decreased lumbar vertebrae number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced number of the six bony segments of the spine located anterior to the sacral vertebrae and posterior to the thoracic vertebrae (Mammalian Phenotype Ontology, MP_0004647)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004647
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Genes

23 gene mutations causing the decreased lumbar vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
BMP7 bone morphogenetic protein 7
BRDT bromodomain, testis-specific
CBX5 chromobox homolog 5
DLL1 delta-like 1 (Drosophila)
DSCC1 DNA replication and sister chromatid cohesion 1
EFNA1 ephrin-A1
ESCO1 establishment of sister chromatid cohesion N-acetyltransferase 1
FST follistatin
HOXD11 homeobox D11
JMJD1C jumonji domain containing 1C
KAT2A K(lysine) acetyltransferase 2A
LASP1 LIM and SH3 protein 1
MTA1 metastasis associated 1
NOTO notochord homeobox
NRARP NOTCH-regulated ankyrin repeat protein
PPP5C protein phosphatase 5, catalytic subunit
PSIP1 PC4 and SFRS1 interacting protein 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
WNT3A wingless-type MMTV integration site family, member 3A