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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Washc5tm1.2Cbee
targeted mutation 1.2, Christian Beetz
MGI:6256428
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Washc5tm1.2Cbee/Washc5tm1.2Cbee involves: C57BL/6 MGI:6256430
ht2
Washc5tm1.2Cbee/Washc5+ involves: C57BL/6 MGI:6256431


Genotype
MGI:6256430
hm1
Allelic
Composition
Washc5tm1.2Cbee/Washc5tm1.2Cbee
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Washc5tm1.2Cbee mutation (0 available); any Washc5 mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no embryos are detected at E13.5 and no signs of terminated embryonic development in uteri suggesting lethality in very early embryonic stages




Genotype
MGI:6256431
ht2
Allelic
Composition
Washc5tm1.2Cbee/Washc5+
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Washc5tm1.2Cbee mutation (0 available); any Washc5 mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• foot-base angles do not differ from wild-type

cellular
N
• mouse adult fibroblasts grown in culture show unaltered endosomal tabulation and integrity of organelle compartments

growth/size/body
N
• mice exhibit normal body weight

nervous system
N
• cortical neurons grown in culture do not exhibit any abnormalities, showing normal axon length and number of axonal branches

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
NOT hereditary spastic paraplegia 8 DOID:0110823 OMIM:603563
J:266630





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory