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: Rnase13 ENSRNOG00000039500

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Description

ribonuclease A family member 13 [Source:RGD Symbol;Acc:1359386]

Location

Primary_assembly 15: 27,091,441-27,152,367 reverse strand.

GRCr8:CM070405.1

About this gene

This gene has 3 transcripts (splice variants), 47 orthologues, 15 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000130070.1	Rnase13-203	4059	153aa	ENSRNOP00000099043.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000098524.2	Rnase13-202	1672	153aa	ENSRNOP00000080706.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZRB0	-
ENSRNOT00000060539.4	Rnase13-201	1384	153aa	ENSRNOP00000057279.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	R9PY04	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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