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Human (GRCh37.p13)
Description

SET nuclear oncogene [Source:HGNC Symbol;Acc:10760]

Gene Synonyms

2PP2A, I2PP2A, IGAAD, IPP2A2, PHAPII, SETP18, TAF-I, TAF-IBETA

Location

Chromosome 9: 131,445,703-131,458,679 forward strand.

GRCh37:CM000671.1

About this gene

This gene has 11 transcripts (splice variants), 12 paralogues and is associated with 42 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000372692.4SET-0012850290aaENSP00000361777.4
 
Protein coding
CCDS48037B2REB7 Q01105 Q5VXV3
NM_001287737.1Ensembl CanonicalGENCODE basic
ENST00000322030.8SET-0022915277aaENSP00000318012.8
 
Protein coding
CCDS6907Q01105 NM_003011.3GENCODE basic
ENST00000372688.4SET-2011279266aaENSP00000361773.4
 
Protein coding
CCDS59150Q01105 NM_001248001.1GENCODE basic
ENST00000372686.5SET-0101029265aaENSP00000361771.5
 
Protein coding
Q01105 --
ENST00000409104.3SET-003962268aaENSP00000387321.3
 
Protein coding
CCDS59149Q01105 NM_001248000.1GENCODE basic
ENST00000454747.1SET-00923532aaENSP00000410806.1
 
Protein coding
B2REB7 -CDS 3' incomplete
ENST00000477806.1SET-008957No protein-
 
Processed transcript
---
ENST00000466009.1SET-005597No protein-
 
Processed transcript
---
ENST00000480217.1SET-004509No protein-
 
Processed transcript
---
ENST00000485056.1SET-011483No protein-
 
Retained intron
---
ENST00000480536.1SET-012388No protein-
 
Retained intron
---

Retirement notice

Human only - retirement of this view

As of Ensembl release 93 this view will no longer be available for human, because we feel that the density of known human genetic variation is too great for the display to be informative in its current form.

Other species will not be affected, as they have less variation data.

For more information about the decision and on how to find variation data for a gene, please see our blog post.