Congenital Hypoplasia Of Clavicle Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0426799
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Genes

28 genes associated with the disease Congenital Hypoplasia Of Clavicle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide
B4GALT7 xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
BCOR BCL6 corepressor
BGN biglycan
DCHS1 dachsous cadherin-related 1
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
FAT4 FAT atypical cadherin 4
FBXL3 F-box and leucine-rich repeat protein 3
FGFR2 fibroblast growth factor receptor 2
FIG4 FIG4 phosphoinositide 5-phosphatase
FLNA filamin A, alpha
HOXD13 homeobox D13
IDUA iduronidase, alpha-L-
LMNA lamin A/C
MSX2 msh homeobox 2
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
PIN1 peptidylprolyl cis/trans isomerase, NIMA-interacting 1
PORCN porcupine homolog (Drosophila)
RPTOR regulatory associated protein of MTOR, complex 1
RSPO2 R-spondin 2
RUNX2 runt-related transcription factor 2
SRCAP Snf2-related CREBBP activator protein
TBX3 T-box 3
TBX5 T-box 5
TRIP11 thyroid hormone receptor interactor 11
TWIST1 twist family bHLH transcription factor 1
XYLT1 xylosyltransferase I
ZMPSTE24 zinc metallopeptidase STE24