptor MGI:98822 |
| Darker colors indicate more annotations |
| Human Phenotypes | Conjunctivitis |
| Disease(s) Associated with TFRC | |
| immunodeficiency 46 |
| Mouse Phenotypes | abnormal Meckel's cartilage morphology |
small Meckel's cartilage |
abnormal hyoid bone morphology |
abnormal mandible morphology |
abnormal mandibular angle morphology |
small mandibular condyloid process |
small mandibular coronoid process |
short mandible |
micrognathia |
abnormal gonial bone morphology |
abnormal secondary palate development |
failure of palatal shelf elevation |
complete cleft palate |
abnormal tongue morphology |
oral cleft |
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| Availability | Mouse Genotype | |||||||||||||||
| Tfrctm3.1Nca/Tfrctm3.1Nca H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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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 04/23/2024 MGI 6.23 |
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