Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Ins2 ENSRNOG00000020405

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Description

insulin 2 [Source:RGD Symbol;Acc:2916]

Gene Synonyms

CP-II, LOC102549619

Location

Primary_assembly 1: 197,843,281-197,864,775 reverse strand.

mRatBN7.2:CM026974.1

About this gene

This gene has 2 transcripts (splice variants), 245 orthologues, 3 paralogues and is associated with 88 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000105489.1	Ins2-202	1642	119aa	ENSRNOP00000080277.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G4B8	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,
ENSRNOT00000027656.4	Ins2-201	446	110aa	ENSRNOP00000027656.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P01323	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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