abnormal basioccipital bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the basilar process of the occipital bone in the base of the cranium, frequently forming a direct part of the occipital in the adult, but usually distinct in the young (Mammalian Phenotype Ontology, MP_0000079)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000079
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Genes

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

Symbol Name
ANKH ANKH inorganic pyrophosphate transport regulator
BMP7 bone morphogenetic protein 7
CDX1 caudal type homeobox 1
CHRD chordin
DLX5 distal-less homeobox 5
EVC Ellis van Creveld protein
FGFRL1 fibroblast growth factor receptor-like 1
GLI2 GLI family zinc finger 2
HHAT hedgehog acyltransferase
HOXA1 homeobox A1
HOXA2 homeobox A2
HOXD4 homeobox D4
LTBP1 latent transforming growth factor beta binding protein 1
LTBP3 latent transforming growth factor beta binding protein 3
NKX3-2 NK3 homeobox 2
PSEN1 presenilin 1
RARB retinoic acid receptor, beta
RARG retinoic acid receptor, gamma
SKI SKI proto-oncogene
TBX1 T-box 1
TBX15 T-box 15
TCF15 transcription factor 15 (basic helix-loop-helix)
TMEM107 transmembrane protein 107
WNT9A wingless-type MMTV integration site family, member 9A