abnormal left lung morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the organ of respiration located on the left side of the body (Mammalian Phenotype Ontology, MP_0009569)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009569
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17 gene mutations causing the abnormal left lung morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2B activin A receptor, type IIB
ATMIN ATM interactor
C1ORF127 chromosome 1 open reading frame 127
CFC1 cripto, FRL-1, cryptic family 1
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
DNAH11 dynein, axonemal, heavy chain 11
FOXJ1 forkhead box J1
GDF1 growth differentiation factor 1
GLI3 GLI family zinc finger 3
INVS inversin
MEGF8 multiple EGF-like-domains 8
NEK8 NIMA-related kinase 8
NODAL nodal growth differentiation factor
PITX2 paired-like homeodomain 2
PKD1L1 polycystic kidney disease 1 like 1
PKD2 polycystic kidney disease 2 (autosomal dominant)
ZIC3 Zic family member 3