increased vertebrae number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004644
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Genes

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

Symbol Name
ACVR2B activin A receptor, type IIB
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
GDF11 growth differentiation factor 11
HOXA10 homeobox A10
HOXA11 homeobox A11
HOXD11 homeobox D11
JMJD1C jumonji domain containing 1C
KDM7A lysine (K)-specific demethylase 7A
MTA1 metastasis associated 1
MYSM1 Myb-like, SWIRM and MPN domains 1
NPR3 natriuretic peptide receptor 3
OAS1 2'-5'-oligoadenylate synthetase 1, 40/46kDa
PCSK5 proprotein convertase subtilisin/kexin type 5
RPL24 ribosomal protein L24
RPL38 ribosomal protein L38
SLC44A5 solute carrier family 44, member 5
SLX4 SLX4 structure-specific endonuclease subunit
SPNS2 spinster homolog 2 (Drosophila)
TM9SF4 transmembrane 9 superfamily protein member 4
UBA2 ubiquitin-like modifier activating enzyme 2
XPNPEP1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble
ZBTB16 zinc finger and BTB domain containing 16