Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: SETD6 ENSPTRG00000008182

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Description

SET domain containing 6, protein lysine methyltransferase [Source:VGNC Symbol;Acc:VGNC:5917]

Location

Chromosome 16: 49,204,939-49,210,491 forward strand.

Pan_tro_3.0:CM000330.3

About this gene

This gene has 2 transcripts (splice variants), 194 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000096947.1	SETD6-201	3497	474aa	ENSPTRP00000064687.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RJ48 A0A6D2WC98	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, APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. 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 P5,
ENSPTRT00000015086.5	SETD6-202	3421	449aa	ENSPTRP00000013971.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XUX6 H2QB86	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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