About   Help   FAQ
Phenotype Image Detail
Image
Caption Loss of Sestd1 causes a spectrum of posterior defects that phenocopies loss of Dact1. A, Sestd1tm1.1Bnrc/Sestd1tm1.1Bnrc (Sestd1-/-) phenocopies Dact1tm1.1Bnrc/Dact1tm1.1Bnrc (Dact1-/-) in mice. Sestd1tm1.1Bnrc/Sestd1tm1.1Bnrc mutants (mut) die before or within 1 day of birth, and at postnatal day 0 they have a short tail (arrow). B, Sestd1-/- mutant neonates lack genital tubercle (gt) and anus (a) (filled arrowhead and empty arrowhead). Some Sestd1-/- mutant neonates also have spina bifida (SB) and curled tails. C, Sestd1-/- mutant neonates have blind-ended colons (cn). D, Sestd1-/- mutant neonates have hydronephrotic horseshoe kidneys (hk) and no bladder (b). Scale bar, 500 um. Other abbreviations: wt, wild-type; mut, Sestd1 mutant; c, cecum; k, kidney; hn, hydronephrosis.
Copyright This image is from Yang X, J Biol Chem 2013 Jul 12;288(28):20111-20 and is displayed with the permission of the American Society for Biochemistry and Molecular Biology who owns the Copyright. Full text from JBC. J:201925
Associated
Alleles
Symbol Name
Dact1tm1.1Bnrc dishevelled-binding antagonist of beta-catenin 1; targeted mutation 1.1, Benjamin N R Cheyette
Sestd1tm1.1Bnrc SEC14 and spectrin domains 1; targeted mutation 1.1, Benjamin Cheyette
Associated
Genotypes
Allelic Composition Genetic Background
Dact1tm1.1Bnrc/Dact1tm1.1Bnrc involves: 129
Sestd1tm1.1Bnrc/Sestd1tm1.1Bnrc involves: 129S6/SvEvTac * C57BL/6NCr

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
04/16/2024
MGI 6.23
The Jackson Laboratory