Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Jup ENSRNOG00000015380

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Description

junction plakoglobin [Source:RGD Symbol;Acc:620412]

Location

Primary_assembly 10: 85,800,814-85,827,429 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 265 orthologues, 4 paralogues and is associated with 37 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000089933.3	Jup-202	3449	749aa	ENSRNOP00000070840.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R4T1	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 ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSRNOT00000040845.4	Jup-201	3437	745aa	ENSRNOP00000043950.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HJ29 Q6P0K8	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,

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Summary

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