abnormal branching involved in lung morphogenesis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process in which the branched structure of the respiratory airway tree is generated and organized (Mammalian Phenotype Ontology, MP_0011024)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011024
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26 gene mutations causing the abnormal branching involved in lung morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
BAG6 BCL2-associated athanogene 6
BMPER BMP binding endothelial regulator
CELSR1 cadherin, EGF LAG seven-pass G-type receptor 1
EGFR epidermal growth factor receptor
FGF10 fibroblast growth factor 10
FGF9 fibroblast growth factor 9
FGFR2 fibroblast growth factor receptor 2
HOXA5 homeobox A5
IGF2R insulin-like growth factor 2 receptor
ITGA3 integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor)
ITGA8 integrin, alpha 8
LOX lysyl oxidase
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NFIB nuclear factor I/B
NKX2-1 NK2 homeobox 1
NPAS3 neuronal PAS domain protein 3
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NUBP1 nucleotide binding protein 1
RDH10 retinol dehydrogenase 10 (all-trans)
SHH sonic hedgehog
STK11 serine/threonine kinase 11
TCF21 transcription factor 21
TIMP3 TIMP metallopeptidase inhibitor 3
TMTC3 transmembrane and tetratricopeptide repeat containing 3
VANGL2 VANGL planar cell polarity protein 2