abnormal fontanelle morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the membranous interval at the margins of cranial bones in neonates (Mammalian Phenotype Ontology, MP_0000084)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000084
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Genes

18 gene mutations causing the abnormal fontanelle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATF4 activating transcription factor 4
ATR ATR serine/threonine kinase
BNC2 basonuclin 2
CREBBP CREB binding protein
CTSK cathepsin K
DLX5 distal-less homeobox 5
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
LMX1B LIM homeobox transcription factor 1, beta
MKS1 Meckel syndrome, type 1
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MSX1 msh homeobox 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
RUNX2 runt-related transcription factor 2
SIK3 SIK family kinase 3
TFPI tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)
TGFB2 transforming growth factor, beta 2
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta