Symbol Name ID |
Kif21a
kinesin family member 21A MGI:109188 |
Darker colors indicate more annotations |
Human Phenotypes | Esotropia |
Secondary esotropia |
Exotropia |
Sensory exotropia |
Compensatory chin elevation |
Restrictive external ophthalmoplegia |
Bilateral ptosis |
Disease(s) Associated with KIF21A | |||||||
congenital fibrosis of the extraocular muscles 1 |
Mouse Phenotypes | abnormal extraocular muscle morphology |
abnormal eye morphology |
blepharoptosis |
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Availability | Mouse Genotype | |||
Kif21atm1.1Ece/Kif21atm1.1Ece | ||||
Kif21atm1.1Ece/Kif21atm1.1Ece Tg(Isl1-EGFP*)1Slp/0 |
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Kif21atm1.1Ece/Kif21a+ | ||||
Kif21atm1.1Ece/Kif21atm3Ece |
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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