abnormal sternebra number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the average number of the segments of the primordial sternum of the embryo; these segments fuse to form the body of the adult vertebrate sternum (Mammalian Phenotype Ontology, MP_0012282)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012282
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13 gene mutations causing the abnormal sternebra number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CBX2 chromobox homolog 2
HOXA10 homeobox A10
HOXA5 homeobox A5
HOXB7 homeobox B7
HOXB8 homeobox B8
HOXC4 homeobox C4
HOXC8 homeobox C8
KAT2A K(lysine) acetyltransferase 2A
KMT2A lysine (K)-specific methyltransferase 2A
RPL38 ribosomal protein L38
SSBP3 single stranded DNA binding protein 3
TSHZ1 teashirt zinc finger homeobox 1
ZBTB16 zinc finger and BTB domain containing 16