Jaw Abnormalities Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description any structural anomaly of the bony framework of the mouth where the teeth are held (Mammalian Phenotype Ontology, MP_0000454)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D007569
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8 genes/proteins associated with the disease Jaw Abnormalities from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PCSK5 proprotein convertase subtilisin/kexin type 5 2.88009
TWSG1 twisted gastrulation BMP signaling modulator 1 2.88009
OTX2 orthodenticle homeobox 2 2.88009
SMO smoothened, frizzled class receptor 2.88009
POLD1 polymerase (DNA directed), delta 1, catalytic subunit 2.88009
SHH sonic hedgehog 1.16035
ADH4 alcohol dehydrogenase 4 (class II), pi polypeptide 1.15526
HSPB7 heat shock 27kDa protein family, member 7 (cardiovascular) 1.01286