hematuria Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description The presence of blood in the urine. Hematuria may be gross hematuria (visible to the naked eye) or microscopic hematuria (detected by dipstick or microscopic examination of the urine). (Human Phenotype Ontology, HP_0000790)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005161
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Genes

12 gene mutations causing the hematuria phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CFH complement factor H
CLU clusterin
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
DDR1 discoidin domain receptor tyrosine kinase 1
LAMA5 laminin, alpha 5
MAN2A1 mannosidase, alpha, class 2A, member 1
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
MYH9 myosin, heavy chain 9, non-muscle
MYO1E myosin IE
SCARF1 scavenger receptor class F, member 1
TXNIP thioredoxin interacting protein