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
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: Csrnp2 ENSRNOG00000019653

.

Description

cysteine and serine rich nuclear protein 2 [Source:RGD Symbol;Acc:1308916]

Gene Synonyms

Csnrp2, LOC315308, RGD1308916

Location

Primary_assembly 7: 133,473,027-133,488,868 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 1 transcript (splice variant), 197 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000026613.6	Csrnp2-201	4544	535aa	ENSRNOP00000026613.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KCK1 D4A1W4	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,

.

Summary

.

.