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Symbol
Name
ID
Abhd5
abhydrolase domain containing 5
MGI:1914719
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Everted lower lip vermilion
Eclabion
Abnormality of the dentition
Aplasia/Hypoplasia of the eyebrow
Ectropion
Disease(s) Associated with ABHD5
autosomal recessive congenital ichthyosis 1
Chanarin-Dorfman syndrome

Mouse Phenotypes
abnormal maxilla morphology
Availability Mouse Genotype
Abhd5tm1a(KOMP)Wtsi/Abhd5tm1a(KOMP)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
04/23/2024
MGI 6.23
The Jackson Laboratory