abnormal metatarsal bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the five bones of the hindpaws/feet that articulate proximally with the cuneiform and cuboid bones of the tarsus and distally with the phalanges (Mammalian Phenotype Ontology, MP_0003072)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003072
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30 gene mutations causing the abnormal metatarsal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
ALKBH1 alkB, alkylation repair homolog 1 (E. coli)
BMPR1B bone morphogenetic protein receptor, type IB
CBFB core-binding factor, beta subunit
CHSY1 chondroitin sulfate synthase 1
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
FGF18 fibroblast growth factor 18
FMN1 formin 1
FOXC1 forkhead box C1
GAS1 growth arrest-specific 1
GDF5 growth differentiation factor 5
GLI3 GLI family zinc finger 3
HOXA13 homeobox A13
HOXD12 homeobox D12
HOXD13 homeobox D13
KIAA1715 KIAA1715
LRP4 low density lipoprotein receptor-related protein 4
MMP9 matrix metallopeptidase 9
NPR3 natriuretic peptide receptor 3
PTH parathyroid hormone
RPL38 ribosomal protein L38
RSPO2 R-spondin 2
SFRP2 secreted frizzled-related protein 2
SMOC1 SPARC related modular calcium binding 1
SP3 Sp3 transcription factor
TBX15 T-box 15
ZBTB16 zinc finger and BTB domain containing 16
ZEB1 zinc finger E-box binding homeobox 1
ZIC2 Zic family member 2