Symbol Name ID |
Abca12
ATP-binding cassette, sub-family A member 12 MGI:2676312 |
Darker colors indicate more annotations |
Human Phenotypes | Hepatosplenomegaly |
Short stature |
Failure to thrive |
Disease(s) Associated with ABCA12 | |||
autosomal recessive congenital ichthyosis 1 | |||
autosomal recessive congenital ichthyosis 4A | |||
autosomal recessive congenital ichthyosis 4B |
Mouse Phenotypes | abnormal facial morphology |
eclabion |
abnormal outer ear morphology |
decreased birth weight |
decreased fetal size |
decreased fetal weight |
|
Availability | Mouse Genotype | ||||||
Abca12el12/Abca12el12 | |||||||
Abca12em1(IMPC)J/Abca12em1(IMPC)J | |||||||
Abca12tm1Shzu/Abca12tm1Shzu |
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 04/16/2024 MGI 6.23 |
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