absent supraoccipital bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence 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_0004443)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004443
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Genes

10 gene mutations causing the absent supraoccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
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
NKX3-2 NK3 homeobox 2
PRRX1 paired related homeobox 1
SCUBE1 signal peptide, CUB domain, EGF-like 1
WDR19 WD repeat domain 19