About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rab27btm1.2Seab
targeted mutation 1.2, Miguel C Seabra
MGI:3706986
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rab27btm1.2Seab/Rab27btm1.2Seab involves: 129X1/SvJ * C57BL/6J MGI:3711073
cx2
Rab27aash/Rab27aash
Rab27btm1.2Seab/Rab27btm1.2Seab
involves: 129X1/SvJ * C3H/HeSn * C57BL/6J MGI:3711074


Genotype
MGI:3711073
hm1
Allelic
Composition
Rab27btm1.2Seab/Rab27btm1.2Seab
Genetic
Background
involves: 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab27btm1.2Seab mutation (4 available); any Rab27b mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• diminished platelet serotonin content
• significant bleeding defect in platelet function in vivo
• platelet number or size or gross morphology and alpha granule function were normal
• impaired aggregation with collage and U46619
• reduced secretion of dense granules

hematopoietic system
• 50% reduction in the number of dense granules per platelet
• diminished platelet serotonin content
• impaired aggregation with collage and U46619
• reduced secretion of dense granules

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
platelet storage pool deficiency DOID:2223 OMIM:185050
J:120307




Genotype
MGI:3711074
cx2
Allelic
Composition
Rab27aash/Rab27aash
Rab27btm1.2Seab/Rab27btm1.2Seab
Genetic
Background
involves: 129X1/SvJ * C3H/HeSn * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab27aash mutation (4 available); any Rab27a mutation (147 available)
Rab27btm1.2Seab mutation (4 available); any Rab27b mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• diminished platelet serotonin content
• significant bleeding defect in platelet function in vivo
• platelet number or size or gross morphology and alpha granule function were normal
• impaired aggregation with collagen and U46619
• reduced secretion of dense granules

hematopoietic system
• 50% reduction in the number of dense granules per platelet
• diminished platelet serotonin content
• impaired aggregation with collagen and U46619
• reduced secretion of dense granules

respiratory system
• reduced numbers and patchy distribution
• increased number and size of mature lamellar bodies
• thinning of bronchial epithelium
• disorganization and shortening of bronchioloar cilia
• enlargement of alveolar air spaces which becomes more evident with age
• reduced numbers of alveolar epithelial II cells and reduced numbers of Clare cells
• patchy ditribution of Clara cells

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
platelet storage pool deficiency DOID:2223 OMIM:185050
J:120307





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory