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Hmga2pg-Tg40ACha
Transgenic Allele Detail
Summary
Symbol: Hmga2pg-Tg40ACha
Name: high mobility group AT-hook 2; isoform C transgenic, nonhomologous insert 40A, Kiran Chada
MGI ID: MGI:1858044
Gene: Hmga2  Location: Chr10:120197180-120312374 bp, - strand  Genetic Position: Chr10, 67.94 cM
Alliance: Hmga2pg-Tg40ACha page
Transgene
origin
Strain of Origin:  (CBA/J x C57BL/6J)F1
Transgene
description
Transgene Type:    Transgenic
Mutations:    Deletion, Insertion
  Hmga2pg-Tg40ACha involves 1 genes/genome features (Hmga2) View all
 
Mutation detailsA human globin gene transgene caused this insertional mutation shown to be allelic to Hmga2 and determined to comprise a deletion that included the high mobility group protein I, isoform C (Hmga2) gene. (J:28571, J:74548)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 4 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Hmga2 Mutation:  12 strains or lines available
References
Original:  J:10325 Xiang X, et al., Mini-mouse: disruption of the pygmy locus in a transgenic insertional mutant. Science. 1990 Feb 23;247(4945):967-9
All:  5 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
11/12/2024
MGI 6.24
The Jackson Laboratory