anemia of inadequate production Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A kind of anemia characterized by inadequate production of erythrocytes. (Human Phenotype Ontology, HP_0010972)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010972
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Genes

79 genes associated with the anemia of inadequate production phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7
ACVRL1 activin A receptor type II-like 1
AGGF1 angiogenic factor with G patch and FHA domains 1
ALAS2 5'-aminolevulinate synthase 2
ALDOA aldolase A, fructose-bisphosphate
AMN amnion associated transmembrane protein
ANKRD11 ankyrin repeat domain 11
ATRX alpha thalassemia/mental retardation syndrome X-linked
BPGM 2,3-bisphosphoglycerate mutase
C15ORF41 chromosome 15 open reading frame 41
CASP10 caspase 10, apoptosis-related cysteine peptidase
CDAN1 codanin 1
COX4I2 cytochrome c oxidase subunit IV isoform 2 (lung)
CUBN cubilin (intrinsic factor-cobalamin receptor)
DHFR dihydrofolate reductase
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
ENG endoglin
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
FECH ferrochelatase
FTCD formimidoyltransferase cyclodeaminase
GATA1 GATA binding protein 1 (globin transcription factor 1)
GDF2 growth differentiation factor 2
GIF gastric intrinsic factor (vitamin B synthesis)
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
HBD hemoglobin, delta
HBG1 hemoglobin, gamma A
HK1 hexokinase 1
HPRT1 hypoxanthine phosphoribosyltransferase 1
IRX5 iroquois homeobox 5
ISCU iron-sulfur cluster assembly enzyme
KLF1 Kruppel-like factor 1 (erythroid)
LCAT lecithin-cholesterol acyltransferase
LCRB locus control region, beta
LMBRD1 LMBR1 domain containing 1
LPIN2 lipin 2
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MVK mevalonate kinase
MYD88 myeloid differentiation primary response 88
PHGDH phosphoglycerate dehydrogenase
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
PUS1 pseudouridylate synthase 1
RMRP RNA component of mitochondrial RNA processing endoribonuclease
RPL11 ribosomal protein L11
RPL15 ribosomal protein L15
RPL26 ribosomal protein L26
RPL35A ribosomal protein L35a
RPL5 ribosomal protein L5
RPS10 ribosomal protein S10
RPS14 ribosomal protein S14
RPS17 ribosomal protein S17
RPS19 ribosomal protein S19
RPS24 ribosomal protein S24
RPS26 ribosomal protein S26
RPS29 ribosomal protein S29
RPS7 ribosomal protein S7
SBDS Shwachman-Bodian-Diamond syndrome
SEC23B Sec23 homolog B (S. cerevisiae)
SFXN4 sideroflexin 4
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
SLC46A1 solute carrier family 46 (folate transporter), member 1
SMAD4 SMAD family member 4
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal
SRD5A3 steroid 5 alpha-reductase 3
STK11 serine/threonine kinase 11
TCN2 transcobalamin II
TF transferrin
TMPRSS6 transmembrane protease, serine 6
TPI1 triosephosphate isomerase 1
UMPS uridine monophosphate synthetase
WAS Wiskott-Aldrich syndrome
WFS1 Wolfram syndrome 1 (wolframin)
WIPF1 WAS/WASL interacting protein family, member 1
YARS2 tyrosyl-tRNA synthetase 2, mitochondrial