Symbol Name ID |
Fras1
Fraser extracellular matrix complex subunit 1 MGI:2385368 |
Darker colors indicate more annotations |
Human Phenotypes | Calvarial skull defect |
Microcephaly |
Encephalocele |
Aplasia/Hypoplasia of the phalanges of the hand |
Aplasia/Hypoplasia of the thumb |
Cutaneous finger syndactyly |
Wide pubic symphysis |
Aplasia/Hypoplasia of the sternum |
Disease(s) Associated with FRAS1 | ||||||||
Fraser syndrome 1 |
Mouse Phenotypes | micrognathia |
abnormal sternum morphology |
abnormal sternebra morphology |
abnormal rib morphology |
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Availability | Mouse Genotype | ||||
Fras1b2b3323Clo/Fras1b2b3323Clo | |||||
Fras1bfb/Fras1bfb |
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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