increased rib number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than normal numbers of the pairs of bony structures that are elements of the body wall (Mammalian Phenotype Ontology, MP_0000480)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000480
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Genes

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

Symbol Name
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
DSCC1 DNA replication and sister chromatid cohesion 1
FGFR1 fibroblast growth factor receptor 1
GDF11 growth differentiation factor 11
GLI2 GLI family zinc finger 2
GSC goosecoid homeobox
HOXA10 homeobox A10
HOXA4 homeobox A4
HOXA5 homeobox A5
HOXA6 homeobox A6
HOXA9 homeobox A9
HOXB9 homeobox B9
HOXC4 homeobox C4
HOXC8 homeobox C8
HOXC9 homeobox C9
HOXD4 homeobox D4
HOXD8 homeobox D8
KAT2A K(lysine) acetyltransferase 2A
KDM7A lysine (K)-specific demethylase 7A
MTF2 metal response element binding transcription factor 2
MYF5 myogenic factor 5
OAS1 2'-5'-oligoadenylate synthetase 1, 40/46kDa
PCSK5 proprotein convertase subtilisin/kexin type 5
PGAP1 post-GPI attachment to proteins 1
PHC2 polyhomeotic homolog 2 (Drosophila)
RING1 ring finger protein 1
RPL38 ribosomal protein L38
RPS7 ribosomal protein S7
SCHIP1 schwannomin interacting protein 1
SCMH1 sex comb on midleg homolog 1 (Drosophila)
SOX11 SRY (sex determining region Y)-box 11
TASP1 taspase, threonine aspartase, 1
TRPS1 trichorhinophalangeal syndrome I
WFIKKN1 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
WNT7A wingless-type MMTV integration site family, member 7A
ZBTB16 zinc finger and BTB domain containing 16