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Sparctm1Hwe
Targeted Allele Detail
Summary
Symbol: Sparctm1Hwe
Name: secreted acidic cysteine rich glycoprotein; targeted mutation 1, Chin Chen Howe
MGI ID: MGI:1888383
Synonyms: SP-
Gene: Sparc  Location: Chr11:55284985-55310906 bp, - strand  Genetic Position: Chr11, 33.04 cM, cytoband B1
Alliance: Sparctm1Hwe page
Delayed wound healing in Sparctm1Hwe/Sparctm1Hwe mice

Show the 3 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:52120
Parent Cell Line:  CCE/EK.CCE (ES Cell)
Strain of Origin:  129S/SvEv-Gpi1c
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Insertion
 
Mutation detailsTwo tandem neomycin resistance cassettes were inserted into exon 4. No mRNA was detected by Northern blot in testis, spleen or thymus of homozygous mice. (J:52120)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 9 anatomical structure(s)
Tumor Data
List all tumor models in MMHCdb carrying Sparctm1Hwe
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Sparc Mutation:  75 strains or lines available
References
Original:  J:52120 Norose K, et al., SPARC deficiency leads to early-onset cataractogenesis. Invest Ophthalmol Vis Sci. 1998 Dec;39(13):2674-80
All:  92 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
04/16/2024
MGI 6.23
The Jackson Laboratory