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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nlrp12tm1Tdk
targeted mutation 1, Thirumala-Devi Kanneganti
MGI:5305143
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nlrp12tm1Tdk/Nlrp12tm1Tdk B6.Cg-Nlrp12tm1Tdk MGI:5305144


Genotype
MGI:5305144
hm1
Allelic
Composition
Nlrp12tm1Tdk/Nlrp12tm1Tdk
Genetic
Background
B6.Cg-Nlrp12tm1Tdk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nlrp12tm1Tdk mutation (0 available); any Nlrp12 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• following DSS treatment
• in DSS treated mice production of proinflammatory cytokines is increased in the colon
• in DSS treated mice production of chemokines is increased in the colon
• mesenteric lymph nodes and spleen are heavier and enlarged 2 weeks after DSS administration is stopped indicating a prolonged inflammatory response
• unlike wild-type mice, mutant mice suffer from continued body weight loss, diarrhea, and rectal bleeding following removal of DSS from the water
• mice continue to show inflammation in the colon 2 weeks after DSS administration is stopped
• colons contain more infiltrating inflammatory cells and display more ulceration and hyperplasia during the recovery phase of DSS induced colitis but not during the early stage
• body weight of chimeric mice with wild-type hematopoietic cells eventually recovers to levels similar to wild-type mice, unlike non-chimeric mutant mice

homeostasis/metabolism
• in DSS treated mice production of proinflammatory cytokines is increased in the colon
• in DSS treated mice production of chemokines is increased in the colon
• following azoxymethane and DSS treatment mice have increase tumor burden in the colon, lose more weight, and show increased rectal bleeding
• following azoxymethane and DSS treatment mice show tumors throughout the colonic tract unlike wild-type mice where the tumors are mostly contained within the rectal and distal areas of the colon
• following azoxymethane and DSS treatment more mice develop high grade dysplasia, about 30% of which are classified as adenocarcinomas, compared to wild-type controls
• tumor burden is not increased in azoxymethane and DSS treated chimeric mice with wild-type hematopoietic cells

hematopoietic system
• following DSS treatment

digestive/alimentary system
• unlike wild-type mice, mutant mice suffer from continued body weight loss, diarrhea, and rectal bleeding following removal of DSS from the water
• mice continue to show inflammation in the colon 2 weeks after DSS administration is stopped
• colons contain more infiltrating inflammatory cells and display more ulceration and hyperplasia during the recovery phase of DSS induced colitis but not during the early stage
• body weight of chimeric mice with wild-type hematopoietic cells eventually recovers to levels similar to wild-type mice, unlike non-chimeric mutant mice

neoplasm
• following azoxymethane and DSS treatment mice have increase tumor burden in the colon, lose more weight, and show increased rectal bleeding
• following azoxymethane and DSS treatment mice show tumors throughout the colonic tract unlike wild-type mice where the tumors are mostly contained within the rectal and distal areas of the colon
• following azoxymethane and DSS treatment more mice develop high grade dysplasia, about 30% of which are classified as adenocarcinomas, compared to wild-type controls
• tumor burden is not increased in azoxymethane and DSS treated chimeric mice with wild-type hematopoietic cells

growth/size/body
• following DSS treatment





Contributing Projects:
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
05/07/2024
MGI 6.23
The Jackson Laboratory