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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Aldh3a2tm1a(EUCOMM)Wtsi
targeted mutation 1a, Wellcome Trust Sanger Institute
MGI:4432633
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Aldh3a2tm1a(EUCOMM)Wtsi/Aldh3a2tm1a(EUCOMM)Wtsi C57BL/6N-Aldh3a2tm1a(EUCOMM)Wtsi/Ics MGI:5782020
cx2
Aldh3a2tm1a(EUCOMM)Wtsi/Aldh3a2tm1a(EUCOMM)Wtsi
Aldh3b2em1Akih/Aldh3b2em1Akih
involves: C57BL/6J * C57BL/6N MGI:7367456


Genotype
MGI:5782020
hm1
Allelic
Composition
Aldh3a2tm1a(EUCOMM)Wtsi/Aldh3a2tm1a(EUCOMM)Wtsi
Genetic
Background
C57BL/6N-Aldh3a2tm1a(EUCOMM)Wtsi/Ics
Cell Lines EPD0060_2_D02
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aldh3a2tm1a(EUCOMM)Wtsi mutation (1 available); any Aldh3a2 mutation (32 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

hematopoietic system

nervous system




Genotype
MGI:7367456
cx2
Allelic
Composition
Aldh3a2tm1a(EUCOMM)Wtsi/Aldh3a2tm1a(EUCOMM)Wtsi
Aldh3b2em1Akih/Aldh3b2em1Akih
Genetic
Background
involves: C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aldh3a2tm1a(EUCOMM)Wtsi mutation (1 available); any Aldh3a2 mutation (32 available)
Aldh3b2em1Akih mutation (1 available); any Aldh3b2 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice do not survive beyond P2 with absent milk spot and left outside of the nest

integument
• rougher in texture than control mice with shallow sulcus cutis

homeostasis/metabolism
• decreased acylceramide levels in the epidermis and stratum corneum
• however, mice exhibit normal levels of protein-bound ceramides in the epidermis
• increased level of many triglyceride species in the epidermis
• however, total triglyceride levels are normal

growth/size/body
• after birth

behavior/neurological
• associated with being left outside of the nest

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Sjogren-Larsson syndrome DOID:14501 OMIM:270200
J:330263





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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
The Jackson Laboratory