Symbol Name ID |
Fanca
Fanconi anemia, complementation group A MGI:1341823 |
* | Aspects of the system are reported to show a normal phenotype. |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Frontal bossing |
Dolichocephaly |
Micrognathia |
Microcephaly |
Clinodactyly of the 5th finger |
Complete duplication of thumb phalanx |
Abnormal thumb morphology |
Triphalangeal thumb |
Absent thumb |
Short thumb |
Aplasia/Hypoplasia of fingers |
Clubbing of toes |
Toe syndactyly |
Finger syndactyly |
Abnormal femur morphology |
Aplasia/Hypoplasia of the radius |
Absent radius |
Abnormal morphology of ulna |
Hypoplasia of the ulna |
Hip dislocation |
Scoliosis |
Back pain |
Reduced bone mineral density |
Disease(s) Associated with FANCA | |||||||||||||||||||||||
Fanconi anemia | |||||||||||||||||||||||
Fanconi anemia complementation group A | |||||||||||||||||||||||
pancreatic cancer |
Mouse Phenotypes | skeleton phenotype |
abnormal cranium morphology |
|
Availability | Mouse Genotype | ||
Fancatm1.1Wong/Fancatm1.1Wong | ! | ||
Fancatm1Faw/Fancatm1Faw | * | ||
Fancatm1Wong/Fancatm1Wong |
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 05/14/2024 MGI 6.23 |
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