abnormal right lung morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the part of the organ of respiration located on the right side of the body and consists of the caudal, cranial, middle and accessory lobes (Mammalian Phenotype Ontology, MP_0009570)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009570
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Genes

33 gene mutations causing the abnormal right lung morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATMIN ATM interactor
CCDC39 coiled-coil domain containing 39
CCDC40 coiled-coil domain containing 40
DAND5 DAN domain family member 5, BMP antagonist
DAW1 dynein assembly factor with WDR repeat domains 1
DNAAF3 dynein, axonemal, assembly factor 3
DNAH11 dynein, axonemal, heavy chain 11
DNAH5 dynein, axonemal, heavy chain 5
DNAI1 dynein, axonemal, intermediate chain 1
DRC1 dynein regulatory complex subunit 1
FGFR2 fibroblast growth factor receptor 2
FOXF1 forkhead box F1
FRAS1 Fraser extracellular matrix complex subunit 1
FREM1 FRAS1 related extracellular matrix 1
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
HHIP hedgehog interacting protein
HSPB11 heat shock protein family B (small), member 11
IFT140 intraflagellar transport 140
INVS inversin
ITGA8 integrin, alpha 8
LAMA5 laminin, alpha 5
LEFTY1 left-right determination factor 1
MGRN1 mahogunin ring finger 1, E3 ubiquitin protein ligase
MKS1 Meckel syndrome, type 1
MNS1 meiosis-specific nuclear structural 1
NOG noggin
PCSK6 proprotein convertase subtilisin/kexin type 6
PKD2 polycystic kidney disease 2 (autosomal dominant)
RPGRIP1L RPGRIP1-like
TBC1D32 TBC1 domain family, member 32
ZFPM2 zinc finger protein, FOG family member 2
ZIC3 Zic family member 3