Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Slfn5 ENSRNOG00000021719

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Description

schlafen family member 5 [Source:RGD Symbol;Acc:1312025]

Gene Synonyms

LOC303377

Location

Primary_assembly 10: 68,378,449-68,392,544 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 86 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000076445.4	Slfn5-202	6134	940aa	ENSRNOP00000068390.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MK60	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,
ENSRNOT00000035730.8	Slfn5-201	3138	866aa	ENSRNOP00000037767.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LX81	-

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Summary

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