absent caudal vertebrae Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of all of the bony segments of the coccyx or tail (Mammalian Phenotype Ontology, MP_0004653)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004653
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7 gene mutations causing the absent caudal vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACAN aggrecan
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
PCSK5 proprotein convertase subtilisin/kexin type 5
RPL38 ribosomal protein L38
SP8 Sp8 transcription factor
TACC3 transforming, acidic coiled-coil containing protein 3
WNT5A wingless-type MMTV integration site family, member 5A