Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: RGD1306186 ENSRNOG00000037039

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Description

similar to RIKEN cDNA 4930569K13 [Source:RGD Symbol;Acc:1306186]

Gene Synonyms

LOC298621, MGC105679

Location

Primary_assembly 5: 156,075,011-156,081,591 forward strand.

mRatBN7.2:CM026978.1

About this gene

This gene has 2 transcripts (splice variants), 665 orthologues and 45 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000033718.7	RGD1306186-201	1797	500aa	ENSRNOP00000034502.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7F487	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,
ENSRNOT00000091144.2	RGD1306186-202	1821	499aa	ENSRNOP00000069423.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5D011	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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