Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SNRPC ENSBTAG00000024549

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Description

small nuclear ribonucleoprotein polypeptide C [Source:VGNC Symbol;Acc:VGNC:35078]

Location

Primary_assembly 23: 8,784,897-8,795,967 forward strand.

ARS-UCD2.0:CM008190.2

About this gene

This gene has 3 transcripts (splice variants) and 179 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000034155.5	SNRPC-203	1014	180aa	ENSBTAP00000034056.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6ZC43	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,
ENSBTAT00000080221.3	SNRPC-202	1168	178aa	ENSBTAP00000065451.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M5A1	-
ENSBTAT00000141248.1	SNRPC-201	1020	159aa	ENSBTAP00000106433.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q32PA0	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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