GYPA - glycophorin A (MNS blood group) Gene

Also Known as MN; GPA; MNS; GPSAT; PAS-2; CD235a; GPErik; HGpMiV; HGpMiXI; HGpSta(C)

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 2993

About GYPA

Cytogenetic location: 4q31.21 Genomic coordinates (GRCh38): 4:144,109,303-144,140,718 (from NCBI)

This gene has 20 transcripts (splice variants), 35 orthologues, 2 paralogues and is associated with 2 phenotypes. Restricted expression toward bone marrow (RPKM 31.9).

Summary

Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups. In addition to the M or N and S or s antigens that commonly occur in all populations, about 40 related variant phenotypes have been identified. These variants include all the variants of the Miltenberger complex and several isoforms of Sta, as well as Dantu, Sat, He, Mg, and deletion variants Ena, S-s-U- and Mk. Most of the variants are the result of gene recombinations between GYPA and GYPB. [provided by RefSeq, Jul 2008]

GYPA Products (3)

mRNA Protein Name
NM_001308187.2 NP_001295116.1 glycophorin-A isoform 2 precursor
NM_001308190.2 NP_001295119.1 glycophorin-A isoform 3
NM_002099.8 NP_002090.4 glycophorin-A isoform 1 precursor
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
15067009 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
19438409 GOA
Cellular Component GO Annotation Evidence References Source
part of ankyrin-1 complex IDA
IDA: Inferred from direct assay
35835865 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GYPA Protein Structure

Glycophorin_A

Glycophorin_A: Glycophorin A (28 - 147)

  • 0
  • 100
  • 150 a.a.
Protein Preferred Names Protein Names

glycophorin-A

  • MN sialoglycoprotein

GYPA Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
GYPA P02724 IL10RA Homo sapiens Q13651 32296183
Intra
GYPA P02724 IL10RA Homo sapiens Q13651 32296183
Intra
GYPA P02724 IL10RA Homo sapiens Q13651 32296183
Intra
GYPA P02724 TMBIM6 Homo sapiens P55061 32296183
Intra
GYPA P02724 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
GYPA P02724 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
GYPA P02724 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
GYPA P02724 GPX8 Homo sapiens Q8TED1 32296183
Intra
GYPA P02724 GPX8 Homo sapiens Q8TED1 32296183
Intra
GYPA P02724 TLCD4 Homo sapiens Q96MV1 32296183
Intra
GYPA P02724 TLCD4 Homo sapiens Q96MV1 32296183
Intra
GYPA P02724 TLCD4 Homo sapiens Q96MV1 32296183
Intra
GYPA P02724 GPRC5D Homo sapiens Q9NZD1 32296183
Intra
GYPA P02724 GPRC5D Homo sapiens Q9NZD1 32296183
Intra
GYPA P02724 GPRC5D Homo sapiens Q9NZD1 32296183
Intra
GYPA P02724 TMEM154 Homo sapiens Q6P9G4 32296183
Intra
GYPA P02724 TMEM154 Homo sapiens Q6P9G4 32296183
Intra
GYPA P02724 TMEM154 Homo sapiens Q6P9G4 32296183
Intra
GYPA P02724 GOLT1A Homo sapiens Q6ZVE7 32296183
Intra
GYPA P02724 GOLT1A Homo sapiens Q6ZVE7 32296183
Intra
GYPA P02724 GOLT1A Homo sapiens Q6ZVE7 32296183
Intra
GYPA P02724 ANKRD29 Homo sapiens Q8N6D5 32296183
Intra
GYPA P02724 ANKRD29 Homo sapiens Q8N6D5 32296183
Intra
GYPA P02724 ANKRD29 Homo sapiens Q8N6D5 32296183
Intra
GYPA P02724 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
GYPA P02724 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
GYPA P02724 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
GYPA P02724 FAM209A Homo sapiens Q5JX71 32296183
Intra
GYPA P02724 FAM209A Homo sapiens Q5JX71 32296183
Intra
GYPA P02724 FAM209A Homo sapiens Q5JX71 32296183
Intra
GYPA P02724 CLDN5 Homo sapiens O00501 32296183
Intra
GYPA P02724 CLDN5 Homo sapiens O00501 32296183
Intra
GYPA P02724 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
GYPA P02724 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
GYPA P02724 ELOVL4 Homo sapiens Q9GZR5 32296183
Cross
GYPA P02724 EBP Plasmodium reichenowi Q9N9G9
SPR
24297912
Cross
GYPA P02724 EBP Plasmodium reichenowi Q9N9G9 24297912
Intra
GYPA P02724 EBA-175 Plasmodium sp. chimpanzee clade C3 V9XTM1
SPR
24297912
Intra
GYPA P02724 EBA-175 Plasmodium sp. chimpanzee clade C3 V9XTM1 24297912
Intra
GYPA P02724 FFAR2 Homo sapiens O15552 32296183
Intra
GYPA P02724 FFAR2 Homo sapiens O15552 32296183
Intra
GYPA P02724 LAPTM5 Homo sapiens Q13571 32296183
Intra
GYPA P02724 LAPTM5 Homo sapiens Q13571 32296183
Intra
GYPA P02724 LAPTM5 Homo sapiens Q13571 32296183
Intra
GYPA P02724 SGTA Homo sapiens O43765 32296183
Intra
GYPA P02724 SGTA Homo sapiens O43765 32296183
Intra
GYPA P02724 EBP Homo sapiens Q15125 32296183
Intra
GYPA P02724 EBP Homo sapiens Q15125 32296183
Intra
GYPA P02724 EBP Homo sapiens Q15125 32296183
Intra
GYPA P02724 SAR1A Homo sapiens Q9NR31 32296183
Intra
GYPA P02724 SAR1A Homo sapiens Q9NR31 32296183
Intra
GYPA P02724 SAR1A Homo sapiens Q9NR31 32296183
Intra
GYPA P02724 SLC4A1 Homo sapiens P02730 19438409
Intra
GYPA P02724 ccsb orf id: 2260 Homo sapiens EBI-22326698 32296183
Intra
GYPA P02724 SLC4A1 Homo sapiens P02730 19438409
Intra
GYPA P02724 SLC4A1 Homo sapiens P02730 19438409
Intra
GYPA P02724 KEAP1 Homo sapiens Q14145 32296183
Intra
GYPA P02724 GYPA Homo sapiens P02724 23155421
Intra
GYPA P02724 KEAP1 Homo sapiens Q14145 32296183
Intra
GYPA P02724 GYPA Homo sapiens P02724 14681217
Intra
GYPA P02724 ccsb orf id: 2260 Homo sapiens EBI-22326698 32296183
Intra
GYPA P02724 GYPA Homo sapiens P02724 15067009
Intra
GYPA P02724 KEAP1 Homo sapiens Q14145 32296183
Intra
GYPA P02724 EVA1A Homo sapiens Q9H8M9 32296183
Intra
GYPA P02724 EVA1A Homo sapiens Q9H8M9 32296183
Intra
GYPA P02724 EVA1A Homo sapiens Q9H8M9 32296183
Intra
GYPA P02724 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
GYPA P02724 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
GYPA P02724 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
GYPA P02724 SGTB Homo sapiens Q96EQ0 32296183
Intra
GYPA P02724 SGTB Homo sapiens Q96EQ0 32296183
Intra
GYPA P02724 SGTB Homo sapiens Q96EQ0 32296183
Intra
GYPA P02724 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
GYPA P02724 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
GYPA P02724 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
GYPA P02724 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
GYPA P02724 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
GYPA P02724 TMEM14B Homo sapiens Q9NUH8 32296183
Cross
GYPA P02724 q8ibe8_plaf7 Plasmodium falciparum Q8IBE8 24297912
Cross
GYPA P02724 q8ibe8_plaf7 Plasmodium falciparum Q8IBE8
SPR
24297912
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant GYPA Proteins

Cat. No. Product Name Accession Purity
HY-P71741 GYPA/CD235a Protein, Human (P.pastoris, His) A0A0C4DFT7 (L20-E91) ≥ 90%, as determined by reducing SDS-PAGE.
HY-P72218 GYPA/CD235a Protein, Human (GST) A0A0C4DFT7 (L20-E91) ≥ 90%, as determined by reducing SDS-PAGE.
HY-P72219 GYPA/CD235a Protein, Human (His) A0A0C4DFT7 (L20-E91) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P75151 GYPA/CD235a Protein, Human (E24G, HEK293, His) P02724-1 (S21-E91, E24G) ≥ 95%, as determined by reducing SDS-PAGE.

GYPA Antibodies

Cat. No. Product Name Application Reactivity
HY-P81406 Glycophorin A Antibody (YA1151) IHC-P Human
HY-P81406A Glycophorin A Antibody (YA1151)(PBS only) IHC-P Human
HY-P83666M Human CD235 Antibody (APC) (YA3400) FC Human
HY-P85916 Glycophorin A Antibody (YA5608) IHC-P, WB, ICC/IF, ELISA Human
HY-P87180 CD235a Antibody (YA6871) FC, ELISA Human
HY-P87180A CD235a Antibody (YA6871)(PBS only) FC, ELISA Human

Related Diseases

Diseases Alias
Malaria
  • Malaria, Susceptibility To

  • Malaria, Resistance To

  • Malaria, Cerebral

  • Cerebral Malaria

  • Malaria, Severe, Susceptibility To

  • Malaria, Severe, Resistance To

  • Malaria, Cerebral, Susceptibility To

  • Induced Malaria

  • Malaria, Vivax, Protection Against

  • Malaria, Severe

  • Malaria, Cerebral, Reduced Risk Of

  • Malaria, Protection Against

  • Resistance To Malaria Due To G6pd Deficiency

  • Malaria Due To G6pd Deficiency

  • Malarial Encephalitis

  • CM

  • Malaria Cerebral

  • Susceptibility To Malaria

  • Acute Pernicious Fever

  • Aestivo-Autumnal Fever

  • Aestivo Autumnal Malaria

  • Chagres Fever

  • Continued Malaria Fever

  • Estivo-Autumnal Fever

  • Estivo-Autumnal Malaria

  • Estivo-Autumnal Malarial Fever

  • Falciparum Fever

  • Malignant Tertian Fever

  • Malignant Tertian Malaria

  • Pernicious Intermittent Fever

  • Pernicious Malaria

  • Quotidian Malaria

  • Subtertian Fever

  • Subtertian Malaria Fever

  • Subtertian Malignant Tertian Malaria

  • Tropical Malaria

  • Algid Malaria

  • Bilious Haemoglobinuric Fever

  • Black Water Fever

  • Blackwater Fever

  • Malarial Blackwater Fever

  • Severe Malarial Falciparum

  • West African Fever

  • Malarial Haematinuria

  • Haemoglobinuric Fever

  • Haemoglobinuric Malaria

  • Severe Plasmodium Falciparum Malaria

  • Malarial Haemoglobinuria

  • Malarial Haematuria

  • Falciparum Malaria [Malignant Tertian]

  • Malaria Tropica

  • Malarial Shock

  • Chagres Virus Disease

  • Malignant Malaria

  • Mtm - [Malignant Tertian Malaria]

  • Tm -[Malignant Tertian Malaria]

  • Panama Fever

  • St - [Subtertian Malaria]

  • Malarial Quotidian

  • Benign Tertian Malaria

  • Tertian Ague

  • Vivax Fever

  • Plasmodium Vivax Malaria Nos

  • Btm - [Benign Tertian Malaria]

  • Bt - [Benign Tertian Malaria]

  • Vivax Malaria

  • Benign Tertian Vivax Malaria

  • Tertian Malaria

  • Quartan Malaria

  • Quartan Ague

  • Quartan Fever

  • Plasmodium Malariae Malaria Nos

  • Quartan Malarial

  • Malaria By Plasmodium Malariae

  • Malariae Malaria

  • Ovale Tertian Malaria

  • Plasmodium Ovale Fever

  • Malaria Fever By Plasmodium Ovale

  • Ovale Malaria

  • Malaria By Plasmodium Ovale

  • Malarial Ovale

  • Marsh Fever

  • Remittent Congestive Fever

  • Coastal Fever

  • Remittent Gastric Fever

  • Miasmatic Fever

  • Congestive Remittent Fever

  • Intermittent Fever

  • Jungle Fever

  • Paludism

  • Cameroon Fever

  • Ague

  • Corsican Fever

  • Intermittent Bilious Fever

  • Disease Due To Plasmodiidae

  • Malarial Fever

  • Plasmodiosis

  • Remittent Fever

  • Roman Fever

  • Malaria Fever Nos

  • Malaria Nos

  • Paludal Fever

  • Clinically Diagnosed Malaria

  • Clinically Diagnosed Malaria Without Parasitological Confirmation

  • Congestive Fever

  • Malarial Cachexia

  • Marsh Cachexia

  • Paludal Cachexia

  • Recurrent Malaria

  • Remittent Malaria

Hepatitis A
  • Viral Hepatitis A

  • Viral Hepatitis, Type A

Pyridoxine-Responsive Sideroblastic Anemia
Hereditary Spherocytosis
  • Congenital Spherocytic Hemolytic Anemia

  • Spherocytic Anemia

  • Congenital Spherocytosis

  • Spherocytosis, Type 1

  • Minkowski Chauffard Syndrome

  • Hs

  • Minkowski-Chauffard Disease

  • Minkowski-Chauffard Syndrome

  • Spherocytosis Hereditary

  • Spherocytosis, Hereditary

  • Anemia, Hereditary Spherocytic Hemolytic

Anemia, Autoimmune Hemolytic
  • Autoimmune Hemolytic Anemia

  • Idiopathic Autoimmune Hemolytic Anemia

  • Immuno-Hemolytic Anemia

  • Anemia, Hemolytic, Autoimmune

  • Autoimmune Haemolytic Anaemia

  • Autoimmune Hemolytic Anaemia

  • Acquired Autoimmune Hemolytic Anemia

  • Anemia Hemolytic Autoimmune

  • Familial Auto-Immune Hemolytic Anemia

  • Aha

  • Aiha

Gastric Teratoma
  • Teratoma Of Stomach

Acute Erythroid Leukemia
  • Acute Erythroleukemia

  • Di Guglielmo'S Syndrome

  • Aml M6

  • Acute Myeloid Leukemia Fab-M6

  • Acute Myeloid Leukemia M6

  • Erythroleukemia

  • Aml-M6

  • Acute Erythroleukemia M6a Subtype

  • Acute Erythroleukemia M6b Subtype

  • Di Guglielmo Syndrome

  • Acute Myeloid Leukemia, M6 Type

  • Acute Erythroblastic Leukemia

  • Acute Erythroleukemia - M6a Subtype

  • Acute Erythroleukemia - M6b Subtype

  • Acute Erythraemia And Erythroleukaemia

  • Acute Erythroid Leukaemia Without Mention Of Remission

  • Erythraemia

  • Erythraemic Myelosis

  • Erythroleukaemia

  • Acute Erythraemic Myelosis

  • Acute Erythraemia

Malignant Gastric Germ Cell Tumor
  • Germ Cell Tumor Of The Stomach

  • Germ Cell Tumour Of The Stomach

  • Malignant Gastric Germ Cell Tumour

Diamond-Blackfan Anemia
  • Congenital Pure Red Cell Aplasia

  • Aase Syndrome

  • Erythrogenesis Imperfecta

  • Anemia, Diamond-Blackfan

  • Congenital Hypoplastic Anemia

  • Aase-Smith Ii Syndrome

  • Bds

  • Blackfan-Diamond Anemia

  • Congenital Prca

  • Congenital Hypoplastic Anemia, Blackfan-Diamond Type

  • Dba

  • Blackfan - Diamond Syndrome

  • Chronic Constitutional Pure Red Cell Anaemia

  • Anemia Diamond Blackfan Type

  • Anemia Congenital Erythroid Hypoplastic

  • Aregenerative Anemia Chronic Congenital

  • Blackfan Diamond Syndrome

  • Red Cell Aplasia, Pure Hereditary

  • Aase-Smith Syndrome Ii

  • Bda

  • Blackfan Diamond Anemia

  • Blackfan-Diamond Disease

  • Blackfan-Diamond Syndrome

  • Chronic Congenital Agenerative Anemia

  • Congenital Erythroid Hypoplastic Anemia

  • Congenital Hypoplastic Anemia Of Blackfan And Diamond

  • Congenital Pure Red Cell Anemia

  • Hypoplastic Congenital Anemia

  • Inherited Erythroblastopenia

  • Pure Hereditary Red Cell Aplasia

  • Anemia, Hypoplastic, Congenital

  • Anemia Hypoplastic Congenital

  • Fanconi Anemia

  • Constitutional Aplastic Anemia

  • Diamond-Blackfan Anemia 1

  • Aase Smith Syndrome 2

  • Congenital Red Cell Aplasia

  • Red Cell Aplasia Of Infants

  • Pure Red Cell Aplasia Of Infants

  • Congenital Red Cell Aplastic Anaemia

  • Congenital Pure Red Cell Anaemia

  • Congenital Erythroid Hypoplasia

  • Pearson Marrow-Pancreas Syndrome

Anemia, Congenital Dyserythropoietic, Type Ia
  • Congenital Dyserythropoietic Anemia Type I

  • Cda I

  • CDAN1A

  • Congenital Dyserythropoietic Anemia Type 1

  • Congenital Dyserythropoietic Anemia Type Ia

  • Congenital Dyserythropoietic Anemia, Type I

  • Anemia, Congenital Dyserythropoietic, Type I

  • Cda Type 1

  • Cda Type I

  • Cda Ia

  • Dyserythropoietic Anemia, Congenital Type 1

  • Anemia, Congenital Dyserythropoietic, Type 1a

  • Dyserythropoietic Anemia, Congenital, Type Ia

  • Cda, Type Ia

  • Congenital Dyserythropoietic Anaemia Type 1

  • Congenital Dyserythropoietic Anaemia Type I

  • Anemia, Dyserythropoietic, Congenital Type 1

  • Type I Congenital Dyserythropoietic Anemia

  • Anemia, Congenital Dyserythropoietic, 1a

  • Anemia, Dyserythropoietic, Congenital, Type Ia

Carrion'S Disease
  • Oroya Fever

  • Carrion Disease

  • Bartonellosis Due To Bartonella Bacilliformis Infection

  • Bartonella Infections

  • Systemic Bartonellosis Due To Bartonella Bacilliformis

  • Systemic Carrión Disease

  • Systemic Bartonellosis

  • Bartonella Fever

Hereditary Elliptocytosis
  • Congenital Elliptocytosis

  • Ovalocytosis

  • Elliptocytosis, Hereditary

  • He

  • Elliptocytosis Hereditary

  • Congenital Ovalocytosis

  • Elliptocytosis

  • Hereditary Elliptocytosis With Infantile Poikilocytosis

  • Hereditary Ovalocytosis

  • Oval Erythrocytosis

  • He - [Hereditary Elliptocytosis]

  • Elliptocytosis Anaemia

Duodenum Adenoma
Myelodysplastic Syndrome
  • Myelodysplastic Syndromes

  • Myelodysplasia

  • MDS

  • Myelodysplastic Syndrome Included

  • Myelodysplastic Syndrome, Susceptibility To, Included

  • Myelodysplastic Syndrome, Somatic

  • Myelodysplastic Syndrome, Susceptibility To

Fetal Erythroblastosis
  • Erythroblastosis, Fetal

  • Ef - Erythroblastosis Foetalis

  • Erythroblastosis Fetalis

  • Haemolytic Disease Due To Rhesus Isoimmunisation

  • Rhesus Isoimmunisation Of The Newborn

Myasthenic Syndrome, Congenital, 3a, Slow-Channel
  • Congenital Myasthenic Syndrome 3a

  • CMS3A

  • Congenital Myasthenic Syndrome 3a, Slow-Channel

  • Myasthenic Syndrome, Congenital, Type 3a, Slow-Channel

Congenital Hemolytic Anemia
  • Anemia Hemolytic Congenital

  • Anemia, Hemolytic, Congenital

  • Congenital Hemolytic Anaemia

  • Hereditary Hemolytic Anaemia

  • Hereditary Hemolytic Anemia

Anemia Of Prematurity
Myeloproliferative Syndrome, Transient
  • Transient Abnormal Myelopoiesis

  • Transient Myeloproliferative Syndrome

  • Transient Myeloproliferative Disease

  • Mst

  • Tam

  • Leukemia, Transient, Of Down Syndrome

  • Tmd

  • Leukemia, Transient

  • Transient Leukemia

  • Transient Leukemia Of Down Syndrome

Sickle Cell Anemia
  • Hemoglobin Sc Disease

  • Anemia, Sickle Cell

  • Hbsc Disease

  • Sickle Cell-Hemoglobin C Disease Syndrome

  • Hb Ss Disease

  • Sickle Cell Trait

  • Drepanocytosis

  • Haemoglobin Sc Disease

  • Hb Sc Disease

  • Hb-S/Hb-C Disease

  • Hb-Ss Disease Without Crisis

  • Hemoglobin S Disease Without Crisis

  • Sickle Cell Anaemia

  • Sickle-Cell/Hb-C Disease Without Crisis

  • Sickle Cell - Hemoglobin C Disease

  • Hbs Disease

  • Hemoglobin S Disease

  • Sickling Disorder Due To Hemoglobin S

  • SKCA

  • Sickle Cell Disease

  • Sickle Cell-Hemoglobin C Disease

  • Sickle-Cell Disease Carrier

  • Sickle-Cell Heterozygous Disorder

  • Haemoglobin A-S Genotype

  • Hb-S - [Sickle Cell Haemoglobin] Carrier

  • Sickle Cell Haemoglobin Trait

  • As - [Sickle Cell Trait]

  • Hbas - [Sickle Cell Haemoglobin Trait]

  • Sickle-Cell Trait Haemoglobin Disease

  • Haemoglobin Sickle Cell Trait Disorder

  • Heterozygous Sickle Cell Trait

  • Hbas - [Heterozygous Haemoglobin S]

Hemoglobinopathy
  • Hemoglobinopathies

Plasmodium Vivax Malaria
  • Malaria, Vivax

  • Malaria By Plasmodium Vivax

  • Vivax Malaria

  • Malaria Vivax

Beta-Thalassemia Major
  • Cooley'S Anemia

  • Cooley Anemia

  • Mediterranean Anemia

Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema
  • Dehydrated Hereditary Stomatocytosis

  • Hereditary Xerocytosis

  • Xerocytosis, Hereditary

  • Pshk1

  • Pseudohyperkalemia Edinburgh

  • Dehydrated Hereditary Stomatocytosis With Or Without Pseudohyperkalemia And/Or Perinatal Edema

  • DHS1

  • Dhs

  • Hereditary Desiccytosis

  • Dehydrated Hereditary Stomatocytosis 1

  • Desiccytosis, Hereditary

  • Pseudohyperkalemia, Familial, 1, Due To Red Cell Leak

  • Pseudohyperkalemia Familial 1, Due To Red Cell Leak

  • Desiccytosis Hereditary

  • Xerocytosis Hereditary

  • Familial Pseudohyperkalemia 1 Due To Red Cell Leak

  • Stomatocytosis, Dehydrated, Hereditary, With/Without Pseudohyperkalemia And/Or Perinatal Edema

  • Xerocytosis

Parasitic Protozoa Infectious Disease
  • Protozoan Infections

  • Mastigophora Infectious Disease

  • Sarcomastigophora Infectious Disease

Hemoglobin D Disease
  • Hb-D Disease

  • Punjab Disease

  • Los Angeles Disease

  • Hb D Los Angeles Disease

  • Hb D Punjab Disease

Glucosephosphate Dehydrogenase Deficiency
  • G6pd Deficiency

  • Glucose-6-Phosphate Dehydrogenase Deficiency

  • Deficiency Of Glucose-6-Phosphate Dehydrogenase

  • Glucose 6 Phosphate Dehydrogenase Deficiency

  • Deficiency Of G-6pd

  • G6pdd

Hemolytic Anemia
  • Anemia, Hemolytic

  • Anemia Hemolytic

  • Anaemia Due To Other Disorders Of Glutathione Metabolism

  • Chronic Non Spherocytic Anaemia

  • G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia

  • Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency

  • Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia

  • Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia

  • Favism Anaemia

  • Haemolytic Anaemia Due Tog6pd Deficiency

  • Favism

  • Pentose Phosphate Pathway Disorder Anaemia

  • Anaemia Due To Pentose Phosphate Pathway Defect

Deficiency Anemia
  • Anemia

  • Deficiency Anemias

  • Anaemia

Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus GYPA RGD RGD:1582935
Mus musculus GYPA MGD MGI:95880
Others GYPA NCBI