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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Marckstm1Pjb
targeted mutation 1, Perry J Blackshear
MGI:2176302
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Marckstm1Pjb/Marckstm1Pjb involves: 129P2/OlaHsd * C57BL/6J MGI:2176329


Genotype
MGI:2176329
hm1
Allelic
Composition
Marckstm1Pjb/Marckstm1Pjb
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Marckstm1Pjb mutation (0 available); any Marcks mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Coronal sections of brains from Marckstm1Pjb/Marckstm1Pjb mice at E18.5

mortality/aging
• most died on the day of birth
• none ever suckled

nervous system
• open neural tube seen in various areas of the forebrain, midbrain, and hindbrain at E9.5
• excessive blebbing at the boundary between the surface ectoderm and neuroepithelium
• boundry between the cortical plate and the marginal zone is irregular (J:22949)
• most prominent in the parietal cortex and hippocampus (J:22949)
• decreased thickness of the marginal zone at E16.5 (J:40497)
• increased ventricular volume
• disrupted ventral hippocampal commissure
• anterior commissure disrupted
• abnormal separation of cerebral hemispheres
• seen in 25% of embryos from E12.5 onward
• percentage was higher in females than in males
• neuronal ectopia after E14.5
• some cases of neuroblasts growing through the basal lamina to the pial layer
• occasional neuronal growth into the subarachnoid space

craniofacial
• absence of scalp and skull in older fetuses with exencephaly

behavior/neurological
• newborns never suckled

vision/eye
• transient fiber layer of Chievitz lost in retinas at E18.5

embryo
• open neural tube seen in various areas of the forebrain, midbrain, and hindbrain at E9.5
• excessive blebbing at the boundary between the surface ectoderm and neuroepithelium

growth/size/body
• large herniation at the umbilicus
• high frequency
• decreased head size
• absence of scalp in older fetuses with exencephaly
• reduced crown to rump length in about 29% of mice

skeleton
• absence of scalp and skull in older fetuses with exencephaly





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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
11/12/2024
MGI 6.24
The Jackson Laboratory