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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rab32tm1b(KOMP)Wtsi
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:5692679
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi C57BL/6N-Rab32tm1b(KOMP)Wtsi/Ucd MGI:5757595
ht2
Rab32tm1b(KOMP)Wtsi/Rab32+ C57BL/6N-Rab32tm1b(KOMP)Wtsi/Ucd MGI:5797759
cx3
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi
Rab38tm1.1Ics/Rab38tm1.1Ics
involves: C57BL/6N * C57BL/6NTac MGI:6491326
cx4
Rab32tm1b(KOMP)Wtsi/Rab32+
Rab38tm1.1Ics/Rab38tm1.1Ics
involves: C57BL/6N * C57BL/6NTac MGI:6491327
cx5
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi
Rab38tm1.1Ics/Rab38+
involves: C57BL/6N * C57BL/6NTac MGI:6491328


Genotype
MGI:5757595
hm1
Allelic
Composition
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi
Genetic
Background
C57BL/6N-Rab32tm1b(KOMP)Wtsi/Ucd
Cell Lines EPD0095_2_C12
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab32tm1b(KOMP)Wtsi mutation (1 available); any Rab32 mutation (16 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
IMPC - UCD

growth/size/body
IMPC - UCD

mortality/aging

renal/urinary system

reproductive system
IMPC - UCD




Genotype
MGI:5797759
ht2
Allelic
Composition
Rab32tm1b(KOMP)Wtsi/Rab32+
Genetic
Background
C57BL/6N-Rab32tm1b(KOMP)Wtsi/Ucd
Cell Lines EPD0095_2_C12
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab32tm1b(KOMP)Wtsi mutation (1 available); any Rab32 mutation (16 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological




Genotype
MGI:6491326
cx3
Allelic
Composition
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi
Rab38tm1.1Ics/Rab38tm1.1Ics
Genetic
Background
involves: C57BL/6N * C57BL/6NTac
Cell Lines EPD0095_2_C12
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab32tm1b(KOMP)Wtsi mutation (1 available); any Rab32 mutation (16 available)
Rab38tm1.1Ics mutation (0 available); any Rab38 mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• dense granules show an abnormal dense core having a very small, linear, or poorly condensed appearance instead of a typical bulls-eye appearance
• deficiency in dense granule biogenesis is already seen at the megakaryocyte stage in the bone marrow
• however, alpha granules have a normal appearance
• platelets show a total 75% decrease in ADP and 50% decrease in ATP content, thus the ATP/ADLP ratio is twice that of wild-type mice
• platelets show a total 75% decrease in ADP and 50% decrease in ATP content, thus the ATP/ADLP ratio is twice that of wild-type mice
• dense granule formation in platelets is impaired
• 70% decrease in the total number of dense granules in platelets
• dense granule 5-hydroxytryptamine (5-HT) storage is almost abolished in platelets
• however, total platelet factor 4 (PF4), P-selectin, fibrinogen, and VWF levels are normal in platelets
• platelets under flow form only a layer over the surface with no growth in height, indicating that initial platelet attachment is normal but is followed by a defect in thrombus growth
• -platelets exhibit decreased lysosomal exocytosis

homeostasis/metabolism
• platelets show a total 75% decrease in ADP and 50% decrease in ATP content, thus the ATP/ADLP ratio is twice that of wild-type mice
• dense granule 5-hydroxytryptamine (5-HT) storage is almost abolished in platelets
• however, total platelet factor 4 (PF4), P-selectin, fibrinogen, and VWF levels are normal in platelets
• platelets under flow form only a layer over the surface with no growth in height, indicating that initial platelet attachment is normal but is followed by a defect in thrombus growth
• -platelets exhibit decreased lysosomal exocytosis
• mice are resistant to thromboembolism induced by tissue factor administration
• thrombosis resulting from vessel injury is severely impaired
• thrombosis is impaired in a FeCl3-induced injury in the carotid, with no thrombus growth at all
• mice show an increase in bleeding time in a tail bleeding assay, with no cessation of bleeding after 30 minutes

integument
• mice exhibit severe coat color dilution, presenting a light beige pigmentation

pigmentation
• mice exhibit severe coat color dilution, presenting a light beige pigmentation
• mice exhibit severe eye dilution, presenting red eyes

respiratory system
• mice show impaired lung alveolar structure
• mice show alveolar type II cells containing enlarged lamellar bodies
• mice exhibit lung epithelium damage as evidenced by thickening of alveolar septa

vision/eye
• mice exhibit severe eye dilution, presenting red eyes

cellular
• platelets show a total 75% decrease in ADP and 50% decrease in ATP content, thus the ATP/ADLP ratio is twice that of wild-type mice

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Hermansky-Pudlak syndrome DOID:3753 OMIM:PS203300
J:293385




Genotype
MGI:6491327
cx4
Allelic
Composition
Rab32tm1b(KOMP)Wtsi/Rab32+
Rab38tm1.1Ics/Rab38tm1.1Ics
Genetic
Background
involves: C57BL/6N * C57BL/6NTac
Cell Lines EPD0095_2_C12
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab32tm1b(KOMP)Wtsi mutation (1 available); any Rab32 mutation (16 available)
Rab38tm1.1Ics mutation (0 available); any Rab38 mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• platelets show an approximate 30% decrease in dense granule ADP and 17% decrease in ATP content
• platelets show an approximate 30% decrease in dense granule ADP and 17% decrease in ATP content
• mice show a 32% decrease in platelet dense granule 5-HT content
• however, platelet dense granules have a normal morphology

homeostasis/metabolism
• platelets show an approximate 30% decrease in dense granule ADP and 17% decrease in ATP content
• mice show a 32% decrease in platelet dense granule 5-HT content
• however, platelet dense granules have a normal morphology

integument
• mice show an intermediate diluted coat color to that seen in double homozygous mice

pigmentation
• mice show an intermediate diluted coat color to that seen in double homozygous mice

cellular
• platelets show an approximate 30% decrease in dense granule ADP and 17% decrease in ATP content




Genotype
MGI:6491328
cx5
Allelic
Composition
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi
Rab38tm1.1Ics/Rab38+
Genetic
Background
involves: C57BL/6N * C57BL/6NTac
Cell Lines EPD0095_2_C12
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab32tm1b(KOMP)Wtsi mutation (1 available); any Rab32 mutation (16 available)
Rab38tm1.1Ics mutation (0 available); any Rab38 mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• platelets show a 45% decrease in ADP and 20% decrease in ATP content
• platelets show a 45% decrease in ADP and 20% decrease in ATP content
• mice show a 40% decrease in platelet dense granule 5-HT content
• however, platelet dense granules have a normal morphology

homeostasis/metabolism
• platelets show a 45% decrease in ADP and 20% decrease in ATP content
• mice show a 40% decrease in platelet dense granule 5-HT content
• however, platelet dense granules have a normal morphology

integument
• mice exhibit less pigment dilution than double homozygotes, similar to single homozygous Rab38 mutant mice

pigmentation
• mice exhibit less pigment dilution than double homozygotes, similar to single homozygous Rab38 mutant mice

cellular
• platelets show a 45% decrease in ADP and 20% decrease in ATP content





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory