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Symbol
Name
ID
Rft1
RFT1 homolog
MGI:3607791
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Abnormal posterior cranial fossa morphology
Microcephaly
Short neck
Adducted thumb
Arthrogryposis multiplex congenita
Disease(s) Associated with RFT1
congenital disorder of glycosylation In

Mouse Phenotypes
long tibia
Availability Mouse Genotype
Rft1tm1b(KOMP)Wtsi/Rft1+

Contributing Projects:
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
04/09/2024
MGI 6.23
The Jackson Laboratory