anisocytosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally increased variability in the size of erythrocytes. (Human Phenotype Ontology, HP_0011273)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002642
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Genes

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

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
AHSP alpha hemoglobin stabilizing protein
ANK1 ankyrin 1, erythrocytic
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide
BNIP3L BCL2/adenovirus E1B 19kDa interacting protein 3-like
CDK5RAP2 CDK5 regulatory subunit associated protein 2
E2F4 E2F transcription factor 4, p107/p130-binding
EP300 E1A binding protein p300
EPOR erythropoietin receptor
EXOC6 exocyst complex component 6
FECH ferrochelatase
FOXP3 forkhead box P3
GIMAP1-GIMAP5 GIMAP1-GIMAP5 readthrough
HBA1 hemoglobin, alpha 1
HBZ hemoglobin, zeta
HK1 hexokinase 1
HMOX1 heme oxygenase 1
JAK1 Janus kinase 1
JAK2 Janus kinase 2
KLF1 Kruppel-like factor 1 (erythroid)
LIG1 ligase I, DNA, ATP-dependent
MAN2A1 mannosidase, alpha, class 2A, member 1
MIR144 microRNA 144
MIR451A microRNA 451a
NFE2L2 nuclear factor, erythroid 2-like 2
NPM1 nucleophosmin (nucleolar phosphoprotein B23, numatrin)
NPRL3 nitrogen permease regulator-like 3 (S. cerevisiae)
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PRDX1 peroxiredoxin 1
PRKAG1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit
RASA3 RAS p21 protein activator 3
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic
TAL1 T-cell acute lymphocytic leukemia 1
TF transferrin
TTC7A tetratricopeptide repeat domain 7A
UROS uroporphyrinogen III synthase