Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Espn ENSRNOG00000010270

.

Description

espin [Source:RGD Symbol;Acc:620652]

Gene Synonyms

Je

Location

Primary_assembly 5: 167,909,271-167,942,984 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 3 transcripts (splice variants), 195 orthologues, 1 paralogue and is associated with 13 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000117287.2	Espn-203	3421	871aa	ENSRNOP00000097437.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ARF5	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000116345.2	Espn-202	2419	523aa	ENSRNOP00000080896.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZQJ8	-
ENSRNOT00000013646.6	Espn-201	1058	253aa	ENSRNOP00000013645.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q63618-2	-

.

Summary

.

.