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Symbol
Name
ID
Epb41l1
erythrocyte membrane protein band 4.1 like 1
MGI:103010
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties in infancy
Atypical behavior
Disease(s) Associated with EPB41L1
autosomal dominant intellectual developmental disorder 11

Mouse Phenotypes
increased exploration in new environment
decreased thigmotaxis
increased startle reflex
decreased grip strength
abnormal locomotor behavior
hyperactivity
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
04/09/2024
MGI 6.23
The Jackson Laboratory