oligodactyly Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect resulting in the presence of fewer than the normal number of digits. (Human Phenotype Ontology, HP_0012165)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000565
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Genes

33 gene mutations causing the oligodactyly phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
CREBBP CREB binding protein
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1
FBXW4 F-box and WD repeat domain containing 4
FGFR1 fibroblast growth factor receptor 1
FMN1 formin 1
FREM2 FRAS1 related extracellular matrix protein 2
GAS1 growth arrest-specific 1
GREM1 gremlin 1, DAN family BMP antagonist
HHAT hedgehog acyltransferase
HOXA13 homeobox A13
HOXD12 homeobox D12
IFT140 intraflagellar transport 140
LMBR1 limb development membrane protein 1
LRP4 low density lipoprotein receptor-related protein 4
LRP6 low density lipoprotein receptor-related protein 6
NABP2 nucleic acid binding protein 2
NCOA6 nuclear receptor coactivator 6
NUBP1 nucleotide binding protein 1
OTOP3 otopetrin 3
PITX1 paired-like homeodomain 1
PORCN porcupine homolog (Drosophila)
PRDM1 PR domain containing 1, with ZNF domain
RFNG RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
RPL38 ribosomal protein L38
RSPO2 R-spondin 2
SALL1 spalt-like transcription factor 1
SHH sonic hedgehog
SP6 Sp6 transcription factor
TBX3 T-box 3
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)
WNT7A wingless-type MMTV integration site family, member 7A
ZBTB16 zinc finger and BTB domain containing 16