Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: Espnl ENSRNOG00000024717

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Description

espin-like [Source:RGD Symbol;Acc:1562432]

Gene Synonyms

LOC301606, RGD1562432

Location

Primary_assembly 9: 99,359,578-99,384,342 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 2 transcripts (splice variants), 201 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000033629.7	Espnl-201	4522	999aa	ENSRNOP00000036626.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZGJ2	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,
ENSRNOT00000119788.2	Espnl-202	4387	954aa	ENSRNOP00000083486.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GAU1	-

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Summary

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