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

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Gene: Rcn1 ENSRNOG00000013452

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Description

reticulocalbin 1 [Source:RGD Symbol;Acc:1311292]

Gene Synonyms

LOC362182, Rcn

Location

Primary_assembly 3: 112,295,838-112,310,082 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant), 222 orthologues, 4 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000018074.8	Rcn1-201	3073	325aa	ENSRNOP00000018074.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HNW5 D3ZUB0	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,

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Summary

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