| Human Disease |
Ichthyosis, Congenital, Autosomal Recessive 1; ARCI1 OMIM ID: 242300 |
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| Synonyms | Collodion Baby, Self-Healing; SHCB; Collodion Fetus; Desquamation of Newborn; Ichthyosis Congenita; Ichthyosis Congenita II; ICR2; Ichthyosis, Congenital, Autosomal Recessive 1, with Bathing Suit Distribution; Ichthyosis, Lamellar, 1, Formerly; LI1, FORMERLY; Lamellar Exfoliation of Newborn | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tgm1tm1Kfyn/Tgm1tm1Kfyn |
involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6 | J:45653, J:74334 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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