Human (GRCh38.p14)
Description

TNF alpha induced protein 3 [Source:HGNC Symbol;Acc:HGNC:11896]

Gene Synonyms

A20, OTUD7C

Location

Chromosome 6: 137,867,214-137,883,314 forward strand.

GRCh38:CM000668.2

About this gene

This gene has 9 transcripts (splice variants), 203 orthologues, 2 paralogues and is associated with 70 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000612899.5TNFAIP3-2064665790aaENSP00000481570.1
 
Protein coding
CCDS5187P21580 NM_001270508.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000421450.2TNFAIP3-2034689790aaENSP00000393577.2
 
Protein coding
CCDS5187P21580 Q5VXR0 -GENCODE basicAPPRIS P1TSL:2
ENST00000433680.2TNFAIP3-2044533790aaENSP00000409845.2
 
Protein coding
CCDS5187P21580 Q5VXQ9 -GENCODE basicAPPRIS P1TSL:3
ENST00000237289.8TNFAIP3-2014432790aaENSP00000237289.4
 
Protein coding
CCDS5187P21580 -GENCODE basicAPPRIS P1TSL:1
ENST00000420009.6TNFAIP3-2023861790aaENSP00000401562.2
 
Protein coding
CCDS5187Q5VXQ8 -GENCODE basicAPPRIS P1TSL:3
ENST00000711061.1TNFAIP3-2094683108aaENSP00000518561.1
 
Nonsense mediated decay
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ENST00000698330.1TNFAIP3-208336No protein-
 
Protein coding CDS not defined
---
ENST00000698329.1TNFAIP3-2075432No protein-
 
Retained intron
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ENST00000485192.2TNFAIP3-2054966No protein-
 
Retained intron
--TSL:2