About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hprt1tm1(Pck1-cre)Vhh
targeted mutation 1, Volker H Haase
MGI:3621174
Summary 9 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Mioxtm1Ysk/Mioxtm1Ysk
Hprt1tm1(Pck1-cre)Vhh/Hprt1+
B6.129-Mioxtm1Ysk Hprt1tm1(Pck1-cre)Vhh MGI:6267414
cn2
Dicer1tm1Bdh/Dicer1tm1Bdh
Hprt1tm1(Pck1-cre)Vhh/Y
involves: 129 * 129P2/OlaHsd MGI:5437747
cn3
Agtr1atm1.1Cof/Agtr1atm1.1Cof
Hprt1tm1(Pck1-cre)Vhh/Hprt1+
involves: 129 * 129P2/OlaHsd MGI:5007681
cn4
Hif1atm3Rsjo/Hif1atm3Rsjo
Hprt1tm1(Pck1-cre)Vhh/Y
Vhltm1Jae/Vhltm1Jae
involves: 129 * BALB/c * C57BL/6 MGI:3621461
cn5
Arnttm1Bra/Arnttm1Bra
Hprt1tm1(Pck1-cre)Vhh/Y
Vhltm1Jae/Vhltm1Jae
involves: 129 * BALB/c * C57BL/6 MGI:3621462
cn6
Hif1atm3Rsjo/Hif1atm3Rsjo
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Hprt1tm1(Pck1-cre)Vhh/Y
involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ MGI:4418525
cn7
Hprt1tm1(Pck1-cre)Vhh/Y
Vhltm1Jae/Vhltm1Jae
involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6 MGI:3621460
cn8
Hprt1tm1(Pck1-cre)Vhh/Hprt1+
Tg(CAG-lacZ,-Miox)#Ysk/0
involves: 129P2/OlaHsd * C57BL/6J MGI:6267415
cn9
Pdss2tm1Dalg/Pdss2tm1Dalg
Hprt1tm1(Pck1-cre)Vhh/?
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3805707


Genotype
MGI:6267414
cn1
Allelic
Composition
Mioxtm1Ysk/Mioxtm1Ysk
Hprt1tm1(Pck1-cre)Vhh/Hprt1+
Genetic
Background
B6.129-Mioxtm1Ysk Hprt1tm1(Pck1-cre)Vhh
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
Mioxtm1Ysk mutation (0 available); any Miox mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• mice exhibit ameliorated cisplatin-induced acute kidney injury with reduced weight loss and minimal elevation of serum creatinine or urea levels, and mild cytolysis of tubular cells and loss of brush border but no renal tubular cell apoptosis or induction of reactive oxygen species generation compared with wild-type mice

growth/size/body




Genotype
MGI:5437747
cn2
Allelic
Composition
Dicer1tm1Bdh/Dicer1tm1Bdh
Hprt1tm1(Pck1-cre)Vhh/Y
Genetic
Background
involves: 129 * 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dicer1tm1Bdh mutation (4 available); any Dicer1 mutation (96 available)
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
N
• mice exhibit normal kidney size, renal histology, and renal function throughout a 6-month observation period
• at 8-10 weeks of age, BUN levels and serum creatinine levels are normal relative to those in wild-type controls
• following bilateral kidney ischemia/reperfusion injury, mice exhibit decreased creatinine plasma levels, significantly less cortical and outer medulla tubular damage, lower tubular apoptosis, and improved survival relative to wild-type controls

homeostasis/metabolism
• following bilateral kidney ischemia/reperfusion injury, mice exhibit decreased creatinine plasma levels, significantly less cortical and outer medulla tubular damage, lower tubular apoptosis, and improved survival relative to wild-type controls




Genotype
MGI:5007681
cn3
Allelic
Composition
Agtr1atm1.1Cof/Agtr1atm1.1Cof
Hprt1tm1(Pck1-cre)Vhh/Hprt1+
Genetic
Background
involves: 129 * 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agtr1atm1.1Cof mutation (0 available); any Agtr1a mutation (40 available)
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• decreased during both the night and day
• responses to high salt diet and vasoconstrictors are similar to wild-type controls

renal/urinary system
• absolute rates of proximal fluid reabsorption are reduced
• fractional reabsorption rates, corrected for single nephron glomerular filtration rate, are reduced
• decrease in single nephron glomerular filtration rate in the proximal tubules

homeostasis/metabolism
• absolute rates of proximal fluid reabsorption are reduced
• fractional reabsorption rates, corrected for single nephron glomerular filtration rate, are reduced




Genotype
MGI:3621461
cn4
Allelic
Composition
Hif1atm3Rsjo/Hif1atm3Rsjo
Hprt1tm1(Pck1-cre)Vhh/Y
Vhltm1Jae/Vhltm1Jae
Genetic
Background
involves: 129 * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hif1atm3Rsjo mutation (3 available); any Hif1a mutation (50 available)
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
Vhltm1Jae mutation (2 available); any Vhl mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• pockets of inflammation
• dilated lymphatic vessels
• unilateral and bilateral macroscopic cysts that vary in number and size are seen in 3 of 10 mice
• multiple microscopic cysts are also seen with 3 of 10 having cysts of tubular origin and 7 of 10 having cysts of glomerular origin
• cysts of both tubular and glomerular origin may occur in the same mouse

liver/biliary system
• cavernous hepatic hemangiomas seen in mice at 2 - 6 months of age and with increased frequency in mice older than 6 months

cardiovascular system
• proliferation of endothelial cells in hepatic blood vessels
• hepatic vascular angiectasia

neoplasm
• cavernous hepatic hemangiomas seen in mice at 2 - 6 months of age and with increased frequency in mice older than 6 months

hematopoietic system
• average red blood cell count is 10.77 x 106 compared to 9.3 x 106 in controls
• develop erythrocytosis as indicated by reddening of paws and muzzle
• hemoglobin content is 19.38 g/dl compared to 13.24 g/dl in controls

immune system
• pockets of inflammation

muscle
• hepatic vascular angiectasia

growth/size/body
• unilateral and bilateral macroscopic cysts that vary in number and size are seen in 3 of 10 mice
• multiple microscopic cysts are also seen with 3 of 10 having cysts of tubular origin and 7 of 10 having cysts of glomerular origin
• cysts of both tubular and glomerular origin may occur in the same mouse

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
von Hippel-Lindau disease DOID:14175 OMIM:193300
J:97652 , J:106705




Genotype
MGI:3621462
cn5
Allelic
Composition
Arnttm1Bra/Arnttm1Bra
Hprt1tm1(Pck1-cre)Vhh/Y
Vhltm1Jae/Vhltm1Jae
Genetic
Background
involves: 129 * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Arnttm1Bra mutation (0 available); any Arnt mutation (65 available)
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
Vhltm1Jae mutation (2 available); any Vhl mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
N
• no macroscopic or microscopic renal cysts are detected

liver/biliary system
• moderate steatosis without angiectasia or endothelial cell proliferation is seen only in mutants over 9 months of age

neoplasm
N
• no hepatic hemangiomas are seen

hematopoietic system
N
• red cell count and hemoglobin levels are similar to controls




Genotype
MGI:4418525
cn6
Allelic
Composition
Hif1atm3Rsjo/Hif1atm3Rsjo
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Hprt1tm1(Pck1-cre)Vhh/Y
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1Sor mutation (7 available); any Gt(ROSA)26Sor mutation (993 available)
Hif1atm3Rsjo mutation (3 available); any Hif1a mutation (50 available)
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• after ureteral ligation, mice exhibit reduced fibrosis and inflammation compared with similarly treated Hif1atm3Rsjo/Hif1atm3Rsjo Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ mice
• after ureteral ligation, mice exhibit reduced fibrosis and inflammation compared with similarly treated Hif1atm3Rsjo/Hif1atm3Rsjo Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ mice

cellular
• hypoxic primary tubular epithelial cells fails to undergo an epithelial to mesenchyme transition unlike similarly treated cells from Hif1atm3Rsjo/Hif1atm3Rsjo Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ mice

homeostasis/metabolism
• after ureteral ligation, mice exhibit reduced fibrosis and inflammation compared with similarly treated Hif1atm3Rsjo/Hif1atm3Rsjo Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ mice

immune system
• after ureteral ligation, mice exhibit reduced fibrosis and inflammation compared with similarly treated Hif1atm3Rsjo/Hif1atm3Rsjo Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ mice




Genotype
MGI:3621460
cn7
Allelic
Composition
Hprt1tm1(Pck1-cre)Vhh/Y
Vhltm1Jae/Vhltm1Jae
Genetic
Background
involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
Vhltm1Jae mutation (2 available); any Vhl mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• pockets of inflammation
• dilated lymphatic vessels
• unilateral and bilateral macroscopic cysts that vary in number and size are seen in 4 of 22 mice
• multiple microscopic cysts are also seen with 5 of 20 having cysts of tubular origin and 7 of 20 having cysts of glomerular origin
• cysts of both tubular and glomerular origin may occur in the same mouse

liver/biliary system
• cavernous hepatic hemangiomas seen in mice at 2 - 6 months of age and with increased frequency in mice older than 6 months

cardiovascular system
• proliferation of endothelial cells in hepatic blood vessels
• hepatic vascular angiectasia

neoplasm
• cavernous hepatic hemangiomas seen in mice at 2 - 6 months of age and with increased frequency in mice older than 6 months

hematopoietic system
• average red blood cell count is 11.7 x 106 compared to 9.3 x 106 in controls
• develop erythrocytosis as indicated by reddening of paws and muzzle
• hemoglobin content is 20.05 g/dl compared to 13.24 g/dl in controls

immune system
• pockets of inflammation

muscle
• hepatic vascular angiectasia

growth/size/body
• unilateral and bilateral macroscopic cysts that vary in number and size are seen in 4 of 22 mice
• multiple microscopic cysts are also seen with 5 of 20 having cysts of tubular origin and 7 of 20 having cysts of glomerular origin
• cysts of both tubular and glomerular origin may occur in the same mouse

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
von Hippel-Lindau disease DOID:14175 OMIM:193300
J:97652 , J:106705




Genotype
MGI:6267415
cn8
Allelic
Composition
Hprt1tm1(Pck1-cre)Vhh/Hprt1+
Tg(CAG-lacZ,-Miox)#Ysk/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
Tg(CAG-lacZ,-Miox)#Ysk mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• induced by cisplatin

homeostasis/metabolism
• induced by cisplatin
• mice exhibit worsened cisplatin-induced acute kidney injury with increased weight loss, serum creatinine and urea levels, and fulminant apoptosis of renal tubular cells, and accentuated cytolysis of tubular cells with loss of brush border and reactive oxygen species generation compared with wild-type mice

cellular
• induced by cisplatin
• induced by cisplatin




Genotype
MGI:3805707
cn9
Allelic
Composition
Pdss2tm1Dalg/Pdss2tm1Dalg
Hprt1tm1(Pck1-cre)Vhh/?
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hprt1tm1(Pck1-cre)Vhh mutation (0 available); any Hprt1 mutation (1279 available)
Pdss2tm1Dalg mutation (0 available); any Pdss2 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
N
• kidney ultrastructure normal
• no evidence of nephritis

homeostasis/metabolism
N
• normal urine albumin levels





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
11/12/2024
MGI 6.24
The Jackson Laboratory