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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Abhd16atm1a(EUCOMM)Wtsi
targeted mutation 1a, Wellcome Trust Sanger Institute
MGI:4820220
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Abhd16atm1a(EUCOMM)Wtsi/Abhd16atm1a(EUCOMM)Wtsi C57BL/6N-Abhd16atm1a(EUCOMM)Wtsi/Wtsi MGI:6261781
hm2
Abhd16atm1a(EUCOMM)Wtsi/Abhd16atm1a(EUCOMM)Wtsi involves: C57BL/6N * C57BL/6NTac MGI:5817019


Genotype
MGI:6261781
hm1
Allelic
Composition
Abhd16atm1a(EUCOMM)Wtsi/Abhd16atm1a(EUCOMM)Wtsi
Genetic
Background
C57BL/6N-Abhd16atm1a(EUCOMM)Wtsi/Wtsi
Cell Lines EPD0605_5_A11
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Abhd16atm1a(EUCOMM)Wtsi mutation (1 available); any Abhd16a mutation (23 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue

growth/size/body

homeostasis/metabolism

mortality/aging

reproductive system
IMPC - WTSI




Genotype
MGI:5817019
hm2
Allelic
Composition
Abhd16atm1a(EUCOMM)Wtsi/Abhd16atm1a(EUCOMM)Wtsi
Genetic
Background
involves: C57BL/6N * C57BL/6NTac
Cell Lines EPD0605_5_A11
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Abhd16atm1a(EUCOMM)Wtsi mutation (1 available); any Abhd16a mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice are born at a significantly lower Mendelian frequency
• however, no evidence of increased postnatal lethality is observed

growth/size/body
• at P1 and 10 weeks of age, mice are significantly smaller than wild-type or heterozygous littermates
• mice are ~30% smaller throughout development and life
• both sexes show a significant reduction in body weight from weaning (4 weeks) to 10 weeks of age

homeostasis/metabolism
• mice exhibit significant reductions in most lysophosphatidylserines (lyso-PSs) measured in brain tissue
• similar reductions in lyso-PS lipids are detected in spinal cord; however, no changes in phosphatidylserines (PSs) or other (lyso)phospholipids are noted in CNS tissues
• thioglycollate-elicited peritoneal macrophages show a ~80% reduction in cellular and secreted lyso-PSs under either basal or LPS-stimulated conditions; however, no changes in PSs, free fatty acids, eicasonoids (PGE2, PGD2, LTB4 or TXB2) or other (lyso)phospholipids are observed
• macrophages treated with inhibitors (KC01 or KC02) show no significant changes in lyso-PS secretion or other secreted and cellular lipids relative to DMSO-treated control macrophages
• phosphatidylserine (PS) lipase activity is significantly reduced in brain and spinal cord membrane lysates relative to that in wild-type or heterozygous lysates
• thioglycollate-elicited peritoneal macrophages show greatly reduced PS lipase activity that is no longer elevated by LPS treatment, whereas LPS induces a significant increase in PS lipase activity in wild-type and heterozygous macrophages

immune system
• thioglycollate-elicited peritoneal macrophages show greatly reduced PS lipase activity that is no longer elevated by LPS treatment, whereas LPS induces a significant increase in PS lipase activity in wild-type and heterozygous macrophages
• macrophages show a ~80% reduction in cellular and secreted lyso-PSs under either basal or LPS-stimulated conditions; however, no changes in PSs, free fatty acids, eicasonoids (PGE2, PGD2, LTB4 or TXB2) or other (lyso)phospholipids are observed
• macrophages treated with inhibitors (KC01 or KC02) show no significant changes in lyso-PS secretion or other secreted and cellular lipids relative to DMSO-treated control macrophages
• thioglycollate-elicited peritoneal macrophages show a significant reduction in LPS-induced cytokine (TNF, IL-6 and IL-1 beta) release
• basal cytokine profiles are unaffected in vehicle (PBS)-treated macrophages
• macrophages treated with inhibitors (KC01 or KC02) show no significant changes in basal or LPS-induced cytokine (IL-6 and TNF) secretion relative to DMSO-treated control macrophages
• thioglycollate-elicited peritoneal macrophages show a significant reduction in LPS-induced IL-1 beta secretion
• thioglycollate-elicited peritoneal macrophages show a significant reduction in LPS-induced IL-6 secretion
• thioglycollate-elicited peritoneal macrophages show a significant reduction in LPS-induced TNF secretion

hematopoietic system
• thioglycollate-elicited peritoneal macrophages show greatly reduced PS lipase activity that is no longer elevated by LPS treatment, whereas LPS induces a significant increase in PS lipase activity in wild-type and heterozygous macrophages
• macrophages show a ~80% reduction in cellular and secreted lyso-PSs under either basal or LPS-stimulated conditions; however, no changes in PSs, free fatty acids, eicasonoids (PGE2, PGD2, LTB4 or TXB2) or other (lyso)phospholipids are observed
• macrophages treated with inhibitors (KC01 or KC02) show no significant changes in lyso-PS secretion or other secreted and cellular lipids relative to DMSO-treated control macrophages
• thioglycollate-elicited peritoneal macrophages show a significant reduction in LPS-induced cytokine (TNF, IL-6 and IL-1 beta) release
• basal cytokine profiles are unaffected in vehicle (PBS)-treated macrophages
• macrophages treated with inhibitors (KC01 or KC02) show no significant changes in basal or LPS-induced cytokine (IL-6 and TNF) secretion relative to DMSO-treated control macrophages

behavior/neurological
N
• despite their smaller size, mice exhibit normal cage behavior





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last database update
09/24/2024
MGI 6.24
The Jackson Laboratory