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
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RNASEL ENSSSCG00000015549

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Description

ribonuclease L [Source:NCBI gene (formerly Entrezgene);Acc:100048946]

Location

Primary_assembly 9: 123,893,294-123,910,398 reverse strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 2 transcripts (splice variants) and 128 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000035305.4	RNASEL-201	4675	743aa	ENSSSCP00000053969.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZPJ7 A0A4X1U1A2	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,
ENSSSCT00000094073.1	RNASEL-202	2614	644aa	ENSSSCP00000075646.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4F8E7	-

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Summary

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