Tracheomalacia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A tracheal disease characterized by flaccidity of the tracheal support cartilage. (Human Disease Ontology, DOID_0060313)
External Link https://www.disgenet.org/browser/0/1/0/C0948187
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Genes

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

Symbol Name
ACTL6B actin-like 6B
AMER1 APC membrane recruitment protein 1
ANO1 anoctamin 1, calcium activated chloride channel
BMPER BMP binding endothelial regulator
COL2A1 collagen, type II, alpha 1
DCHS1 dachsous cadherin-related 1
ERF Ets2 repressor factor
FAT4 FAT atypical cadherin 4
FBN2 fibrillin 2
FGFR2 fibroblast growth factor receptor 2
FLNB filamin B, beta
FN1 fibronectin 1
GMNN geminin, DNA replication inhibitor
GNAS GNAS complex locus
H3F3A H3 histone, family 3A
HDAC4 histone deacetylase 4
HRAS Harvey rat sarcoma viral oncogene homolog
IL10 interleukin 10
LTBP4 latent transforming growth factor beta binding protein 4
MMRN1 multimerin 1
OPHN1 oligophrenin 1
ORC4 origin recognition complex, subunit 4
ORC6 origin recognition complex, subunit 6
PAX3 paired box 3
PRRX1 paired related homeobox 1
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
RPL5 ribosomal protein L5
SNRPB small nuclear ribonucleoprotein polypeptides B and B1
SOX9 SRY (sex determining region Y)-box 9
TRIM2 tripartite motif containing 2