SLAMF6 - SLAM family member 6 Gene

Also Known as KALI; NTBA; CD352; KALIb; Ly108; NTB-A; SF2000

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 114836

About SLAMF6

Cytogenetic location: 1q23.2-q23.3 Genomic coordinates (GRCh38): 1:160,485,036-160,523,255 (from NCBI)

This gene has 3 transcripts (splice variants), 132 orthologues and 9 paralogues. Biased expression in lymph node (RPKM 29.2), spleen (RPKM 15.5) and 7 other tissues.

Summary

The protein encoded by this gene is a type I transmembrane protein, belonging to the CD2 subfamily of the immunoglobulin superfamily. This encoded protein is expressed on Natural killer (NK), T, and B lymphocytes. It undergoes tyrosine phosphorylation and associates with the Src homology 2 domain-containing protein (SH2D1A) as well as with SH2 domain-containing phosphatases (SHPs). It functions as a coreceptor in the process of NK cell activation. It can also mediate inhibitory signals in NK cells from X-linked lymphoproliferative patients. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, May 2010]

SLAMF6 Products (4)

mRNA Protein Name
NM_001184714.2 NP_001171643.1 SLAM family member 6 isoform 1 precursor
NM_001184715.2 NP_001171644.1 SLAM family member 6 isoform 3 precursor
NM_001184716.2 NP_001171645.1 SLAM family member 6 isoform 4 precursor
NM_052931.5 NP_443163.1 SLAM family member 6 isoform 2 precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
11489943 GOA
Biological Process GO Annotation Evidence References Source
involved in T-helper 17 cell lineage commitment IDA
IDA: Inferred from direct assay
22184727 GOA
involved in positive regulation of interleukin-17 production IDA
IDA: Inferred from direct assay
22184727 GOA
involved in positive regulation of natural killer cell mediated cytotoxicity IDA
IDA: Inferred from direct assay
16920955 GOA
involved in positive regulation of type II interferon production IMP
IMP: Inferred from mutant phenotype
16920955 GOA
Cellular Component GO Annotation Evidence References Source
located in plasma membrane IDA
IDA: Inferred from direct assay
22184727 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

SLAMF6 Protein Structure

V-set

V-set: Immunoglobulin V-set domain (27 - 114)

Ig_3

Ig_3: Immunoglobulin domain (143 - 199)

  • 0
  • 100
  • 200
  • 300
  • 332 a.a.
Protein Preferred Names Protein Names

SLAM family member 6

  • NK-T-B-antigen

SLAMF6 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SLAMF6 Q96DU3 SH2D1B Homo sapiens O14796 16920955
Intra
SLAMF6 Q96DU3 SH2D1B Homo sapiens O14796 23346089
Intra
SLAMF6 Q96DU3 SH2D1A Homo sapiens O60880 22912825
Intra
SLAMF6 Q96DU3 SH2D1A Homo sapiens O60880 16920955
Intra
SLAMF6 Q96DU3 SH2D1A Homo sapiens O60880 23346089
Intra
SLAMF6 Q96DU3 SH2D1A Homo sapiens O60880 11489943
Intra
SLAMF6 Q96DU3 SH2D1A Homo sapiens O60880 24688028
Intra
SLAMF6 Q96DU3 RABAC1 Homo sapiens Q9UI14 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SLAMF6 Proteins

Cat. No. Product Name Accession Purity
HY-P71317 SLAMF6 Protein, Human (HEK293, His) Q96DU3-1 (L28-K225) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P72415 SLAMF6 Protein, Human (HEK293, His-Avi) Q96DU3-1 (Q22-K225) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P76645 SLAMF6 Protein, Human (HEK293) Q96DU3-1 (Q22-M226) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P76646 SLAMF6 Protein, Human (HEK293, Fc) Q96DU3-1 (Q22-M226) ≥ 95%, as determined by reducing SDS-PAGE.

SLAMF6 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81727 SLAMF6/CD352 Antibody (YA1472) FC, ELISA Human
HY-P82232 SLAMF6/CD352 Antibody (YA1977) WB, ICC/IF, IP Human
HY-P82232A SLAMF6/CD352 Antibody (YA1977)(PBS only) WB, ICC/IF, IP Human
HY-P84727 SLAMF6/CD352 Antibody (YA4424) IHC-P, FC, ELISA Human
HY-P84727A SLAMF6/CD352 Antibody (YA4424)(PBS only) IHC-P, FC, ELISA Human

Related Diseases

Diseases Alias
Selective Immunoglobulin Deficiency Disease
Lupus Erythematosus
  • Lupus

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus, Systemic

  • Subacute Cutaneous Lupus

  • Le - [Lupus Erythematosus]

Lymphoproliferative Syndrome
  • Lymphoproliferative Disorder

  • Lymphoproliferative Disorders

  • Lymphoproliferative Disorders, Susceptibility To

Dysgammaglobulinemia
Ovarian Cystic Teratoma
Lymphoproliferative Syndrome, X-Linked, 1
  • Lymphomatoid Papulosis

  • Duncan Disease

  • Purtilo Syndrome

  • X-Linked Lymphoproliferative Syndrome

  • Xlp

  • X-Linked Lymphoproliferative Disease

  • XLP1

  • Lyp

  • Lymphoproliferative Disease, X-Linked

  • Xlpd

  • X-Linked Lymphoproliferative Disease Due To Sh2d1a Deficiency

  • Ebv Infection, Severe, Susceptibility To

  • Ebvs

  • Immunodeficiency 5

  • Imd5

  • X-Linked Lymphoproliferative Syndrome 1

  • Epstein-Barr Virus Infection, Familial Fatal

  • Ebv Infection, Severe

  • Infectious Mononucleosis, Severe

  • Infectious Mononucleosis, Severe, Susceptibility To

  • Immunodeficiency, X-Linked Progressive Combined Variable

  • Epstein Barr Virus Infection, Familial Fatal

  • X-Linked Progressive Combined Variable Immunodeficiency 5

  • Epstein-Barr Virus-Induced Lymphoproliferative Disease In Males

  • Familial Fatal Epstein-Barr Infection

  • Severe Susceptibility To Ebv Infection

  • Severe Susceptibility To Infectious Mononucleosis

  • Sap Deficiency

  • Sh2d1a/Slam-Associated Protein Deficiency

  • X-Linked Lymphoproliferative Syndrome Type 1

  • X-Linked Progressive Combined Variable Immunodeficiency

  • Lymphoproliferative Syndrome, X-Linked

  • Sap

  • X-Linked Lymphoproliferative Disorder

Mature Teratoma Of The Ovary
Systemic Lupus Erythematosus
  • Lupus Nephritis

  • SLE

  • Disseminated Lupus Erythematosus

  • Systemic Lupus Erythematosus, Susceptibility To

  • Lupus Erythematosus, Systemic

  • Lupus Nephritis, Susceptibility To

  • Libman-Sacks Disease

  • Systemic Lupus Erythematosus Susceptibility To

  • Sle - Lupus Erythematosus, Systemic

  • Le Syndrome

  • Lupus

  • Lupus Erythematosus Systemic

  • Lupus Erythematosus, Systemic, Susceptibility To

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus

  • Systemic Lupus Erythematosus Nos

  • Sle - [Systemic Lupus Erythematosus]

Immunodeficiency, X-Linked, With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia
  • XMEN

  • X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection And Neoplasia

  • X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia

  • Immunodeficiency, X-Linked, With Magnesium Defect, Epstein-Barr Virus Infection And Neoplasia

  • Cid Due To Magt1 Deficiency

  • Combined Immunodeficiency Due To Magt1 Deficiency

  • X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection An

  • X-Linked Magnesium Deficiency With Epstein-Barr Virus Infection And Neoplasia

Lymphoproliferative Syndrome 2
  • Cd27 Deficiency

  • LPFS2

  • Combined Immunodeficiency Due To Cd27 Deficiency

  • Autosomal Recessive Lymphoproliferative Disease Due To Cd27 Deficiency

Pfeiffer Syndrome
  • Infectious Mononucleosis

  • Acs5

  • Craniofacial-Skeletal-Dermatologic Dysplasia

  • Acs V

  • Noack Syndrome

  • Gammaherpesviral Mononucleosis

  • Acrocephalosyndactyly Type 5

  • Pfeiffer Syndrome Type 3

  • Acrocephalosyndactyly, Type V

  • Glandular Fever

  • Pfeiffer Type Acrocephalosyndactyly

  • Pfeiffer Syndrome Type 2

  • Acrocephalosyndactylia Type V

  • Filatov'S Disease

  • Monocytic Angina

  • Mononucleosis

  • Pfeiffer'S Disease

  • Acsv

  • Acrocephalosyndactyly, Type 5

  • Craniofacial-Skeletal-Dermatologic Syndrome

  • Pfeiffer Syndrome Type 1

  • Classic Pfeiffer Syndrome

  • PS

  • Pfeiffer Syndrome Variant

  • Dysplasia, Craniofacial-Skeletal-Dermatologic

  • Pfeiffer

  • Kissing Disease

  • Infectious Adenitis

  • Pfeiffer Disease

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
Canis familiaris SLAMF6 VGNC VGNC:46207
Macaca mulatta SLAMF6 VGNC VGNC:77546
Bos taurus SLAMF6 VGNC VGNC:34654
Mus musculus SLAMF6 MGD MGI:1353620
Felis catus SLAMF6 VGNC VGNC:107939
Rattus norvegicus SLAMF6 RGD RGD:1561848
Others SLAMF6 NCBI