Description

tumor necrosis factor [Source:MGI Symbol;Acc:MGI:104798]

Location
INSDC coordinates

chromosome:GRCm38:CM001010.2:35199381:35202007:1

Transcripts



This gene has 2 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Tnf-001ENSMUST000000252631639235 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS28691P06804 Q0X0E6 Q3U593
Q6TDG3
NM_013693
NP_038721
TSL:1

TSL1: All splice junctions of the transcript 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 PIAPPRIS principal isoform [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Tnf-002ENSMUST000001679241462219 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS70801P06804 Q0X0E6 NM_001278601
NP_001265530
TSL:1

TSL1: All splice junctions of the transcript 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).

Gene-based displays