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CD69 CD69 molecule [ Homo sapiens (human) ]

Gene ID: 969, updated on 12-May-2016
Official Symbol
CD69provided by HGNC
Official Full Name
CD69 moleculeprovided by HGNC
Primary source
HGNC:HGNC:1694
See related
Ensembl:ENSG00000110848 HPRD:00119; MIM:107273; Vega:OTTHUMG00000168481
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
AIM; EA1; MLR-3; CLEC2C; GP32/28; BL-AC/P26
Summary
This gene encodes a member of the calcium dependent lectin superfamily of type II transmembrane receptors. Expression of the encoded protein is induced upon activation of T lymphocytes, and may play a role in proliferation. Furthermore, the protein may act to transmit signals in natural killer cells and platelets. [provided by RefSeq, Aug 2011]
Orthologs
Location:
12p13
Exon count:
5
Annotation release Status Assembly Chr Location
107 current GRCh38.p2 (GCF_000001405.28) 12 NC_000012.12 (9752486..9760901, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (9905082..9913497, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369652 Neighboring gene C-type lectin like 1 Neighboring gene uncharacterized LOC105369653 Neighboring gene acidic repeat containing pseudogene Neighboring gene killer cell lectin like receptor F1

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

NHGRI GWAS Catalog

Description
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.
NHGRI GWA Catalog

Protein interactions

Protein Gene Interaction Pubs
Envelope surface glycoprotein gp120 env HIV-1 gp120 significantly inhibits CD69 expression in phytohemagglutinin-stimulated T cells in vitro and may also affect T-cell activation in vivo PubMed
Nef nef Cells expressing HIV-1 Nef from long-term non-progressors and progressive infection patients induce higher surface levels of CD69 and CD25 than cells producing HIV-2 or SIV Nef PubMed
nef HIV-1 Nef protein with an intact SH3-binding domain expressed in the productively infected monocyte-derived macrophages is required for the enhanced expression of CD69 on the cell surface PubMed
nef Functional Nef is required for the activation of resting CD4+ T cells by upregulating CD69 expression on cell surface PubMed
nef HIV-1 Nef downregulates CD69 in Jurkat cells in a concentration-dependent manner PubMed
nef HIV-1 Nef blocks a receptor-proximal event in CD3 signaling by downregulating CD69 expression on the cell surface; mutations at amino acid residues P72, P75, R105 and R106 in Nef disrupts the ability of Nef to block CD3 signaling PubMed
Tat tat HIV-1 Tat binds to a cell surface receptor and activates a cell surface-mediated signal pathway in K562 cells, leading to the activation of NF-kappa B and the induction of CD69 PubMed
Vpr vpr Human endothelial cell (EC)-stimulated virus-producing cells (p24(high) T cells) are activated to sometimes express CD69 (but not CD25, HLA-DR, VLA-1, or effector cytokines) in the presence of HIV-1 Vpr PubMed

Go to the HIV-1, Human Interaction Database

Products Interactant Other Gene Complex Source Pubs Description

Markers

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
calcium ion binding IEA
Inferred from Electronic Annotation
more info
 
carbohydrate binding IEA
Inferred from Electronic Annotation
more info
 
protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
transmembrane signaling receptor activity TAS
Traceable Author Statement
more info
PubMed 
Process Evidence Code Pubs
cellular response to drug IEA
Inferred from Electronic Annotation
more info
 
signal transduction IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
external side of plasma membrane IEA
Inferred from Electronic Annotation
more info
 
integral component of plasma membrane TAS
Traceable Author Statement
more info
PubMed 
Preferred Names
early activation antigen CD69
Names
C-type lectin domain family 2, member C
CD69 antigen (p60, early T-cell activation antigen)
activation inducer molecule (AIM/CD69)
early T-cell activation antigen p60
early lymphocyte activation antigen
leukocyte surface antigen Leu-23

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001781.2NP_001772.1  early activation antigen CD69

    See identical proteins and their annotated locations for NP_001772.1

    Status: REVIEWED

    Source sequence(s)
    AC007068, Z22576
    Consensus CDS
    CCDS8604.1
    UniProtKB/Swiss-Prot
    Q07108
    UniProtKB/TrEMBL
    Q53ZX0
    Related
    ENSP00000228434, OTTHUMP00000238849, ENST00000228434, OTTHUMT00000399876
    Conserved Domains (1) summary
    cd03593
    Location:85196
    CLECT_NK_receptors_like; C-type lectin-like domain (CTLD) of the type found in natural killer cell receptors (NKRs)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 107 details...

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p2 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p2 Primary Assembly

    Range
    9752486..9760901 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate CHM1_1.1

Genomic

  1. NC_018923.2 Alternate CHM1_1.1

    Range
    9874021..9882437 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_026671.1: Suppressed sequence

    Description
    NR_026671.1: This RefSeq was temporarily suppressed because currently there is not sufficient data to support this transcript.
  2. NR_026672.1: Suppressed sequence

    Description
    NR_026672.1: This RefSeq was temporarily suppressed because currently there is not sufficient data to support this transcript.