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: CLDN23 ENSPTRG00000040603

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Description

claudin 23 [Source:VGNC Symbol;Acc:VGNC:14542]

Location

Chromosome 8: 8,026,495-8,027,367 forward strand.

Pan_tro_3.0:CM000322.4

About this gene

This gene has 1 transcript (splice variant), 177 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000074927.2	CLDN23-201	873	290aa	ENSPTRP00000060615.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WKN4 H2RGG8	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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