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Gene Expression Data
Assay Details
Assay
Reference: J:71694 Bruneau S, et al., The mouse hoxd13(spdh) mutation, a polyalanine expansion similar to human type ii synpolydactyly (spd), disrupts the function but not the expression of other hoxd genes. Dev Biol. 2001 Sep 15;237(2):345-53
Assay type: RNA in situ
MGI Accession ID: MGI:2153101
Gene symbol: Hoxd12
Gene name: homeobox D12
Results
Specimen 3I, +/+: embryonic day 11.5 (more )
Structure Level Pattern Image Note
TS19: limb Present 3I Hoxd12 left
Specimen 3I, -/-: embryonic day 11.5; Hoxd13spdh/Hoxd13spdh (more )
Structure Level Pattern Image Note
TS19: limb Present 3I Hoxd12 right Expression in this mutant is the same as in wild-type embryos.
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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05/07/2024
MGI 6.23 		The Jackson Laboratory