tracheal stenosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002777
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Genes

23 genes associated with the tracheal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTSL2 ADAMTS-like 2
COL2A1 collagen, type II, alpha 1
DHCR7 7-dehydrocholesterol reductase
EBP emopamil binding protein (sterol isomerase)
FBN1 fibrillin 1
FLNA filamin A, alpha
FLNB filamin B, beta
FOXI1 forkhead box I1
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
HOXD13 homeobox D13
HYLS1 hydrolethalus syndrome 1
IDUA iduronidase, alpha-L-
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KIF7 kinesin family member 7
MGP matrix Gla protein
PCNT pericentrin
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SMAD4 SMAD family member 4
WNT3 wingless-type MMTV integration site family, member 3