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Symbol
Name
ID
Knl1
kinetochore scaffold 1
MGI:1923714
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Hypertelorism
Disease(s) Associated with KNL1
primary autosomal recessive microcephaly 4

Mouse Phenotypes
abnormal lens morphology
cataract
Availability Mouse Genotype
Knl1tm1b(EUCOMM)Hmgu/Knl1+

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
09/22/2020
MGI 6.16
The Jackson Laboratory