pulmonary alveolar hemorrhage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description bleeding into the small sac-like dilations of the distal airspace of the lung (Mammalian Phenotype Ontology, MP_0010909)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010909
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14 gene mutations causing the pulmonary alveolar hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA3 ATP-binding cassette, sub-family A (ABC1), member 3
ATOX1 antioxidant 1 copper chaperone
CHD2 chromodomain helicase DNA binding protein 2
COL1A1 collagen, type I, alpha 1
CRHR1 corticotropin releasing hormone receptor 1
EPHA3 EPH receptor A3
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)
MAN1A2 mannosidase, alpha, class 1A, member 2
NTF3 neurotrophin 3
PLAT plasminogen activator, tissue
PRDX6 peroxiredoxin 6
PTGER4 prostaglandin E receptor 4 (subtype EP4)
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
THBS1 thrombospondin 1