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Symbol
Name
ID
Kctd1
potassium channel tetramerisation domain containing 1
MGI:1918269
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Cataract
Developmental cataract
Anisocoria
Iris coloboma
Hypotelorism
Disease(s) Associated with KCTD1
scalp-ear-nipple syndrome

Mouse Phenotypes
eye hemorrhage
corneal vascularization
sclerocornea
cataract
persistence of hyaloid vascular system
Availability Mouse Genotype
Kctd1em1(IMPC)J/Kctd1em1(IMPC)J

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
04/23/2024
MGI 6.23
The Jackson Laboratory