abnormal nasal cavity morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the portion of the respiratory tract that extends from the nares to the pharynx; the nasal cavity is lined with ciliated mucosa (Mammalian Phenotype Ontology, MP_0002237)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002237
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17 gene mutations causing the abnormal nasal cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A3 aldehyde dehydrogenase 1 family, member A3
COL2A1 collagen, type II, alpha 1
DHCR7 7-dehydrocholesterol reductase
E2F4 E2F transcription factor 4, p107/p130-binding
EDA ectodysplasin A
GLI3 GLI family zinc finger 3
GSC goosecoid homeobox
HESX1 HESX homeobox 1
HHAT hedgehog acyltransferase
OTX2 orthodenticle homeobox 2
PAX6 paired box 6
RPL38 ribosomal protein L38
SFN stratifin
SIX1 SIX homeobox 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
ZEB1 zinc finger E-box binding homeobox 1
ZNF423 zinc finger protein 423