hemolysis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010163
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28 gene mutations causing the hemolysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ADD2 adducin 2 (beta)
AMPD3 adenosine monophosphate deaminase 3
ANK1 ankyrin 1, erythrocytic
AQP9 aquaporin 9
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide
BNIP3L BCL2/adenovirus E1B 19kDa interacting protein 3-like
DMTN dematin actin binding protein
EIF2AK1 eukaryotic translation initiation factor 2-alpha kinase 1
EXOC6 exocyst complex component 6
FECH ferrochelatase
GPI glucose-6-phosphate isomerase
KCNN4 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4
KLF1 Kruppel-like factor 1 (erythroid)
LCAT lecithin-cholesterol acyltransferase
MAN2A1 mannosidase, alpha, class 2A, member 1
NCKAP1L NCK-associated protein 1-like
NEK1 NIMA-related kinase 1
PFKM phosphofructokinase, muscle
PKLR pyruvate kinase, liver and RBC
PPP1R15A protein phosphatase 1, regulatory subunit 15A
PRKAA1 protein kinase, AMP-activated, alpha 1 catalytic subunit
RASA3 RAS p21 protein activator 3
SGMS2 sphingomyelin synthase 2
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic