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Symbol
Name
ID
Epb41l1
erythrocyte membrane protein band 4.1 like 1
MGI:103010
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Deeply set eye
Hypertelorism
Disease(s) Associated with EPB41L1
autosomal dominant intellectual developmental disorder 11

Mouse Phenotypes
abnormal iris pigmentation
abnormal eyelid morphology
Availability Mouse Genotype
Epb41l1tm1b(EUCOMM)Wtsi/Epb41l1tm1b(EUCOMM)Wtsi

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
04/30/2024
MGI 6.23
The Jackson Laboratory