Craniofacial Asymmetry Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Asymmetry of the bones of the skull and the face. (Human Phenotype Ontology, HP_0004484)
External Link https://www.disgenet.org/browser/0/1/0/C4025320
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Genes

15 genes associated with the disease Craniofacial Asymmetry in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ANXA1 annexin A1
CDCA5 cell division cycle associated 5
CDK5R1 cyclin-dependent kinase 5, regulatory subunit 1 (p35)
CPLX1 complexin 1
CTBP1 C-terminal binding protein 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
ESR1 estrogen receptor 1
FCN2 ficolin (collagen/fibrinogen domain containing lectin) 2
FGFRL1 fibroblast growth factor receptor-like 1
GCHFR GTP cyclohydrolase I feedback regulator
IL12A interleukin 12A
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
LOC105375355 uroplakin-3b
MNAT1 MNAT CDK-activating kinase assembly factor 1
NSD2 nuclear receptor binding SET domain protein 2