Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: CLDN8 ENSSSCG00000012030

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Description

claudin 8 [Source:NCBI gene (formerly Entrezgene);Acc:100302021]

Location

Primary_assembly 13: 193,562,074-193,564,168 reverse strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 1 transcript (splice variant), 222 orthologues and 29 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000013162.3	CLDN8-201	2095	225aa	ENSSSCP00000012812.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U9B9 F1SHM7	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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