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RELT RELT TNF receptor [ Homo sapiens (human) ]

Gene ID: 84957, updated on 2-Nov-2024

Summary

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Official Symbol
RELTprovided by HGNC
Official Full Name
RELT TNF receptorprovided by HGNC
Primary source
HGNC:HGNC:13764
See related
Ensembl:ENSG00000054967 MIM:611211; AllianceGenome:HGNC:13764
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
AI3C; TRLT; TNFRSF19L
Summary
The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is especially abundant in hematologic tissues. It has been shown to activate the NF-kappaB pathway and selectively bind TNF receptor-associated factor 1 (TRAF1). This receptor is capable of stimulating T-cell proliferation in the presence of CD3 signaling, which suggests its regulatory role in immune response. Two alternatively spliced transcript variants of this gene encoding the same protein have been reported. [provided by RefSeq, Jul 2008]
Expression
Biased expression in bone marrow (RPKM 25.4), spleen (RPKM 6.1) and 8 other tissues See more
Orthologs
mouse all
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Genomic context

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See RELT in Genome Data Viewer
Location:
11q13.4
Exon count:
12
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (73376399..73397474)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (73305536..73326611)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (73087444..73108519)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3737 Neighboring gene ARHGEF17 antisense RNA 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:73019433-73020310 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73020316-73021136 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5234 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73031799-73032452 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:73032453-73033105 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:73033106-73033758 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73036372-73037023 Neighboring gene Rho guanine nucleotide exchange factor 17 Neighboring gene Sharpr-MPRA regulatory region 2623 Neighboring gene uncharacterized LOC124902710 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73044313-73045026 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73061599-73062100 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:73073093-73073599 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5235 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3740 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3741 Neighboring gene Sharpr-MPRA regulatory region 2034 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3742 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5236 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3743 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73097219-73098168 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73098169-73099116 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:73099117-73100064 Neighboring gene family with sequence similarity 168 member A Neighboring gene MPRA-validated peak1349 silencer Neighboring gene MPRA-validated peak1350 silencer Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73166211-73166710 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr11:73205355-73205873 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:73205874-73206391 Neighboring gene NANOG hESC enhancer GRCh37_chr11:73262685-73263225 Neighboring gene ReSE screen-validated silencer GRCh37_chr11:73264745-73264969 Neighboring gene Sharpr-MPRA regulatory region 14801 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:73308491-73309219 Neighboring gene high mobility group nucleosomal binding domain 2 pseudogene 38 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3745 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73336706-73337222 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:73337223-73337737 Neighboring gene MIA SH3 domain ER export factor 2 pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. New missense variants in RELT causing hypomineralised amelogenesis imperfecta. Nikolopoulos G, et al. Clin Genet, 2020 May. PMID 32052416, Free PMC Article
  2. RELT promotes the growth of esophageal squamous cell carcinoma by activating the NF-κB pathway. Yao W, et al. Cell Cycle, 2021 Jul. PMID 34121605, Free PMC Article
  3. RELT, a new member of the tumor necrosis factor receptor superfamily, is selectively expressed in hematopoietic tissues and activates transcription factor NF-kappaB. Sica GL, et al. Blood, 2001 May 1. PMID 11313261
  4. Interactions of tumor necrosis factor (TNF) and TNF receptor family members in the mouse and human. Bossen C, et al. J Biol Chem, 2006 May 19. PMID 16547002
  5. TRAIL-induced cleavage and inactivation of SPAK sensitizes cells to apoptosis. Polek TC, et al. Biochem Biophys Res Commun, 2006 Oct 27. PMID 16950202

See all (26) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. RELT promotes the growth of esophageal squamous cell carcinoma by activating the NF-kappaB pathway.
    Title: RELT promotes the growth of esophageal squamous cell carcinoma by activating the NF-κB pathway.
  2. New missense variants in RELT causing hypomineralised amelogenesis imperfecta.
    Title: New missense variants in RELT causing hypomineralised amelogenesis imperfecta.
  3. Collectively, this study provides more insights into RELT expression, RELT family member function, and the mechanism of RELT-induced death.
    Title: RELT family members activate p38 and induce apoptosis by a mechanism distinct from TNFR1.
  4. report that overexpression of RELT or its homologues RELL1 and RELL2 in HEK 293 epithelial cells results in cell death with morphological characteristics consistent with the activation of an apoptotic pathway.
    Title: RELT induces cellular death in HEK 293 epithelial cells.
  5. Receptor expressed in lymphoid tissue (RELT) and its novel homologues RELL1 and RELL2 co-localize with one another at the plasma membrane.
    Title: Identification of RELT homologues that associate with RELT and are phosphorylated by OSR1.
Submit: New GeneRIF Correction

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description Tests
Amelogenesis imperfecta, type 3C
MedGen: C5193069 OMIM: 618386 GeneReviews: Not available
not available

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

HIV-1 interactions

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Replication interactions

Interaction Pubs
HIV-1 infection (VSV-G pseudotyped) of CEMT4 T cells downregulates plasma membrane expression of RELT PubMed

Go to the HIV-1, Human Interaction Database

Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Clone Names

  • FLJ14993

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
Process Evidence Code Pubs
involved_in amelogenesis IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in amelogenesis IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in apoptotic process IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in apoptotic process IMP
Inferred from Mutant Phenotype
more info
 PubMed 
Component Evidence Code Pubs
located_in nucleoplasm IDA
Inferred from Direct Assay
more info
  
located_in perinuclear region of cytoplasm IEA
Inferred from Electronic Annotation
more info
  
located_in plasma membrane IEA
Inferred from Electronic Annotation
more info
  

General protein information

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Preferred Names
tumor necrosis factor receptor superfamily member 19L
Names
RELT tumor necrosis factor receptor
receptor expressed in lymphoid tissues

NCBI Reference Sequences (RefSeq)

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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_001425248.1 → NP_001412177.1  tumor necrosis factor receptor superfamily member 19L isoform 2 precursor

    Status: REVIEWED

    Source sequence(s)
    AP000562, AP000763

  2. NM_001425249.1 → NP_001412178.1  tumor necrosis factor receptor superfamily member 19L isoform 3 precursor

    Status: REVIEWED

    Source sequence(s)
    AP000562, AP000763

  3. NM_001425250.1 → NP_001412179.1  tumor necrosis factor receptor superfamily member 19L isoform 4 precursor

    Status: REVIEWED

    Source sequence(s)
    AP000562, AP000763

  4. NM_001425251.1 → NP_001412180.1  tumor necrosis factor receptor superfamily member 19L isoform 5

    Status: REVIEWED

    Source sequence(s)
    AP000562, AP000763

  5. NM_001425252.1 → NP_001412181.1  tumor necrosis factor receptor superfamily member 19L isoform 6 precursor

    Status: REVIEWED

    Source sequence(s)
    AP000562, AP000763

  6. NM_001425253.1 → NP_001412182.1  tumor necrosis factor receptor superfamily member 19L isoform 7 precursor

    Status: REVIEWED

    Source sequence(s)
    AP000562, AP000763

  7. NM_032871.4 → NP_116260.2  tumor necrosis factor receptor superfamily member 19L isoform 1 precursor

    See identical proteins and their annotated locations for NP_116260.2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) differs in the 5' UTR compared to variant 2. Both variants encode the same protein.
    Source sequence(s)
    AP000562, AP000763
    Consensus CDS
    CCDS8222.1
    UniProtKB/Swiss-Prot
    Q86V34, Q969Z4, Q96JU1, Q9BUX7
    Related
    ENSP00000377207.2, ENST00000393580.2
    Conserved Domains (2) summary
    cd13419
    Location:27 → 112
    TNFRSF19L; tumor necrosis factor receptor superfamily member 19-like (TNFRSF19L), also known as receptor expressed in lymphoid tissues (RELT)
    pfam12606
    Location:163 → 198
    RELT; tumor necrosis factor receptor superfamily member 19

  8. NM_152222.2 → NP_689408.1  tumor necrosis factor receptor superfamily member 19L isoform 1 precursor

    See identical proteins and their annotated locations for NP_689408.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Both variants encode the same protein.
    Source sequence(s)
    AP000562, AP000763
    Consensus CDS
    CCDS8222.1
    UniProtKB/Swiss-Prot
    Q86V34, Q969Z4, Q96JU1, Q9BUX7
    Related
    ENSP00000064780.2, ENST00000064780.7
    Conserved Domains (2) summary
    cd13419
    Location:27 → 112
    TNFRSF19L; tumor necrosis factor receptor superfamily member 19-like (TNFRSF19L), also known as receptor expressed in lymphoid tissues (RELT)
    pfam12606
    Location:163 → 198
    RELT; tumor necrosis factor receptor superfamily member 19

RNA

  1. NR_189151.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AP000562, AP000763

  2. NR_189152.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AP000562, AP000763

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    73376399..73397474
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_047427757.1 → XP_047283713.1  tumor necrosis factor receptor superfamily member 19L isoform X1

  2. XM_047427759.1 → XP_047283715.1  tumor necrosis factor receptor superfamily member 19L isoform X3

  3. XM_047427760.1 → XP_047283716.1  tumor necrosis factor receptor superfamily member 19L isoform X4

  4. XM_047427761.1 → XP_047283717.1  tumor necrosis factor receptor superfamily member 19L isoform X5

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    73305536..73326611
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054370265.1 → XP_054226240.1  tumor necrosis factor receptor superfamily member 19L isoform X1

  2. XM_054370267.1 → XP_054226242.1  tumor necrosis factor receptor superfamily member 19L isoform X3

  3. XM_054370268.1 → XP_054226243.1  tumor necrosis factor receptor superfamily member 19L isoform X4

  4. XM_054370269.1 → XP_054226244.1  tumor necrosis factor receptor superfamily member 19L isoform X5

Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q969Z4.1 GenPept UniProtKB/Swiss-Prot:Q969Z4

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