Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Molecular interactions
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ID History
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Gene: LOC108350036 ENSRNOG00000046421

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Description

uncharacterized LOC108350036 [Source:RGD Symbol;Acc:11487146]

Location

Primary_assembly 2: 162,820,528-162,860,116 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 1 transcript (splice variant) and 169 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000073540.4	LOC108350036-201	1537	272aa	ENSRNOP00000064553.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0R593	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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