abnormal thyroid cartilage morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the largest of the laryngeal cartilages (Mammalian Phenotype Ontology, MP_0002260)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002260
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Genes

18 gene mutations causing the abnormal thyroid cartilage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
BMP5 bone morphogenetic protein 5
BMP7 bone morphogenetic protein 7
BMPER BMP binding endothelial regulator
CHRD chordin
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
EYA1 EYA transcriptional coactivator and phosphatase 1
FBLN1 fibulin 1
FGFRL1 fibroblast growth factor receptor-like 1
FOXC1 forkhead box C1
HOXA3 homeobox A3
PAX9 paired box 9
PKD1 polycystic kidney disease 1 (autosomal dominant)
RAI1 retinoic acid induced 1
RARA retinoic acid receptor, alpha
SATB2 SATB homeobox 2
TBX1 T-box 1
Funding