abnormal carpal bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the nine nodular bones of the joint between the forelimb bones and the front paws/hands consisting of the scapholunar, triangular, greater multiangular, lesser multiangular, capitate, hamate, centrale and the sesamoids (Mammalian Phenotype Ontology, MP_0000554)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000554
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33 gene mutations causing the abnormal carpal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMPR1B bone morphogenetic protein receptor, type IB
CHSY1 chondroitin sulfate synthase 1
COL1A1 collagen, type I, alpha 1
CYP51A1 cytochrome P450, family 51, subfamily A, polypeptide 1
EVX2 even-skipped homeobox 2
FGFR1 fibroblast growth factor receptor 1
FLNB filamin B, beta
FMN1 formin 1
FOXC1 forkhead box C1
GDF5 growth differentiation factor 5
GDF6 growth differentiation factor 6
GLI3 GLI family zinc finger 3
HOXA11 homeobox A11
HOXA13 homeobox A13
HOXD11 homeobox D11
HOXD12 homeobox D12
HOXD13 homeobox D13
IFT88 intraflagellar transport 88
IHH indian hedgehog
KCTD10 potassium channel tetramerization domain containing 10
LMBR1 limb development membrane protein 1
MDGA2 MAM domain containing glycosylphosphatidylinositol anchor 2
NOV nephroblastoma overexpressed
NPR3 natriuretic peptide receptor 3
SALL1 spalt-like transcription factor 1
SALL4 spalt-like transcription factor 4
SLC25A21 solute carrier family 25 (mitochondrial oxoadipate carrier), member 21
SMAD3 SMAD family member 3
TBX3 T-box 3
TBX5 T-box 5
TP63 tumor protein p63
ZEB1 zinc finger E-box binding homeobox 1
ZIC2 Zic family member 2