SLAMF1 - signaling lymphocytic activation molecule family member 1 Gene

Also Known as SLAM; CD150; CDw150

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6504

About SLAMF1

Cytogenetic location: 1q23.3 Genomic coordinates (GRCh38): 1:160,608,106-160,647,044 (from NCBI)

This gene has 3 transcripts (splice variants), 99 orthologues and 9 paralogues. Biased expression in lymph node (RPKM 8.7), appendix (RPKM 6.0) and 11 other tissues.

Summary

Enables SH2 domain binding activity and identical protein binding activity. Involved in several processes, including negative regulation of CD40 signaling pathway; negative regulation of cytokine production; and positive regulation of MAPK cascade. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

SLAMF1 Products (2)

mRNA Protein Name
NM_001330754.2 NP_001317683.1 signaling lymphocytic activation molecule isoform a precursor
NM_003037.5 NP_003028.1 signaling lymphocytic activation molecule isoform b precursor
Molecular Function GO Annotation Evidence References Source
enables SH2 domain binding IDA
IDA: Inferred from direct assay
9774102 GOA
enables cell adhesion mediator activity IDA
IDA: Inferred from direct assay
10972291 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
21217702 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9774102 GOA
enables virus receptor activity IDA
IDA: Inferred from direct assay
10972291 GOA
Biological Process GO Annotation Evidence References Source
involved in myeloid dendritic cell activation involved in immune response IDA
IDA: Inferred from direct assay
16317102 GOA
involved in negative regulation of CD40 signaling pathway IDA
IDA: Inferred from direct assay
16317102 GOA
involved in negative regulation of interleukin-12 production IDA
IDA: Inferred from direct assay
16317102 GOA
involved in negative regulation of interleukin-6 production IDA
IDA: Inferred from direct assay
16317102 GOA
involved in negative regulation of tumor necrosis factor production IDA
IDA: Inferred from direct assay
16317102 GOA
involved in positive regulation of ERK1 and ERK2 cascade IDA
IDA: Inferred from direct assay
20231852 GOA
involved in positive regulation of JNK cascade IDA
IDA: Inferred from direct assay
20231852 GOA
Cellular Component GO Annotation Evidence References Source
is active in plasma membrane IDA
IDA: Inferred from direct assay
10972291 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

SLAMF1 Protein Structure

SLAM

SLAM: Signaling lymphocytic activation molecule (SLAM) protein (1 - 126)

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

signaling lymphocytic activation molecule

  • IPO-3

SLAMF1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SLAMF1 Q13291 SH2D1A Homo sapiens O60880-1 15841490
Intra
SLAMF1 Q13291 SH2D1A Homo sapiens O60880
Y2H
9774102
Intra
SLAMF1 Q13291 SLAMF1 Homo sapiens Q13291
SPR
21217702
Intra
SLAMF1 Q13291 SH2D1A Homo sapiens O60880
FPS
11477068
Intra
SLAMF1 Q13291 SH2D1A Homo sapiens O60880
NMR
11823424
Intra
SLAMF1 Q13291 MAP4K1 Homo sapiens Q92918 20231852
Intra
SLAMF1 Q13291 SH2D1A Homo sapiens O60880 12545174
Intra
SLAMF1 Q13291 SLAMF1 Homo sapiens Q13291 21982860
Intra
SLAMF1 Q13291 SH2D1A Homo sapiens O60880 20231852
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SLAMF1 Proteins

Cat. No. Product Name Accession Purity
HY-P7788 CD150/SLAMF1 Protein, Human (HEK293, His) Q13291-1 (A21-P237) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P72413 CD150/SLAMF1 Protein, Human (Biotinylated, HEK293, His-Avi) Q13291-1 (A21-P237) ≥ 95%, as determined by reducing SDS-PAGE.

SLAMF1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82894 SLAMF1 Antibody (YA2639) WB, IP, FC Human

Related Diseases

Diseases Alias
Measles
  • Rubeola

  • Morbilli

  • Measles Nos

  • Koplik Spots

Subacute Sclerosing Panencephalitis
  • SSPE

  • Dawson Encephalitis

  • Immunosuppressive Measles Encephalitis

  • Subacute Sclerosing Leukoencephalitis

  • Panencephalitis, Subacute Sclerosing

  • Subacute Sclerosing Leukoencephalopathy

  • Van Bogaert'S Sclerosing Leukoencephalitis

  • Dawson Disease

  • Subacute Inclusion Body Encephalitis

  • Van Bogaert Disease

  • Van Bogaert Encephalitis

  • Measles Inclusion Body Encephalitis

  • Mibe - [Measles Inclusion Body Encephalitis]

  • Sspe - [Subacute Sclerosing Panencephalitis]

  • Van Bogaert Leukoencephalitis

  • Van Bogaert Sclerosing Leukoencephalitis

  • Dawson Inclusion Body Encephalitis

  • Van Bogaert Sclerosing Leukoencephalopathy

  • Bodechtel Guttman Disease

  • Diffuse Sclerosing Encephalitis

Lymphoproliferative Syndrome
  • Lymphoproliferative Disorder

  • Lymphoproliferative Disorders

  • Lymphoproliferative Disorders, Susceptibility To

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

Selective Immunoglobulin Deficiency Disease
Dysgammaglobulinemia
Lymphoproliferative Syndrome, X-Linked, 2
  • XLP2

  • Xiap Deficiency

  • X-Linked Lymphoproliferative Syndrome 2

  • X-Linked Lymphoproliferative Disease Due To Xiap Deficiency

  • Xiap-Related Lymphoproliferative Disease, X-Linked

  • X-Linked Lymphoproliferative Syndrome Type 2

  • Xiap Deficiency Syndrome

Immune Deficiency Disease
  • Immunodeficiency

  • Primary Immunodeficiency

  • Primary Immunodeficiency Disease

  • Immunologic Deficiency Syndromes

  • Hypoimmunity

  • Immune Deficiency Disorder

  • Immunodeficiency Syndrome

  • Immune Disorder

  • Primary Immune Deficiency Disorder

  • Immune System Diseases

  • Human Immunodeficiency Virus Infection

  • Hiv - [Human Immunodeficiency Virus Infection]

  • Hiv Positive Nos

  • Hiv Disease

  • Acquired Immune Deficiency Syndrome-Related Complex

  • Aids-Like Syndrome

  • Aids-Related Complex Nos

  • Arc - [Aids-Related Complex]

  • Immunodeficiency Due To Human Immunodeficiency Virus Infection

  • Unspecified Human Immunodeficiency Virus Disease

  • Hiv Disease Nos

  • Human Immunodeficiency Virus Positive Nos

  • Hiv Nos

  • Deficiency Of Complement Initial Pathway

  • Deficiency Of Complement Terminal Pathway

  • Cfdd - [Complement Factor D Deficiency]

  • Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency

  • Nonfamilial Hypogammaglobulinaemia

  • Common Variable Immune Deficiency

  • Nonfamilial Agammaglobulinaemia

  • Common Variable Agammaglobulinaemia

  • Agammaglobulinaemia Nos

  • Agammaglobulinaemia Antibody Deficiency Syndrome

  • Hypogammaglobulinaemia Antibody Deficiency Syndrome

  • Acquired Agammaglobulinaemia Nos

  • Hypogammaglobulinaemia Nos

  • Hyper Igm

Trochlear Nerve Disease
  • Trochlear Nerve Diseases

  • Disorder Of Trochlear Nerve

  • Superior Oblique Muscle Innervation Disorder

  • Trochlear Nerve Disorder

  • Fourth Cranial Nerve Paresis

Lymphoproliferative Syndrome 2
  • Cd27 Deficiency

  • LPFS2

  • Combined Immunodeficiency Due To Cd27 Deficiency

  • Autosomal Recessive Lymphoproliferative Disease Due To Cd27 Deficiency

Viral Infectious Disease
  • Viral Disease

  • Arbovirus Infections

  • Virus Infection

  • Virus Diseases

  • Viral Infection

  • Viral Infections

  • Virus Infections

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]

Herpangina
  • Vesicular Pharyngitis

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

Lymphoma, Hodgkin, Classic
  • Hodgkin Lymphoma

  • Hodgkin Disease

  • Hodgkin'S Lymphoma

  • Hodgkins Lymphoma

  • Classic Hodgkin Lymphoma

  • CHL

  • Hodgkin Lymphoma, Susceptibility To

  • Hl

  • Hodgkin'S Sarcoma

  • Stage I Subdiaphragmatic Hodgkin Lymphoma

  • Stage Ii Subdiaphragmatic Hodgkin Lymphoma

  • Lymphoma, Hodgkin'S

  • Classic Hodgkin Disease

  • Hodgkin'S Disease

  • Lymphoma, Hodgkin, Susceptibility To

  • Hodgkin'S Disease Of Intrapelvic Lymph Nodes

  • Hodgkin'S Disease Of Lymph Nodes Of Inguinal Region And/Or Lower Limb

  • Malignant Lymphogranuloma

  • Malignant Lymphogranulomatosis

  • Malignant Hodgkin Lymphoma

  • Classical Hodgkin Lymphoma, Type Not Specified

Hemophagocytic Lymphohistiocytosis
  • Lymphohistiocytosis, Hemophagocytic

  • Haemophagocytic Syndrome

  • Lymphohistiocytosis Hemophagocytic

  • Hemophagocytic Syndrome

  • Familial Hemophagocytic Lymphocytosis

  • Histiocytoses Of Mononuclear Phagocytes

  • Haemophagocytic Lymphohistiocytosis Nos

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
Bos taurus SLAMF1 VGNC VGNC:34653
Canis familiaris SLAMF1 VGNC VGNC:46206
Mus musculus SLAMF1 MGD MGI:1351314
Macaca mulatta SLAMF1 VGNC VGNC:77378
Rattus norvegicus SLAMF1 RGD RGD:1560634
Felis catus SLAMF1 VGNC VGNC:65177
Others SLAMF1 NCBI