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
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Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
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Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SGF29 ENSBTAG00000016883

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Description

SAGA complex associated factor 29 [Source:VGNC Symbol;Acc:VGNC:97311]

Location

Primary_assembly 25: 26,082,046-26,123,452 forward strand.

ARS-UCD1.3:CM008192.2

About this gene

This gene has 3 transcripts (splice variants) and 196 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000112309.1	SGF29-201	1323	331aa	ENSBTAP00000100132.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000100175.1	SGF29-203	1185	299aa	ENSBTAP00000098388.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000022457.7	SGF29-202	1173	293aa	ENSBTAP00000022457.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BN74	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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