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TiparpGt(ROSA)79Sor
Gene trapped Allele Detail
Summary
Symbol: TiparpGt(ROSA)79Sor
Name: TCDD-inducible poly(ADP-ribose) polymerase; gene trapped 79, Philippe Soriano
MGI ID: MGI:3526866
Synonyms: Tiparp-
Gene: Tiparp  Location: Chr3:65435868-65462939 bp, + strand  Genetic Position: Chr3, 30.2 cM
Alliance: TiparpGt(ROSA)79Sor page
Mutation
origin
Mutant Cell Line:  S4-9E1
Germline Transmission:  Earliest citation of germline transmission: J:117491
Parent Cell Line:  AK7.1 (ES Cell)
Strain of Origin:  129S4/SvJaeSor
Mutation
description
Allele Type:    Gene trapped (Null/knockout, Reporter)
Mutation:    Insertion of gene trap vector     Vector: ROSAFARY
 
Mutation detailsThe Rosafary gene trap vector containing a SAbetaGeo pA promoter trap module and a PGKhygSD poly-A trap module was inserted into intron 1. (J:117491)
Sequence Tags: 
Sequence tag details (1 tag)
Genome Context: 
Genome Browser view of this mutation
Phenotypes
Key:
hm homozygous ht heterozygous tg involves transgenes phenotype observed
cn conditional genotype  cx complex: > 1 genome feature ot other: hemizygous, indeterminate,... N normal phenotype
Genotype/
Background:
Allelic Composition
Genetic Background
Cell Line(s)
Allelic CompositionGenetic BackgroundCell Line(s)
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
 
involves: 129S4/SvJaeSor
 
involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6J
 
either: (involves: 129S4/SvJaeSor * 129S7/SvEvBrd) or (involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6)
 
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
 
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
 
involves: 129S4/SvJaeSor
 
Phenotypes:
Affected Systems
show or hide all annotated terms Sex:
           
cardiovascular system
abnormal blood vessel morphology
hemorrhage
craniofacial
abnormal neurocranium morphology
abnormal frontal bone morphology
small presphenoid bone
short premaxilla
short maxilla
short nasal bone
abnormal palate morphology
decreased palatine bone horizontal plate size
broad snout
short snout
digestive/alimentary system
abnormal palate morphology
decreased palatine bone horizontal plate size
endocrine/exocrine glands
increased corpora lutea number
increased tertiary ovarian follicle number
enlarged ovary
hemorrhagic ovary cyst
abnormal thymus involution
growth/size/body
short nasal bone
abnormal palate morphology
decreased palatine bone horizontal plate size
broad snout
short snout
enlarged ovary
hemorrhagic ovary cyst
increased susceptibility to weight loss
enlarged liver
hematopoietic system
abnormal thymus involution
anemia
decreased erythrocyte cell number
decreased hematocrit
decreased hemoglobin content
polychromatophilia
reticulocytosis
homeostasis/metabolism
increased blood urea nitrogen level
decreased fasting circulating glucose level
decreased circulating estradiol level
increased circulating alanine transaminase level
increased susceptibility to xenobiotic induced morbidity/mortality
increased physiological sensitivity to xenobiotic
immune system
abnormal thymus involution
kidney inflammation
liver/biliary system
enlarged liver
hepatic steatosis
liver degeneration
mortality/aging
increased susceptibility to xenobiotic induced morbidity/mortality
postnatal lethality
muscle
abnormal smooth muscle morphology
renal/urinary system
kidney inflammation
abnormal kidney morphology
abnormal renal glomerulus morphology
small kidney
pale kidney
reproductive system
N
reproductive system phenotype
N
increased corpora lutea number
increased tertiary ovarian follicle number
enlarged ovary
hemorrhagic ovary cyst
enlarged uterus
long gestation period
prolonged estrous cycle
female infertility
reduced female fertility
decreased litter size
respiratory system
short nasal bone
skeleton
abnormal skeleton morphology
abnormal neurocranium morphology
abnormal frontal bone morphology
small presphenoid bone
short premaxilla
short maxilla
short nasal bone
decreased palatine bone horizontal plate size
abnormal sternum morphology
asymmetric sternocostal joints
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 20 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Tiparp Mutation:  43 strains or lines available
References
Original:  J:117491 Schmahl J, et al., PDGF signaling specificity is mediated through multiple immediate early genes. Nat Genet. 2007 Jan;39(1):52-60
All:  4 reference(s)

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
12/17/2024
MGI 6.24
The Jackson Laboratory

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