abnormal interparietal bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the bone of the cranium that lies above and anterior to the occipital bone in some mammals (Mammalian Phenotype Ontology, MP_0000077)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000077
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Genes

44 gene mutations causing the abnormal interparietal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALKBH1 alkB, alkylation repair homolog 1 (E. coli)
ALX1 ALX homeobox 1
APAF1 apoptotic peptidase activating factor 1
BMP1 bone morphogenetic protein 1
BMPER BMP binding endothelial regulator
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CHUK conserved helix-loop-helix ubiquitous kinase
DKK1 dickkopf WNT signaling pathway inhibitor 1
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
GJA1 gap junction protein, alpha 1, 43kDa
GTF2IRD1 GTF2I repeat domain containing 1
HECTD1 HECT domain containing E3 ubiquitin protein ligase 1
HHAT hedgehog acyltransferase
HOXA1 homeobox A1
LMX1A LIM homeobox transcription factor 1, alpha
LMX1B LIM homeobox transcription factor 1, beta
MBTD1 mbt domain containing 1
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MN1 meningioma (disrupted in balanced translocation) 1
MNT MAX network transcriptional repressor
MSX2 msh homeobox 2
NELL1 NEL-like 1 (chicken)
NOG noggin
NPR2 natriuretic peptide receptor 2
PEX2 peroxisomal biogenesis factor 2
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
PSIP1 PC4 and SFRS1 interacting protein 1
PTCH1 patched 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
RUNX2 runt-related transcription factor 2
SC5D sterol-C5-desaturase
SCUBE1 signal peptide, CUB domain, EGF-like 1
SHH sonic hedgehog
SKI SKI proto-oncogene
SP3 Sp3 transcription factor
TCOF1 Treacher Collins-Franceschetti syndrome 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TGFB2 transforming growth factor, beta 2
TWIST1 twist family bHLH transcription factor 1
WDR19 WD repeat domain 19