abnormal metacarpal 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 forepaws/hands that articulate proximally with the carpal bones and distally with the phalanges (Mammalian Phenotype Ontology, MP_0003073)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003073
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33 gene mutations causing the abnormal metacarpal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMPR1B bone morphogenetic protein receptor, type IB
CBFB core-binding factor, beta subunit
CHSY1 chondroitin sulfate synthase 1
EVX2 even-skipped homeobox 2
FBN1 fibrillin 1
FMN1 formin 1
FOXC1 forkhead box C1
FSTL1 follistatin-like 1
GAS1 growth arrest-specific 1
GDF5 growth differentiation factor 5
GLI3 GLI family zinc finger 3
GREM1 gremlin 1, DAN family BMP antagonist
HOXA13 homeobox A13
HOXD11 homeobox D11
HOXD12 homeobox D12
HOXD13 homeobox D13
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
KIAA1715 KIAA1715
LIFR leukemia inhibitory factor receptor alpha
LRP4 low density lipoprotein receptor-related protein 4
NPR3 natriuretic peptide receptor 3
PRRX1 paired related homeobox 1
PTH parathyroid hormone
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPL38 ribosomal protein L38
SALL1 spalt-like transcription factor 1
SALL4 spalt-like transcription factor 4
SFRP2 secreted frizzled-related protein 2
SHH sonic hedgehog
SP3 Sp3 transcription factor
TBX15 T-box 15
TBX3 T-box 3
ZIC2 Zic family member 2