Phenotypes associated with this allele

• Allele Symbol: Nil
• Allele Name: neonatal intestinal lipidosis
• Allele ID: MGI:1861185
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Nil/Nil	involves: A/Cam	MGI:3768638
ht2	Nil/Nil^+	involves: A/Cam	MGI:3768637

Genotype
MGI:3768638

hm1

• Allelic Composition: Nil/Nil
• Genetic Background: involves: A/Cam

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

mortality/aging

embryonic lethality, complete penetrance ( J:5144 )

• die at or before E11

Genotype
MGI:3768637

ht2

• Allelic Composition: Nil/Nil⁺
• Genetic Background: involves: A/Cam

mortality/aging

premature death ( J:5144 )

• Background Sensitivity: life-span is shortened

digestive/alimentary system

abnormal intestine morphology ( J:33328 )

• portions of intestinal wall are thicker

abnormal small intestine morphology ( J:33328 )

abnormal intestinal lipid absorption ( J:33328 )

• Background Sensitivity: varying degree of lipidosis in the small intestine, especially in the submucosa

homeostasis/metabolism

abnormal intestinal lipid absorption ( J:33328 )

• Background Sensitivity: varying degree of lipidosis in the small intestine, especially in the submucosa

growth/size/body

growth/size/body region phenotype ( J:5144 )

N • Background Sensitivity: mice are small as adults

postnatal growth retardation ( J:5144 )

reproductive system

reduced fertility ( J:5144 )

• Background Sensitivity: depends on background