Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3040
Gene Symbol: HBA2
HBA2 		0.460 Biomarker disease HPO
Entrez Id: 3039
Gene Symbol: HBA1
HBA1 		0.160 Biomarker disease HPO
Entrez Id: 164656
Gene Symbol: TMPRSS6
TMPRSS6 		0.110 Biomarker disease HPO
Entrez Id: 51095
Gene Symbol: TRNT1
TRNT1 		0.100 Biomarker disease HPO
Entrez Id: 22
Gene Symbol: ABCB7
ABCB7 		0.100 Biomarker disease HPO
Entrez Id: 3043
Gene Symbol: HBB
HBB 		0.100 Biomarker disease HPO
Entrez Id: 109580095
Gene Symbol: HBB-LCR
HBB-LCR 		0.100 Biomarker disease HPO
Entrez Id: 23729
Gene Symbol: SHPK
SHPK 		0.100 Biomarker disease HPO
Entrez Id: 546
Gene Symbol: ATRX
ATRX 		0.100 Biomarker disease HPO
Entrez Id: 9663
Gene Symbol: LPIN2
LPIN2 		0.100 Biomarker disease HPO
Entrez Id: 212
Gene Symbol: ALAS2
ALAS2 		0.100 Biomarker disease HPO
Entrez Id: 131118
Gene Symbol: DNAJC19
DNAJC19 		0.100 Biomarker disease HPO
Entrez Id: 5367
Gene Symbol: PMCH
PMCH 		0.010 Biomarker disease BEFREE 10.9 g/dL with hypochromic microcytic anemia pattern seen in complete blood count (MCV 70.2 fl, MCH 21.4 pg). 30995913 2019
Entrez Id: 4891
Gene Symbol: SLC11A2
SLC11A2 		0.080 GeneticVariation disease BEFREE Hypochromic microcytic anemia associated with ineffective erythropoiesis caused by recessive mutations in divalent metal transporter 1 (DMT1) can be improved with high-dose erythropoietin supplementation. 22580996 2012
Entrez Id: 3040
Gene Symbol: HBA2
HBA2 		0.460 GeneticVariation disease BEFREE alpha-globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia. 14555321 2003
Entrez Id: 3039
Gene Symbol: HBA1
HBA1 		0.160 GeneticVariation disease BEFREE alpha-globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia. 14555321 2003
Entrez Id: 4891
Gene Symbol: SLC11A2
SLC11A2 		0.080 GeneticVariation disease BEFREE DMT1 mutations are responsible for severe hypochromic microcytic anemia in rodents and in 2 human patients described recently. 16439678 2006
Entrez Id: 25978
Gene Symbol: CHMP2B
CHMP2B 		0.040 GeneticVariation disease BEFREE DMT1 mutations are responsible for severe hypochromic microcytic anemia in rodents and in 2 human patients described recently. 16439678 2006
Entrez Id: 1761
Gene Symbol: DMRT1
DMRT1 		0.040 GeneticVariation disease BEFREE DMT1 mutations are responsible for severe hypochromic microcytic anemia in rodents and in 2 human patients described recently. 16439678 2006
Entrez Id: 4891
Gene Symbol: SLC11A2
SLC11A2 		0.080 Biomarker disease BEFREE DMT1 deficiency must be considered in the differential diagnosis of microcytic hypochromic anemia observed in the newborn period. 18154916 2008
Entrez Id: 25978
Gene Symbol: CHMP2B
CHMP2B 		0.040 Biomarker disease BEFREE DMT1 deficiency must be considered in the differential diagnosis of microcytic hypochromic anemia observed in the newborn period. 18154916 2008
Entrez Id: 1761
Gene Symbol: DMRT1
DMRT1 		0.040 Biomarker disease BEFREE DMT1 deficiency must be considered in the differential diagnosis of microcytic hypochromic anemia observed in the newborn period. 18154916 2008
Entrez Id: 3040
Gene Symbol: HBA2
HBA2 		0.460 GeneticVariation disease BEFREE Alpha-globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran. 31478238 2020
Entrez Id: 3039
Gene Symbol: HBA1
HBA1 		0.160 GeneticVariation disease BEFREE Alpha-globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran. 31478238 2020
Entrez Id: 10661
Gene Symbol: KLF1
KLF1 		0.010 GeneticVariation disease BEFREE Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin. 25585695 2015