Human (GRCh38.p14)
Description

TNF receptor associated factor 7 [Source:HGNC Symbol;Acc:HGNC:20456]

Gene Synonyms

DKFZP586I021, MGC7807, RFWD1, RNF119

Location

Chromosome 16: 2,155,698-2,178,129 forward strand.

GRCh38:CM000678.2

About this gene

This gene has 9 transcripts (splice variants), 196 orthologues, 14 paralogues and is associated with 73 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000326181.11TRAF7-2013683670aaENSP00000318944.6
 
Protein coding
CCDS10461Q6Q0C0-1 NM_032271.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000565383.5TRAF7-20379954aaENSP00000479297.1
 
Protein coding
H3BUP4 -GENCODE basicTSL:5
ENST00000567645.2TRAF7-204737147aaENSP00000456034.1
 
Protein coding
H3BR17 -TSL:5CDS 3' incomplete
ENST00000567653.5TRAF7-20566686aaENSP00000478515.1
 
Protein coding
A0A087WUB0 -GENCODE basicTSL:2
ENST00000704452.1TRAF7-2082886670aaENSP00000515903.1
 
Nonsense mediated decay
CCDS10461Q6Q0C0-1 --
ENST00000704453.1TRAF7-2092681589aaENSP00000515904.1
 
Nonsense mediated decay
A0A994J4N1 -CDS 5' incomplete
ENST00000564067.5TRAF7-20287454aaENSP00000457735.1
 
Nonsense mediated decay
H3BUP4 -TSL:3
ENST00000569686.5TRAF7-206586No protein-
 
Retained intron
--TSL:2
ENST00000570169.1TRAF7-207411No protein-
 
Retained intron
--TSL:3