Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: Rs1 ENSRNOG00000030434

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Description

retinoschisin 1 [Source:RGD Symbol;Acc:1642515]

Location

Primary_assembly X: 37,771,135-37,800,894 reverse strand.

GRCr8:CM070411.1

About this gene

This gene has 2 transcripts (splice variants), 172 orthologues, 1 paralogue and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000040912.6	Rs1-201	1978	224aa	ENSRNOP00000042298.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A9K3Y6U2 A7UJ12	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,
ENSRNOT00000095419.2	Rs1-202	1758	180aa	ENSRNOP00000077149.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5YC76	-

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Summary

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