abnormal tracheal cartilage morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the cartilaginous structures that support the trachea (Mammalian Phenotype Ontology, MP_0003120)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003120
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24 gene mutations causing the abnormal tracheal cartilage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACAN aggrecan
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
ANO1 anoctamin 1, calcium activated chloride channel
ARSB arylsulfatase B
BMPER BMP binding endothelial regulator
CACNA1H calcium channel, voltage-dependent, T type, alpha 1H subunit
COL11A1 collagen, type XI, alpha 1
FBN1 fibrillin 1
FGFR2 fibroblast growth factor receptor 2
FOXC1 forkhead box C1
FSTL1 follistatin-like 1
GLI2 GLI family zinc finger 2
HOXA5 homeobox A5
KL klotho
MGP matrix Gla protein
NKX2-1 NK2 homeobox 1
RARA retinoic acid receptor, alpha
RARG retinoic acid receptor, gamma
RSPO2 R-spondin 2
SHH sonic hedgehog
SOX9 SRY (sex determining region Y)-box 9
TRAF4 TNF receptor-associated factor 4
TRPS1 trichorhinophalangeal syndrome I
WNT5A wingless-type MMTV integration site family, member 5A