Symbol Name ID |
Frem2
Fras1 related extracellular matrix protein 2 MGI:2444465 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Cutaneous syndactyly |
Disease(s) Associated with FREM2 | |
Fraser syndrome 2 |
Mouse Phenotypes | limbs/digits/tail phenotype |
abnormal limb morphology |
abnormal digit morphology |
fused phalanges |
oligodactyly |
polydactyly |
preaxial polydactyly |
syndactyly |
clubfoot |
|
Availability | Mouse Genotype | |||||||||
Frem2b2b1562Clo/Frem2b2b1562Clo | ||||||||||
Frem2em2Hali/Frem2em2Hali | * | |||||||||
Frem2my-F11/Frem2my-F11 | ||||||||||
Frem2my-Ucl/Frem2my-Ucl | ||||||||||
Frem2my/Frem2my | ||||||||||
Frem2ne/Frem2ne | ||||||||||
Frem2em1Hali/Frem2em2Hali |
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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