| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
