CD177 - CD177 molecule Gene

Also Known as NB1; PRV1; HNA2A; PRV-1; HNA-2a; NB1 GP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 57126

About CD177

Cytogenetic location: 19q13.31 Genomic coordinates (GRCh38): 19:43,353,686-43,366,081 (from NCBI)

This gene has 3 transcripts (splice variants), 97 orthologues and 2 paralogues. Biased expression in bone marrow (RPKM 83.5), colon (RPKM 72.9) and 1 other tissue.

Summary

This gene encodes a glycosyl-phosphatidylinositol (GPI)-linked cell surface glycoprotein that plays a role in neutrophil activation. The protein can bind platelet endothelial cell adhesion molecule-1 and function in neutrophil transmigration. Mutations in this gene are associated with myeloproliferative diseases. Over-expression of this gene has been found in patients with polycythemia rubra vera. Autoantibodies against the protein may result in pulmonary transfusion reactions, and it may be involved in Wegener's granulomatosis. A related pseudogene, which is adjacent to this gene on chromosome 19, has been identified. [provided by RefSeq, Apr 2014]

CD177 Products (1)

mRNA Protein Name
NM_020406.4 NP_065139.2 CD177 antigen precursor
Molecular Function GO Annotation Evidence References Source
enables calcium-dependent protein binding IPI
IPI: Inferred from physical interaction
17580308 GOA
enables integrin binding IPI
IPI: Inferred from physical interaction
21193407 GOA
enables protease binding IPI
IPI: Inferred from physical interaction
17244676 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence References Source
involved in cell adhesion IMP
IMP: Inferred from mutant phenotype
28807980 GOA
involved in cell-cell adhesion via plasma-membrane adhesion molecules IMP
IMP: Inferred from mutant phenotype
17580308 GOA
involved in cell-cell junction maintenance IMP
IMP: Inferred from mutant phenotype
23202369 GOA
involved in leukocyte cell-cell adhesion IMP
IMP: Inferred from mutant phenotype
17580308 GOA
involved in neutrophil extravasation IMP
IMP: Inferred from mutant phenotype
17580308 GOA
NOT involved in neutrophil migration IMP
IMP: Inferred from mutant phenotype
28240246 GOA
involved in neutrophil migration IMP
IMP: Inferred from mutant phenotype
28807980 GOA
involved in positive regulation of neutrophil degranulation IGI
IGI: Inferred from genetic interaction
21193407 GOA
involved in positive regulation of superoxide anion generation IGI
IGI: Inferred from genetic interaction
21193407 GOA
involved in protein localization to cell surface IMP
IMP: Inferred from mutant phenotype
17244676 GOA
involved in regulation of endocytosis IDA
IDA: Inferred from direct assay
28807980 GOA
involved in regulation of integrin-mediated signaling pathway IMP
IMP: Inferred from mutant phenotype
28807980 GOA
Cellular Component GO Annotation Evidence References Source
located in plasma membrane IDA
IDA: Inferred from direct assay
12675722 GOA
located in plasma membrane raft IDA
IDA: Inferred from direct assay
21193407 GOA
located in secretory granule membrane IDA
IDA: Inferred from direct assay
18462208 GOA
located in tertiary granule membrane IDA
IDA: Inferred from direct assay
18462208 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
Protein Preferred Names Protein Names

CD177 antigen

  • NB1 glycoprotein

CD177 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CD177 Q8N6Q3 KCNIP3 Homo sapiens Q9Y2W7 32296183
Intra
CD177 Q8N6Q3 KCNIP3 Homo sapiens Q9Y2W7 32296183
Intra
CD177 Q8N6Q3 KCNIP3 Homo sapiens Q9Y2W7 25416956
Intra
CD177 Q8N6Q3 KCNIP3 Homo sapiens Q9Y2W7 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CD177 Proteins

Cat. No. Product Name Accession Purity
HY-P7801 CD177 Protein, Human (HEK293, His) AAH29167.1 (L22-G407) ≥ 95%, as determined by reducing SDS-PAGE.

CD177 Antibodies

Cat. No. Product Name Application Reactivity
HY-P84674 CD177 Antibody (YA4371) WB, FC, ELISA Human
HY-P84674A CD177 Antibody (YA4371)(PBS only) WB, FC, ELISA Human

Related Diseases

Diseases Alias
Polycythemia
  • Erythrocythemia

  • Polycythemia Vera

  • Polycythaemia Due To High Altitude

Polycythemia Vera
  • PV

  • Polycythemia Rubra Vera

  • Prv

  • Osler-Vaquez Disease

  • Chronic Erythremia

  • Polycythaemia Rubra Vera

  • Primary Polycythemia

  • Vaquez Disease

  • Polycythemia Vera, Somatic

  • Osler-Vaquez Syndrome

  • Proliferative Polycythaemia

  • Polycythemia Ruba Vera

  • Acquired Primary Erythrocytosis

  • Heilmeyer-Schoner Disease

  • Vaquez Osler Disease

  • Primary Polycythaemia

Essential Thrombocythemia
  • Essential Thrombocytosis

  • Familial Thrombocytosis

  • Hemorrhagic Thrombocythemia

  • Hereditary Thrombocythemia

  • Primary Thrombocytosis

  • Idiopathic Thrombocythemia

  • Primary Thrombocythemia

  • Thrombocythemia, Essential

  • Essential Thrombocythaemia

  • Et

  • Familial Thrombocythemia

  • Thrombocythemia Essential

Myelofibrosis
  • Primary Myelofibrosis

  • Agnogenic Myeloid Metaplasia

  • Idiopathic Myelofibrosis

  • Myeloid Metaplasia

  • Myelofibrosis With Myeloid Metaplasia

  • Osteomyelofibrosis

  • Megakaryocytic Myelosclerosis

  • Myelosclerosis

  • Chronic Idiopathic Myelofibrosis

  • Myelofibrosis, Idiopathic

  • Myelofibrosis With Myeloid Metaplasia, Somatic

  • Myelofibrosis, Somatic

  • Aleukemic Myelosis

  • Bone Marrow Fibrosis

  • MYELOF

  • MMM

  • Agnogenic Myeloid Metaplasia With Myelofibrosis

  • Ammm

  • Myelosclerosis With Myeloid Metaplasia

  • Myelofibrosis Nos

Deep Leiomyoma
Myeloproliferative Neoplasm
  • Myeloproliferative Disorder

  • Chronic Myeloproliferative Disease

  • Myeloproliferative Neoplasms

  • Chronic Myeloproliferative Disorder

  • Cmpd

  • Cmpd, U

  • Chronic Myeloproliferative Disorders

  • Mpd

  • Mpn

  • Myeloproliferative Disorders

  • Myeloproliferative Disease

  • Campomelic Dysplasia

Neutropenia
  • Leukopenia

Thrombocytosis
  • Thrombocythaemia

Myopathy, Centronuclear, 1
  • Autosomal Dominant Centronuclear Myopathy

  • CNM1

  • Centronuclear Myopathy 1

  • Ad-Cnm

  • Myopathy, Centronuclear, Autosomal Dominant

  • Myotubular Myopathy, Autosomal Dominant

  • Centronuclear Myopathy, Autosomal, Modifier Of

  • Autosomal Dominant Myotubular Myopathy

  • Dnm2-Related Centronuclear Myopathy

  • Centronuclear Myopathy Autosomal Dominant

  • Myopathies, Structural, Congenital

  • Myopathy, Centronuclear, Type 1

Leukemia, Chronic Myeloid
  • Chronic Myeloid Leukemia

  • Chronic Myelogenous Leukemia

  • CML

  • Chronic Granulocytic Leukemia

  • Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib

  • Chronic Myeloid Leukaemia

  • Chronic Granulocytic Leukaemia

  • Chronic Myelogenous Leukaemia

  • Myeloid Leukemia, Chronic

  • Leukemia, Chronic Myelogenous

  • Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic

  • Cml - Chronic Myelogenous Leukemia

  • Cgl

  • Chronic Myelocytic Leukemia

  • Leukemia, Chronic Myeloid, Atypical

  • ACML

  • Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative

  • Myeloid Leukemia Chronic

  • Leukemia, Myeloid, Chronic

  • Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative

  • Cml- [Chronic Myeloid Leukaemia]

  • Cgl - [Chronic Granulocytic Leukaemia]

  • Chronic Myelocytic Leukaemia

Adult Hepatocellular Carcinoma
  • Adult Primary Hepatocellular Carcinoma

  • Adult Hepatoma

  • Adult Hcc

Myelodysplastic Syndrome
  • Myelodysplastic Syndromes

  • Myelodysplasia

  • MDS

  • Myelodysplastic Syndrome Included

  • Myelodysplastic Syndrome, Susceptibility To, Included

  • Myelodysplastic Syndrome, Somatic

  • Myelodysplastic Syndrome, Susceptibility To

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 CD177 RGD RGD:1562941
Macaca mulatta CD177 VGNC VGNC:70912
Mus musculus CD177 MGD MGI:1916141
Canis familiaris CD177 VGNC VGNC:38934
Bos taurus CD177 VGNC VGNC:27006
Others CD177 NCBI