Description

tumor necrosis factor (ligand) superfamily, member 15 [Source:HGNC Symbol;Acc:HGNC:11931]

Synonyms

MGC129934, MGC129935, TL1, TL1A, VEGI, VEGI192A

INSDC coordinates

chromosome:GRCh38:CM000671.2:114784635:114806126:1

About this gene

This gene has 2 transcripts (splice variants), 53 orthologues, 4 paralogues, is a member of 1 Ensembl protein family and is associated with 1 phenotype.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
TNFSF15-001ENST000003740456687251aaENSP00000363157
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS6809O95150 NM_001204344
NM_005118
NP_001191273
NP_005109
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

TNFSF15-002ENST000003740442789174aaENSP00000363156
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-X6R8I9 -TSL:NA

Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

Gene-based displays