primary atelectasis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description nonexpansion of the lungs after birth, seen in stillborn organisms and in live born animals that do not establish respiration (Mammalian Phenotype Ontology, MP_0010819)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010819
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Genes

19 gene mutations causing the primary atelectasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA3 ATP-binding cassette, sub-family A (ABC1), member 3
AGRN agrin
ANP32B acidic (leucine-rich) nuclear phosphoprotein 32 family, member B
CLEC1B C-type lectin domain family 1, member B
DPH1 diphthamide biosynthesis 1
FSTL1 follistatin-like 1
HAT1 histone acetyltransferase 1
HHIP hedgehog interacting protein
IGF1 insulin-like growth factor 1 (somatomedin C)
LHX4 LIM homeobox 4
MADD MAP-kinase activating death domain
MNX1 motor neuron and pancreas homeobox 1
NABP2 nucleic acid binding protein 2
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
RC3H1 ring finger and CCCH-type domains 1
SLC32A1 solute carrier family 32 (GABA vesicular transporter), member 1
SNX5 sorting nexin 5
SYK spleen tyrosine kinase
WT1 Wilms tumor 1
Funding