Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SETBP1 ENSDARG00000093799

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Description

SET binding protein 1 [Source:HGNC Symbol;Acc:HGNC:15573]

Location

Chromosome 5: 52,039,067-52,132,978 forward strand.

GRCz11:CM002889.2

About this gene

This gene has 2 transcripts (splice variants), 227 orthologues and 35 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000143276.3	SETBP1-201	4966	1438aa	ENSDARP00000112840.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0R147	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000166902.2	SETBP1-202	4609	1438aa	ENSDARP00000133167.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0R147	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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