abnormal mandibule ramus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the upturned perpendicular extremity of the mandible (Mammalian Phenotype Ontology, MP_0010150)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010150
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17 gene mutations causing the abnormal mandibule ramus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CHRD chordin
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
GLI2 GLI family zinc finger 2
GSC goosecoid homeobox
IDUA iduronidase, alpha-L-
NPR2 natriuretic peptide receptor 2
OTX2 orthodenticle homeobox 2
PAX9 paired box 9
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
PTCH1 patched 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
RSPO2 R-spondin 2
TBX1 T-box 1
TGFB2 transforming growth factor, beta 2
ZIC3 Zic family member 3