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Symbol Name ID |
Efemp2
epidermal growth factor-containing fibulin-like extracellular matrix protein 2 MGI:1891209 |
| Darker colors indicate more annotations |
| Human Phenotypes | Keratoconus |
Astigmatism |
Retinoblastoma |
Hypertelorism |
Proptosis |
Myopia |
| Disease(s) Associated with EFEMP2 | ||||||
| arterial tortuosity syndrome | ||||||
| autosomal recessive cutis laxa type IB | ||||||
| osteosarcoma |
| Mouse Phenotypes | blepharoptosis |
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| Availability | Mouse Genotype | |
| Efemp2tm1.1Chu/Efemp2tm1.1Chu | ||
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 04/30/2024 MGI 6.23 |
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