kidney hemorrhage Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	bleeding in the organ of excretion (Mammalian Phenotype Ontology, MP_0000533)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000533
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Genes

13 gene mutations causing the kidney hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
COL2A1	collagen, type II, alpha 1
COL4A3	collagen, type IV, alpha 3 (Goodpasture antigen)
CRIM1	cysteine rich transmembrane BMP regulator 1 (chordin-like)
CXCR4	chemokine (C-X-C motif) receptor 4
FOXC2	forkhead box C2
GNE	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
GPR4	G protein-coupled receptor 4
HNRNPD	heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa)
MAFB	v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
NPHS2	nephrosis 2, idiopathic, steroid-resistant (podocin)
PDGFRB	platelet-derived growth factor receptor, beta polypeptide
PRDX6	peroxiredoxin 6
TNNT3	troponin T type 3 (skeletal, fast)