schistocytosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an abnormal number of fragmented red blood cells (schistocytes) in the blood. (Human Phenotype Ontology, HP_0001981)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000314
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Genes

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

Symbol Name
ANK1 ankyrin 1, erythrocytic
CD59 CD59 molecule, complement regulatory protein
NCKAP1L NCK-associated protein 1-like
NFE2L2 nuclear factor, erythroid 2-like 2
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PRDX2 peroxiredoxin 2
SLC20A1 solute carrier family 20 (phosphate transporter), member 1
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic