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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Kittm2Bsm
targeted mutation 2, Peter Besmer
MGI:2663995
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Kittm2Bsm/Kit+ involves: 129X1/SvJ * C57BL/6J MGI:2663997


Genotype
MGI:2663997
ht1
Allelic
Composition
Kittm2Bsm/Kit+
Genetic
Background
involves: 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kittm2Bsm mutation (0 available); any Kit mutation (182 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• starting at 4 weeks of age, heterozygotes develop symptoms of disease and eventually die from pathology in the GI tract, showing a 50% survival rate at 9 months of age

digestive/alimentary system
• 7 of 14 heterozygotes exhibit a well-defined, black-pigmented distal esophagus at the gastro-esophageal junction
• EM analysis indicates melanosomes, discontinuous external lamina, short cell processes, and single centrally located nucleoli
• all (14 of 14) heterozygotes exhibit a firm white nodular mass of variable size (1 mm to 2 cm) in the cecum
• 9 of 14 heterozygotes display a distended cecum with clear fluid or pus-like contents
• atrophy of the colonic folds, lumen distension, and in one case abscess formation associated with acute serositis are observed
• 9 of 14 heterozygotes display an enlarged cecum
• 12 of 14 heterozygotes display variable distention of the distal ileum (mega-ileum) ending at the level of the cecum
• however, the remaining small intestine, stomach, colon, and anus appear morphologically normal
• heterozygotes exhibit neoplastic lesions of GISTs predominantly in the myenteric plexus of the cecum

neoplasm
• heterozygotes exhibit neoplastic lesions of GISTs predominantly in the myenteric plexus of the cecum

pigmentation
• 7 of 14 heterozygotes display hypepigmentation of the distal esophagus at the gastro-esophageal junction
• 5 of 6 heterozygotes with a dark distal esophagus contain melanosomes specifically within the myenteric plexus
• pigmented areas of the esophageal myenteric plexus contain large, ovoid cells with abundant cytoplasm filled with numerous stage IV melanosomes, and are surrounded by a discontinuous linear basal lamina
• pigmented cells are intermixed with other cell components of the myenteric plexus, including Schwann cells, axonal processes, and interstitial cells of Cajal

immune system
• heterozygotes exhibit extracellular granules in the vicinity of mast cells in the dorsal skin
• heterozygotes show a 4-fold increase in the number of mast cells in the dorsal skin and peritoneum

hematopoietic system
• heterozygotes exhibit extracellular granules in the vicinity of mast cells in the dorsal skin
• heterozygotes show a 4-fold increase in the number of mast cells in the dorsal skin and peritoneum

reproductive system
• both male and female heterozygotes are fertile but display a progressive decline in fertility with increasing age

nervous system
• all (6 of 6) heterozygotes display patchy hyperplasia of the myenteric plexus of the stomach, cecum and large intestine
• 3 of 6 heterozygotes display hyperplasia of the myenteric plexus in the proximal duodenum
• however, no myenteric plexus hyperplasia is observed in the morphologically normal distal duodenum, jejunum, and distended ileum
• in addition, 5 of 6 heterozygotes exhibit patchy thickening/hyperplasia of the esophageal myenteric plexus, and hyperpigmented cells are found specifically within the myenteric plexus of the of distal esophagus

cellular
• heterozygotes exhibit extracellular granules in the vicinity of mast cells in the dorsal skin

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
gastrointestinal stromal tumor DOID:9253 OMIM:606764
J:83616





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory