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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mllt3tm1Thr
targeted mutation 1, Terence H Rabbitts
MGI:2388981
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mllt3tm1Thr/Mllt3tm1Thr involves: 129S/SvEv * C57BL/6 MGI:3833416


Genotype
MGI:3833416
hm1
Allelic
Composition
Mllt3tm1Thr/Mllt3tm1Thr
Genetic
Background
involves: 129S/SvEv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mllt3tm1Thr mutation (0 available); any Mllt3 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about half are found dead at birth or die within a few hours of birth
• about half are found dead at birth or die within a few hours of birth
• no mice survive to weaning

growth/size/body
• mice that survive past bthe perinatal period become severely runted by 2 weeks of age

skeleton
• in newborns, sternums consist mainly of bone rather than bone and cartilage
• C8 has rib anlagen that does not attach to the sternum or to the first pair of thoracic ribs
• lack a pair of floating ribs
• in the region of C3 to C8 the spinal column is compressed causing an S shaped deformation of the neck and forward tilt of the head
• most mice are missing a vertebra, associated with loss of a pair of floating ribs
• S shaped deformation of the neck and forward tilt of the head
• C3 looks more like C2 than C4 with a round rather than oval cross sectional shape
• in all cases C1 is about twice as tall as in wild-type controls
• C1 has the appearance of 2 partially fused vertebrae
• malformations of C2 are sometimes seen
• in a few cases C2 looks like 2 partially fused vertebrae
• in some cases C2 and C3 appear partially fused
• anterior homeotic transformation from C3 through T13
• however, lumbar and caudal vertebrae appear similar to controls
• most mice have an extra cervical vertebra compensating for loss of a thoracic vertebra
• the spinous process usually found of T2 is seen on T3

embryo
• in situ hybridization analysis of E9.5 mutant embryos revealed a posterior shift in the anterior expression limits of Hoxd4, corresponding to approximately one rhombomere, indicating altered embryo patterning

hematopoietic system
N
• mutant neonates displayed normal hematopoiesis, as shown by histology and flow cytometry





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory