increased sacral vertebrae number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase of any or all of the bony segments of the spine located posterior to the lumbar vertebrae and anterior to the caudal vertebrae (Mammalian Phenotype Ontology, MP_0010101)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010101
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Genes

15 gene mutations causing the increased sacral vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
BRDT bromodomain, testis-specific
CBX5 chromobox homolog 5
CENPJ centromere protein J
DSCC1 DNA replication and sister chromatid cohesion 1
DUSP4 dual specificity phosphatase 4
EFNA1 ephrin-A1
ESCO1 establishment of sister chromatid cohesion N-acetyltransferase 1
JMJD1C jumonji domain containing 1C
MTA1 metastasis associated 1
MYSM1 Myb-like, SWIRM and MPN domains 1
SLC44A5 solute carrier family 44, member 5
SPNS2 spinster homolog 2 (Drosophila)
TM9SF4 transmembrane 9 superfamily protein member 4
UBA2 ubiquitin-like modifier activating enzyme 2