abnormal lung compliance Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability of the lung to distend in response to pressure without disruption, usually expressed as the unit volume of change in the lung per unit of pressure (Mammalian Phenotype Ontology, MP_0002333)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002333
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21 gene mutations causing the abnormal lung compliance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
AQP5 aquaporin 5
ATP7A ATPase, Cu++ transporting, alpha polypeptide
CAV1 caveolin 1, caveolae protein, 22kDa
CBY1 chibby homolog 1 (Drosophila)
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
FBN1 fibrillin 1
FUT8 fucosyltransferase 8 (alpha (1,6) fucosyltransferase)
GIT2 G protein-coupled receptor kinase interacting ArfGAP 2
KL klotho
LEPR leptin receptor
LTBP4 latent transforming growth factor beta binding protein 4
NCF1 neutrophil cytosolic factor 1
RAB38 RAB38, member RAS oncogene family
RORA RAR-related orphan receptor A
SEPN1 selenoprotein N, 1
SFTPA1 surfactant protein A1
SFTPB surfactant protein B
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
TLR4 toll-like receptor 4
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B