GeneSet Information

Tier II GS135915 • gestational survival modifier locus (Gstml, Published QTL Chr 2)

DESCRIPTION:

QTL associated with gestational survival modifier locus. This interval was obtained by using a fixed interval width of 25 Mbp around the peak marker (155950416)

LABEL:

QTL-Gstml-Mouse-Chr 2

SCORE TYPE:

Binary

DATE ADDED:

2012-04-02

DATE UPDATED:

2020-05-06

SPECIES:

AUTHORS:

Leder A, McMenamin J, Fontaine K, Bishop A, Leder P

TITLE:

zeta-/- Thalassemic mice are affected by two modifying loci and display unanticipated somatic recombination leading to inherited variation.

JOURNAL:

Human molecular genetics Mar 2005, Vol 14, pp. 615-25

ABSTRACT:

Thalassemia is a disease caused by a variety of mutations affecting both the adult and embryonic alpha- and beta-globin loci. A mouse strain carrying an embryonic zeta-globin gene disrupted by the insertion of a PGK-Neo cassette displays an alpha-thalassemia-like syndrome. Embryonic survival of this zeta-null mouse is variable and strongly influenced by genetic background, the 129/SvEv mouse strain displaying a more severe phenotype than C57BL/6. We have identified two modifying loci on C57BL/6 chromosomes 2 and 5, which affect the penetrance of embryonic lethality in the 129/SvEv mouse. Through this work, we were able to observe an interesting effect on somatic recombination events in thalassemic embryos. We show that these events can occur on multiple chromosomes in very early embryonic cells, prior to their allocation to the germline. Our results demonstrate that somatic recombination events can be transmitted to subsequent generations. PUBMED: 15649944
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Annotation Information

No sequence read archive data associated with this GeneSet.


Family Characteristics (D005191)
Chromosomes (D002875)
Thalassemia (D013789)
Recombination, Genetic (D011995)
Embryonic Structures (D004628)
beta-Globins (D055544)
zeta-Globins (D055543)
Lifting (D017770)
Survival (D013534)
Mutation (D009154)
Penetrance (D019683)
embryonic lethality (MP:0008762)

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