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

Configure this page

Share this page

Bookmark this page

.

Gene: Spetex2l1 ENSRNOG00000045737

.

Description

like [Source:RGD Symbol;Acc:1560404]

Gene Synonyms

LOC100360909, LOC302192, LOC363180, LOC501400, LOC681180, LOC691428, MGC116197, RGD1563862

Location

Primary_assembly 15: 7,096,344-7,151,696 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 1 transcript (splice variant), 131 orthologues and 201 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000048862.5	Spetex2l1-201	534	177aa	ENSRNOP00000040216.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4QQS5	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,

.

Summary

.

.