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: Snu13 ENSRNOG00000006762

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Description

small nuclear ribonucleoprotein 13 [Source:RGD Symbol;Acc:1303103]

Gene Synonyms

LOC100359574, MGC72932, Nhp2l1, Otk27

Location

Primary_assembly 7: 115,445,415-115,458,026 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 198 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000122490.1	Snu13-202	1198	144aa	ENSRNOP00000111005.1	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,
ENSRNOT00000009152.7	Snu13-201	1228	128aa	ENSRNOP00000009152.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HT44 P55770	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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