decreased presacral vertebrae number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced number of the vertebrae anterior to the sacrum (Mammalian Phenotype Ontology, MP_0000461)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000461
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Genes

31 gene mutations causing the decreased presacral 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
FAM134C family with sequence similarity 134, member C
FST follistatin
HOXD11 homeobox D11
JMJD1C jumonji domain containing 1C
KAT2A K(lysine) acetyltransferase 2A
KAT6A K(lysine) acetyltransferase 6A
LASP1 LIM and SH3 protein 1
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MLLT3 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3
MTA1 metastasis associated 1
NACC1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing
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)
T T, brachyury homolog (mouse)
TM9SF4 transmembrane 9 superfamily protein member 4
UBA2 ubiquitin-like modifier activating enzyme 2
WNT3A wingless-type MMTV integration site family, member 3A
WNT7A wingless-type MMTV integration site family, member 7A
ZC3HC1 zinc finger, C3HC-type containing 1