abnormal forelimb zeugopod morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the distal elements of the forelimb including the radius and ulna (Mammalian Phenotype Ontology, MP_0003855)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003855
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Genes

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

Symbol Name
AMER1 APC membrane recruitment protein 1
ANO6 anoctamin 6
BMP5 bone morphogenetic protein 5
CENPJ centromere protein J
CHKB choline kinase beta
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
CREB3L1 cAMP responsive element binding protein 3-like 1
CTGF connective tissue growth factor
CYP51A1 cytochrome P450, family 51, subfamily A, polypeptide 1
EGR2 early growth response 2
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
EVX2 even-skipped homeobox 2
FBN1 fibrillin 1
FGF10 fibroblast growth factor 10
FGF18 fibroblast growth factor 18
FGF9 fibroblast growth factor 9
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
FMN1 formin 1
FOXC1 forkhead box C1
GDF5 growth differentiation factor 5
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
HOXA11 homeobox A11
HOXD11 homeobox D11
HOXD12 homeobox D12
HOXD13 homeobox D13
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
KCTD10 potassium channel tetramerization domain containing 10
KIAA1715 KIAA1715
LGI4 leucine-rich repeat LGI family, member 4
LMX1B LIM homeobox transcription factor 1, beta
LTBP1 latent transforming growth factor beta binding protein 1
NABP2 nucleic acid binding protein 2
NPR2 natriuretic peptide receptor 2
OFD1 oral-facial-digital syndrome 1
PAPPA2 pappalysin 2
PDS5B PDS5 cohesin associated factor B
PHEX phosphate regulating endopeptidase homolog, X-linked
PHOSPHO1 phosphatase, orphan 1
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKDCC protein kinase domain containing, cytoplasmic
POSTN periostin, osteoblast specific factor
PRKG2 protein kinase, cGMP-dependent, type II
PRRX1 paired related homeobox 1
PTHLH parathyroid hormone-like hormone
RAB23 RAB23, member RAS oncogene family
RDH10 retinol dehydrogenase 10 (all-trans)
RECK reversion-inducing-cysteine-rich protein with kazal motifs
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPL38 ribosomal protein L38
RSPO2 R-spondin 2
RUNX2 runt-related transcription factor 2
RYK receptor-like tyrosine kinase
SC5D sterol-C5-desaturase
SFN stratifin
SFRP2 secreted frizzled-related protein 2
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
TBX3 T-box 3
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TGFB2 transforming growth factor, beta 2
THRA thyroid hormone receptor, alpha
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
ZEB1 zinc finger E-box binding homeobox 1