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: Snapc2 ENSRNOG00000001056

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Description

small nuclear RNA activating complex, polypeptide 2 [Source:RGD Symbol;Acc:1304589]

Gene Synonyms

LOC304204

Location

Primary_assembly 12: 7,403,469-7,406,840 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants) and 167 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000001398.8	Snapc2-201	1740	376aa	ENSRNOP00000001398.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q68FX5	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,
ENSRNOT00000126086.1	Snapc2-202	1568	256aa	ENSRNOP00000106639.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KQ70	-

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Summary

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