Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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ID History
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Gene: Snapc1 ENSRNOG00000009296

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Description

small nuclear RNA activating complex, polypeptide 1 [Source:RGD Symbol;Acc:1304671]

Gene Synonyms

LOC314228

Location

Primary_assembly 6: 98,420,340-98,442,489 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 2 transcripts (splice variants) and 252 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000136686.1	Snapc1-202	2370	420aa	ENSRNOP00000107314.1	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,
ENSRNOT00000012361.7	Snapc1-201	1357	420aa	ENSRNOP00000012361.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7ES94	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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