abnormal lung position or orientation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the lung is displaced from the normal position and/or has an altered left/right orientation (Mammalian Phenotype Ontology, MP_0010853)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010853
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Genes

37 gene mutations causing the abnormal lung position or orientation 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
CCDC39 coiled-coil domain containing 39
CCDC40 coiled-coil domain containing 40
CFC1 cripto, FRL-1, cryptic family 1
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
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
DYX1C1 dyslexia susceptibility 1 candidate 1
FOXJ1 forkhead box J1
GDF1 growth differentiation factor 1
HHIP hedgehog interacting protein
HSPB11 heat shock protein family B (small), member 11
IFT140 intraflagellar transport 140
IFT27 intraflagellar transport 27
INVS inversin
LEFTY1 left-right determination factor 1
MEGF8 multiple EGF-like-domains 8
MGRN1 mahogunin ring finger 1, E3 ubiquitin protein ligase
MKS1 Meckel syndrome, type 1
MNS1 meiosis-specific nuclear structural 1
NEK8 NIMA-related kinase 8
NODAL nodal growth differentiation factor
PCSK6 proprotein convertase subtilisin/kexin type 6
PITX2 paired-like homeodomain 2
PKD1L1 polycystic kidney disease 1 like 1
PKD2 polycystic kidney disease 2 (autosomal dominant)
PSKH1 protein serine kinase H1
RPGRIP1L RPGRIP1-like
TBC1D32 TBC1 domain family, member 32
ZIC3 Zic family member 3