abnormal supraoccipital bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the bone on the dorsal side of the great foramen of the skull, usually forming a part of the occipital in the adult, but distinct in the young (Mammalian Phenotype Ontology, MP_0000078)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000078
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26 gene mutations causing the abnormal supraoccipital bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
APAF1 apoptotic peptidase activating factor 1
BMPER BMP binding endothelial regulator
CDX1 caudal type homeobox 1
DLX5 distal-less homeobox 5
DMRT2 doublesex and mab-3 related transcription factor 2
FOXC2 forkhead box C2
GBX2 gastrulation brain homeobox 2
GTF2IRD1 GTF2I repeat domain containing 1
HHAT hedgehog acyltransferase
LMX1B LIM homeobox transcription factor 1, beta
MKS1 Meckel syndrome, type 1
MN1 meningioma (disrupted in balanced translocation) 1
MSX2 msh homeobox 2
NKX3-2 NK3 homeobox 2
NPR2 natriuretic peptide receptor 2
PCGF2 polycomb group ring finger 2
PRRX1 paired related homeobox 1
PSIP1 PC4 and SFRS1 interacting protein 1
RUNX2 runt-related transcription factor 2
SCUBE1 signal peptide, CUB domain, EGF-like 1
SP3 Sp3 transcription factor
TBX15 T-box 15
TCF15 transcription factor 15 (basic helix-loop-helix)
WDR19 WD repeat domain 19
WNT9A wingless-type MMTV integration site family, member 9A