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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Crlf1tm1Wsa
targeted mutation 1, Warren S Alexander
MGI:2387956
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Crlf1tm1Wsa/Crlf1tm1Wsa involves: 129S1/Sv * C57BL/6 MGI:3618102


Genotype
MGI:3618102
hm1
Allelic
Composition
Crlf1tm1Wsa/Crlf1tm1Wsa
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Crlf1tm1Wsa mutation (0 available); any Crlf1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at birth, homozygotes are present at the expected Mendelian frequency; however, no homozygotes survive beyond 24 hrs after birth

behavior/neurological
• newborn homozygotes contain no milk in their stomachs
• newborn homozygotes open and close their mouths but fail to suckle effectively, despite the absence of gross or histologic abnormalities in brain (i.e. cortex and hippocampus), olfactory bulb, as well as facial or mouth tissues

nervous system
• newborn homozygotes display a significantly reduced number of motoneurons in the lumbar spinal cord, with no apparent change in the brachial or thoracic cord
• newborn homozygotes also exhibit a significant decrease in the number of motoneurons in the facial but not hypoglossal nucleus; sensory neurons of the dorsal root ganglia remain unaffected

hematopoietic system
• newborn homozygotes display reduced numbers of hemopoietic progenitor cells in the bone marrow and spleen
• no differences in the numbers and lineage commitment of progenitor cells are observed in neonatal liver





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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
11/19/2024
MGI 6.24
The Jackson Laboratory