Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: SLU7 ENSPTRG00000017491

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Description

SLU7 homolog, splicing factor [Source:VGNC Symbol;Acc:VGNC:4166]

Location

Chromosome 5: 160,739,880-160,757,800 reverse strand.

Pan_tro_3.0:CM000319.3

About this gene

This gene has 2 transcripts (splice variants) and 221 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000080531.1	SLU7-201	3796	586aa	ENSPTRP00000078898.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SPP3 A0A6D2W632	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 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,
ENSPTRT00000032341.4	SLU7-202	1713	570aa	ENSPTRP00000029882.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QRX9	-

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Summary

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