Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
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External references
Supporting evidence
ID History
- Gene history

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Gene: SGF29 ENSSSCG00000022778

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Description

SAGA complex associated factor 29 [Source:VGNC Symbol;Acc:VGNC:98315]

Location

Primary_assembly 3: 18,354,799-18,387,856 reverse strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 2 transcripts (splice variants) and 200 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000030661.4	SGF29-202	1898	328aa	ENSSSCP00000025289.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0T535 I3LMG8	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,
ENSSSCT00000044253.3	SGF29-201	1288	293aa	ENSSSCP00000043480.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AHX2 A0A4X1U8F2	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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