GYPB - glycophorin B (MNS blood group) Gene

Also Known as SS; GPB; GYP; MNS; GYPA; PAS-3; CD235b

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 2994

About GYPB

Cytogenetic location: 4q31.21 Genomic coordinates (GRCh38): 4:143,995,188-144,019,380 (from NCBI)

This gene has 17 transcripts (splice variants), 33 orthologues, 2 paralogues and is associated with 2 phenotypes. Restricted expression toward bone marrow (RPKM 2.7).

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. GYPB gene consists of 5 exons and has 97% sequence homology with GYPA from the 5' UTR to the coding sequence encoding the first 45 Amino acids. 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; also, 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. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]

GYPB Products (2)

mRNA Protein Name
NM_001304382.1 NP_001291311.1 glycophorin-B isoform 2
NM_002100.6 NP_002091.4 glycophorin-B isoform 1 precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 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

GYPB Protein Structure

Glycophorin_A

Glycophorin_A: Glycophorin A (21 - 90)

  • 0
  • 91 a.a.
Protein Preferred Names Protein Names

glycophorin-B

  • GYPB-A fusion

GYPB Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
GYPB P06028 UBQLN1 Homo sapiens Q9UMX0-2 25416956
Intra
GYPB P06028 S1PR3 Homo sapiens Q99500 32296183
Intra
GYPB P06028 S1PR3 Homo sapiens Q99500 32296183
Intra
GYPB P06028 S1PR3 Homo sapiens Q99500 32296183
Intra
GYPB P06028 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
GYPB P06028 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
GYPB P06028 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
GYPB P06028 UBQLN1 Homo sapiens Q9UMX0 25910212
Intra
GYPB P06028 UBQLN1 Homo sapiens Q9UMX0 25910212
Intra
GYPB P06028 UBQLN1 Homo sapiens Q9UMX0 25910212
Intra
GYPB P06028 UBQLN1 Homo sapiens Q9UMX0 25416956
Intra
GYPB P06028 REEP4 Homo sapiens Q9H6H4 32296183
Intra
GYPB P06028 REEP4 Homo sapiens Q9H6H4 32296183
Intra
GYPB P06028 REEP4 Homo sapiens Q9H6H4 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

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

Chronic Maxillary Sinusitis
  • Chronic Antritis

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

Hemolytic Disease Of Fetus And Newborn, Rh-Induced
  • Rh Deficiency Syndrome

  • Rh Disease

  • HDFNRH

  • Rh Fetomaternal Incompatibility

  • Rh-Null Syndrome

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

Congenital Dyserythropoietic Anemia
  • Congenital Dyshaematopoietic Anaemia

  • Dyserythropoietic Anemia, Congenital

  • Cda

  • Anemia, Dyserythropoietic, Congenital

  • Anemia Dyserythropoietic Congenital

  • Cda - [Congenital Dyserythropoietic Anaemia]

  • Dyserythropoietic Dyshaematopoietic Congenital Anaemia

  • Dyshaematopoietic Anaemia

  • Dyserythropoietic Anaemia

Urea Cycle Disorder
  • Urea Cycle Disorders

  • Urea Cycle Disorders, Inborn

  • Disorder Of Metabolism Of Ornithine, Citrulline, Argininosuccinic Acid, Arginine And Ammonia

  • Disorder Of Urea Cycle Metabolism

  • Urea Cycle Defect

  • Ucd

  • Disorder Of The Urea Cycle Metabolism

  • Disorder Of Urea Cycle

  • Disorders Of Metabolism Of Ornithine, Citrulline, Argininosuccinic Acid, Arginine And Ammonia

  • Ammonia Metabolic Disorder

Chronic Endophthalmitis
Panophthalmitis
Capillary Malformations, Congenital
  • Familial Multiple Nevi Flammei

  • Nevi Flammei, Familial Multiple

  • CMC

  • Port-Wine Stain

  • Capillary Malformations

  • Cmal

  • Familial Multiple Port-Wine Stains

  • Capillary Malformation

  • Capillary Malformations, Congenital, 1, Somatic, Mosaic

  • Congenital Capillary Malformations

  • Port-Wine Stain Familial Multiple

  • Hereditary Capillary Malformations

  • Capillary Malformations, Hereditary

  • Capillary Malformations, Congenital, Type 1, Somatic, Mosaic

  • Strawberry Nevus Of Skin

  • Naevus Flammeus

Purulent Endophthalmitis
  • Periocular Infection

  • Acute Endophthalmitis

  • Endophthalmia

  • Eye Infestation Nos

  • Intraocular Infection

  • Eye Infection Nos

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

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
Mus musculus GYPB MGD MGI:95880