abnormal tarsal bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of any of the eight bones of the instep of the paw/foot: tibiale, talus, calcaneus, navicular, 3 cuneiform, and cuboid bones (Mammalian Phenotype Ontology, MP_0005104)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005104
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31 gene mutations causing the abnormal tarsal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMPR1B bone morphogenetic protein receptor, type IB
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
CREB3L1 cAMP responsive element binding protein 3-like 1
CYP51A1 cytochrome P450, family 51, subfamily A, polypeptide 1
FGFR1 fibroblast growth factor receptor 1
FIGN fidgetin
FMN1 formin 1
FOXC1 forkhead box C1
GDF5 growth differentiation factor 5
GDF6 growth differentiation factor 6
GLCE glucuronic acid epimerase
GLI3 GLI family zinc finger 3
HOXA11 homeobox A11
HOXA13 homeobox A13
HOXD13 homeobox D13
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
IFT88 intraflagellar transport 88
JAG2 jagged 2
NOV nephroblastoma overexpressed
PITX1 paired-like homeodomain 1
PLAGL1 pleiomorphic adenoma gene-like 1
RAB23 RAB23, member RAS oncogene family
SHH sonic hedgehog
SMAD3 SMAD family member 3
SOX11 SRY (sex determining region Y)-box 11
SOX8 SRY (sex determining region Y)-box 8
TBX3 T-box 3
TBX4 T-box 4
ZBTB16 zinc finger and BTB domain containing 16
ZEB1 zinc finger E-box binding homeobox 1
ZIC2 Zic family member 2