RELT - RELT TNF receptor Gene

Also Known as AI3C; TRLT; TNFRSF19L

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84957

About RELT

Cytogenetic location: 11q13.4 Genomic coordinates (GRCh38): 11:73,376,399-73,397,474 (from NCBI)

This gene has 7 transcripts (splice variants), 197 orthologues, 21 paralogues and is associated with 2 phenotypes. Biased expression in bone marrow (RPKM 25.4), spleen (RPKM 6.1) and 8 other tissues.

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]

RELT Products (2)

mRNA Protein Name
NM_032871.4 NP_116260.2 tumor necrosis factor receptor superfamily member 19L precursor
NM_152222.2 NP_689408.1 tumor necrosis factor receptor superfamily member 19L precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16530727 GOA
Biological Process GO Annotation Evidence References Source
involved in amelogenesis IMP
IMP: Inferred from mutant phenotype
30506946 GOA
involved in apoptotic process IMP
IMP: Inferred from mutant phenotype
16530727 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

RELT Protein Structure

RELT

RELT: Tumour necrosis factor receptor superfamily member 19 (163 - 204)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 430 a.a.
Protein Preferred Names Protein Names

tumor necrosis factor receptor superfamily member 19L

  • RELT tumor necrosis factor receptor

Recombinant RELT Proteins

Cat. No. Product Name Accession Purity
HY-P71258 RELT Protein, Human (HEK293, Fc) Q969Z4 (S26-A160) ≥ 90%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Amelogenesis Imperfecta, Type Iiic
  • AI3C

  • Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Recessive

  • Amelogenesis Imperfecta Type 3c

  • Amelogenesis Imperfecta, Type 3c

  • Amelogenesis Imperfecta Type Iiic

  • Autosomal Recessive Amelogenesis Imperfecta Hypocalcification Type

  • Amelogenesis Imperfecta 3c

Hypoplastic Amelogenesis Imperfecta
  • Amelogenesis Imperfecta Type 1

  • Amelogenesis Imperfecta, Hypoplastic Type

  • Amelogenesis Imperfecta Local Hypoplastic Form

Amelogenesis Imperfecta
  • Ai

  • Congenital Enamel Hypoplasia

  • Al - [Amelogenesis Imperfecta]

Myopathy, Congenital, Compton-North
  • Compton-North Congenital Myopathy

  • MYPCN

  • Congenital Lethal Myopathy, Compton-North Type

Amelogenesis Imperfecta, Hypomaturation Type, Iia5
  • Amelogenesis Imperfecta Hypomaturation Type 2a5

  • AI2A5

  • Amelogenesis Imperfecta, Type Iia5

  • Amelogenesis Imperfecta Hypomaturation Type Iia5

  • Amelogenesis Imperfecta Type Iia5

  • Amelogenesis Imperfecta, Hypomaturation Type, 2a5

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
Felis catus RELT VGNC VGNC:64568
Rattus norvegicus RELT RGD RGD:1305381
Bos taurus RELT VGNC VGNC:33862
Canis familiaris RELT VGNC VGNC:45471
Mus musculus RELT MGD MGI:2443373
Macaca mulatta RELT VGNC VGNC:76728
Others RELT NCBI