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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SLF1 ENSPTRG00000017079

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Description

SMC5-SMC6 complex localization factor 1 [Source:VGNC Symbol;Acc:VGNC:4165]

Location

Chromosome 5: 20,814,096-20,886,376 reverse strand.

Pan_tro_3.0:CM000319.3

About this gene

This gene has 1 transcript (splice variant), 192 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000031642.7	SLF1-201	6336	1058aa	ENSPTRP00000029231.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	K7AZ13	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,

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Summary

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