hereditary elliptocytosis Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present. (Human Disease Ontology, DOID_2373)
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7 genes involed in the disease hereditary elliptocytosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ACSL4 acyl-CoA synthetase long-chain family member 4
ANK1 ankyrin 1, erythrocytic
EPB41 erythrocyte membrane protein band 4.1
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic