Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Rnasek ENSRNOG00000018829

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Description

ribonuclease K [Source:RGD Symbol;Acc:1305687]

Gene Synonyms

LOC287453, RGD1305687

Location

Primary_assembly 10: 55,450,250-55,453,311 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 3 transcripts (splice variants) and 239 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000114339.2	Rnasek-203	1461	248aa	ENSRNOP00000079016.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZM61	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,
ENSRNOT00000025491.6	Rnasek-201	967	190aa	ENSRNOP00000025491.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7F776	-
ENSRNOT00000113799.2	Rnasek-202	734	157aa	ENSRNOP00000092562.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AVU2	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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