sacral vertebral transformation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description homeotic transformation of any sacral vertebrae to adopt the fate of another vertebrae (Mammalian Phenotype Ontology, MP_0004617)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004617
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Genes

14 gene mutations causing the sacral vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2B activin A receptor, type IIB
ASXL2 additional sex combs like transcriptional regulator 2
FGFR1 fibroblast growth factor receptor 1
HOXA10 homeobox A10
HOXA11 homeobox A11
HOXC8 homeobox C8
HOXD11 homeobox D11
HOXD9 homeobox D9
KMT2A lysine (K)-specific methyltransferase 2A
NDRG2 NDRG family member 2
PCGF2 polycomb group ring finger 2
RPL38 ribosomal protein L38
WNT3A wingless-type MMTV integration site family, member 3A
ZBTB16 zinc finger and BTB domain containing 16