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

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Gene: CLDN2 ENSPTRG00000022156

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Description

claudin 2 [Source:HGNC Symbol;Acc:HGNC:2041]

Location

Chromosome X: 106,500,772-106,501,464 forward strand.

Pan_tro_3.0:CM000336.3

About this gene

This gene has 1 transcript (splice variant), 187 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000041255.3	CLDN2-201	693	230aa	ENSPTRP00000074471.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8K3N3 A0A6D2W7N6	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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