abnormal forelimb stylopod morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the proximal element of the forelimb including the humerus (Mammalian Phenotype Ontology, MP_0003854)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003854
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Genes

65 gene mutations causing the abnormal forelimb stylopod morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACAN aggrecan
AMER1 APC membrane recruitment protein 1
BLZF1 basic leucine zipper nuclear factor 1
BMP5 bone morphogenetic protein 5
BMPER BMP binding endothelial regulator
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CENPJ centromere protein J
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
CSGALNACT1 chondroitin sulfate N-acetylgalactosaminyltransferase 1
DUSP3 dual specificity phosphatase 3
DYM dymeclin
EVC Ellis van Creveld protein
FGF10 fibroblast growth factor 10
FGF9 fibroblast growth factor 9
FGFR3 fibroblast growth factor receptor 3
FOXC1 forkhead box C1
GDF5 growth differentiation factor 5
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
GSC goosecoid homeobox
HOXC8 homeobox C8
HOXD9 homeobox D9
HSPG2 heparan sulfate proteoglycan 2
IFT172 intraflagellar transport 172
IHH indian hedgehog
IL6ST interleukin 6 signal transducer
IMPAD1 inositol monophosphatase domain containing 1
INPP4B inositol polyphosphate-4-phosphatase, type II, 105kDa
LEP leptin
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MMP16 matrix metallopeptidase 16 (membrane-inserted)
NABP2 nucleic acid binding protein 2
NBR1 neighbor of BRCA1 gene 1
NPR2 natriuretic peptide receptor 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
OSTM1 osteopetrosis associated transmembrane protein 1
PAPPA2 pappalysin 2
PAX1 paired box 1
PDS5B PDS5 cohesin associated factor B
PGR progesterone receptor
PHEX phosphate regulating endopeptidase homolog, X-linked
PHOSPHO1 phosphatase, orphan 1
PKDCC protein kinase domain containing, cytoplasmic
POSTN periostin, osteoblast specific factor
PRKG2 protein kinase, cGMP-dependent, type II
PTHLH parathyroid hormone-like hormone
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPL38 ribosomal protein L38
RUNX2 runt-related transcription factor 2
SCX scleraxis basic helix-loop-helix transcription factor
SHH sonic hedgehog
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SOCS2 suppressor of cytokine signaling 2
SOX9 SRY (sex determining region Y)-box 9
SP8 Sp8 transcription factor
TBX15 T-box 15
TGFB2 transforming growth factor, beta 2
TGFBR3 transforming growth factor, beta receptor III
TP63 tumor protein p63
VKORC1 vitamin K epoxide reductase complex, subunit 1
WNT5A wingless-type MMTV integration site family, member 5A
WNT7A wingless-type MMTV integration site family, member 7A
XYLT1 xylosyltransferase I