Human Gene TNFRSF25 (ENST00000356876.8_10) from GENCODE V47lift37
  Description: TNF receptor superfamily member 25, transcript variant 2 (from RefSeq NM_003790.3)
Gencode Transcript: ENST00000356876.8_10
Gencode Gene: ENSG00000215788.11_19
Transcript (Including UTRs)
   Position: hg19 chr1:6,520,846-6,526,233 Size: 5,388 Total Exon Count: 10 Strand: -
Coding Region
   Position: hg19 chr1:6,521,494-6,526,167 Size: 4,674 Coding Exon Count: 10 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
GO AnnotationsmRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr1:6,520,846-6,526,233)mRNA (may differ from genome)Protein (417 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsHGNC
MalacardsMGIOMIMPubMedReactomeUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: TNR25_HUMAN
DESCRIPTION: RecName: Full=Tumor necrosis factor receptor superfamily member 25; AltName: Full=Apo-3; AltName: Full=Apoptosis-inducing receptor AIR; AltName: Full=Apoptosis-mediating receptor DR3; AltName: Full=Apoptosis-mediating receptor TRAMP; AltName: Full=Death receptor 3; AltName: Full=Lymphocyte-associated receptor of death; Short=LARD; AltName: Full=Protein WSL; AltName: Full=Protein WSL-1; Flags: Precursor;
FUNCTION: Receptor for TNFSF12/APO3L/TWEAK. Interacts directly with the adapter TRADD. Mediates activation of NF-kappa-B and induces apoptosis. May play a role in regulating lymphocyte homeostasis.
SUBUNIT: Homodimer. Interacts strongly via the death domains with TNFRSF1 and TRADD to activate at least two distinct signaling cascades, apoptosis and NF-kappa-B signaling. Interacts with BAG4.
SUBCELLULAR LOCATION: Isoform 1: Cell membrane; Single-pass type I membrane protein.
SUBCELLULAR LOCATION: Isoform 2: Cell membrane; Single-pass type I membrane protein.
SUBCELLULAR LOCATION: Isoform 9: Cell membrane; Single-pass type I membrane protein.
SUBCELLULAR LOCATION: Isoform 11: Cell membrane; Single-pass type I membrane protein.
SUBCELLULAR LOCATION: Isoform 3: Secreted.
SUBCELLULAR LOCATION: Isoform 4: Secreted.
SUBCELLULAR LOCATION: Isoform 5: Secreted.
SUBCELLULAR LOCATION: Isoform 6: Secreted.
SUBCELLULAR LOCATION: Isoform 7: Secreted.
SUBCELLULAR LOCATION: Isoform 8: Secreted.
SUBCELLULAR LOCATION: Isoform 10: Secreted.
SUBCELLULAR LOCATION: Isoform 12: Secreted.
TISSUE SPECIFICITY: Abundantly expressed in thymocytes and lymphocytes. Detected in lymphocyte-rich tissues such as thymus, colon, intestine, and spleen. Also found in the prostate.
PTM: Glycosylated (Probable).
SIMILARITY: Contains 1 death domain.
SIMILARITY: Contains 4 TNFR-Cys repeats.
WEB RESOURCE: Name=NIEHS-SNPs; URL="http://egp.gs.washington.edu/data/tnfrsf25/";

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: TNFRSF25
Diseases sorted by gene-association score: diabetes mellitus, insulin-dependent, 18 (10), haemophilus meningitis (10), diabetes mellitus, insulin-dependent, 17 (9), punctate epithelial keratoconjunctivitis (9), autoimmune disease of gastrointestinal tract (8), juvenile dermatitis herpetiformis (8), heart block, congenital (8), superficial keratitis (7), adrenal cortical hypofunction (7), herpes gestationis (7), autoimmune disease of endocrine system (7), jejunal adenocarcinoma (7), childhood type dermatomyositis (6), diffuse scleroderma (6), adie pupil (6), diabetes mellitus, insulin-dependent, 2 (6), autoimmune disease of skin and connective tissue (6), diabetes mellitus, insulin-dependent, 11 (6), immunoglobulin alpha deficiency (6), diabetes mellitus, insulin-dependent, 5 (5), hypersensitivity reaction disease (5), malignant essential hypertension (5), ascending cholangitis (5), toxic diffuse goiter (4), neuromuscular junction disease (4), diabetes mellitus, insulin-dependent (2), immune system disease (1), cholangitis, primary sclerosing (1), glucose metabolism disease (1)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 158.76 RPKM in Brain - Cerebellum
Total median expression: 746.01 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -25.2066-0.382 Picture PostScript Text
3' UTR -251.70648-0.388 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR000488 - Death
IPR011029 - DEATH-like
IPR001368 - TNFR/NGFR_Cys_rich_reg
IPR022329 - TNFR_25

Pfam Domains:
PF00020 - TNFR/NGFR cysteine-rich region
PF00531 - Death domain

SCOP Domains:
47986 - DEATH domain
57586 - TNF receptor-like
57184 - Growth factor receptor domain

ModBase Predicted Comparative 3D Structure on Q93038
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The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
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-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005031 tumor necrosis factor-activated receptor activity
GO:0038023 signaling receptor activity

Biological Process:
GO:0006915 apoptotic process
GO:0006954 inflammatory response
GO:0006955 immune response
GO:0007165 signal transduction
GO:0007166 cell surface receptor signaling pathway
GO:0007275 multicellular organism development
GO:0032496 response to lipopolysaccharide
GO:0033209 tumor necrosis factor-mediated signaling pathway
GO:0042127 regulation of cell proliferation
GO:0042981 regulation of apoptotic process
GO:0097190 apoptotic signaling pathway

Cellular Component:
GO:0005576 extracellular region
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane


-  Descriptions from all associated GenBank mRNAs
  AB018263 - Homo sapiens KIAA0720 mRNA for KIAA0720 protein.
AK226112 - Homo sapiens mRNA for ATP-binding cassette, sub-family A, member 2 isoform a variant, clone: hg01099.
U75380 - Human apoptosis-mediating receptor TRAMP mRNA, partial cds.
AY358309 - Homo sapiens clone DNA58801 DR3 (UNQ455) mRNA, complete cds.
U83597 - Human death domain receptor 3 (DDR3) mRNA, partial cds.
AK094488 - Homo sapiens cDNA FLJ37169 fis, clone BRACE2027770, highly similar to WSL-1 PROTEIN PRECURSOR.
AK094463 - Homo sapiens cDNA FLJ37144 fis, clone BRACE2024610, highly similar to Tumor necrosis factor receptor superfamily member 25 precursor.
U74611 - Human Apo-3 mRNA, complete cds.
AF026070 - Homo sapiens death receptor 3 beta (DR3) mRNA, complete cds.
AF026071 - Homo sapiens soluble death receptor 3 beta (DR3) mRNA, complete cds.
Y09392 - H.sapiens mRNA for WSL-LR, WSL-S1 and WSL-S2 proteins.
BC117189 - Homo sapiens tumor necrosis factor receptor superfamily, member 25, mRNA (cDNA clone MGC:150798 IMAGE:40125740), complete cds.
BC143886 - Homo sapiens tumor necrosis factor receptor superfamily, member 25, mRNA (cDNA clone MGC:177419 IMAGE:9052402), complete cds.
JD151786 - Sequence 132810 from Patent EP1572962.
JD121753 - Sequence 102777 from Patent EP1572962.
JD458929 - Sequence 439953 from Patent EP1572962.
JD327061 - Sequence 308085 from Patent EP1572962.
U72763 - Human death receptor 3 (DR3) mRNA, complete cds.
U78029 - Human aoptosis inducing receptor AIR mRNA, complete cds.
U94501 - Human lymphocyte associated receptor of death 1a mRNA, complete cds.
U94502 - Human lymphocyte associated receptor of death 1b mRNA, alternatively spliced, complete cds.
U94503 - Human lymphocyte associated receptor of death 2 mRNA, alternatively spliced, complete cds.
U94504 - Human lymphocyte associated receptor of death 3 mRNA, alternatively spliced, complete cds.
U94505 - Human lymphocyte associated receptor of death 4 mRNA, alternatively spliced, complete cds.
U94506 - Human lymphocyte associated receptor of death 5 mRNA, alternatively spliced, complete cds.
U94507 - Human lymphocyte associated receptor of death 6 mRNA, alternatively spliced, complete cds.
U94508 - Human lymphocyte associated receptor of death 7 mRNA, alternatively spliced, complete cds.
U94509 - Human lymphocyte associated receptor of death 8 mRNA, alternatively spliced, complete cds.
U94510 - Human lymphocyte associated receptor of death 9 mRNA, alternatively spliced, complete cds.
JD175084 - Sequence 156108 from Patent EP1572962.
HQ258574 - Synthetic construct Homo sapiens clone IMAGE:100073099 tumor necrosis factor receptor superfamily, member 25 (TNFRSF25), transcript variant 2 (TNFRSF25) gene, encodes complete protein.
AB590587 - Synthetic construct DNA, clone: pFN21AE1895, Homo sapiens TNFRSF25 gene for tumor necrosis factor receptor superfamily, member 25, without stop codon, in Flexi system.
JD443569 - Sequence 424593 from Patent EP1572962.
JD479840 - Sequence 460864 from Patent EP1572962.
JD058270 - Sequence 39294 from Patent EP1572962.
JD258696 - Sequence 239720 from Patent EP1572962.
JD456560 - Sequence 437584 from Patent EP1572962.
JD106346 - Sequence 87370 from Patent EP1572962.
AB308321 - Homo sapiens TNFRSF25 mRNA for tumor necrosis factor receptor superfamily member 25 deletion mutant, complete cds.
U83598 - Human death domain receptor 3 soluble form (DDR3) mRNA, partial cds.
U75381 - Human apoptosis-mediating receptor TRAMP ex mRNA, alternatively spliced, partial cds.
U94512 - Human lymphocyte associated receptor of death 11 mRNA, alternatively spliced, partial cds.
U83600 - Human death domain receptor 3 (DDR3) mRNA, alternatively spliced form 2, partial cds.
U94511 - Human lymphocyte associated receptor of death 10 pseudogene, partial sequence.
AK131074 - Homo sapiens mRNA for FLJ00260 protein.

-  Biochemical and Signaling Pathways
  BioCarta from NCI Cancer Genome Anatomy Project
h_deathPathway - Induction of apoptosis through DR3 and DR4/5 Death Receptors

Reactome (by CSHL, EBI, and GO)

Protein Q93038 (Reactome details) participates in the following event(s):

R-HSA-5693012 TNFSF15 binds TNFRSF25
R-HSA-5669034 TNFs bind their physiological receptors
R-HSA-5668541 TNFR2 non-canonical NF-kB pathway
R-HSA-1280215 Cytokine Signaling in Immune system
R-HSA-168256 Immune System

-  Other Names for This Gene
  Alternate Gene Symbols: APO3, B1ALX2, B1ALX3, B7ZLL7, DDR3, DR3, ENST00000356876.1, ENST00000356876.2, ENST00000356876.3, ENST00000356876.4, ENST00000356876.5, ENST00000356876.6, ENST00000356876.7, NM_003790, O00275, O00276, O00277, O00278, O00279, O00280, O14865, O14866, P78507, P78515, Q17RU4, Q92983, Q93036, Q93037, Q93038, Q99722, Q99830, Q99831, Q9BY86, Q9UME0, Q9UME1, Q9UME5, TNFRSF12, TNR25_HUMAN, uc317zts.1, uc317zts.2, UNQ455/PRO779, WSL, WSL1
UCSC ID: ENST00000356876.8_10
RefSeq Accession: NM_003790.3
Protein: Q93038 (aka TNR25_HUMAN or TR25_HUMAN)

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.