Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: cldn23.1 ENSDARG00000028096

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Description

claudin 23.1 [Source:NCBI gene (formerly Entrezgene);Acc:553515]

Location

Chromosome 10: 15,046,837-15,048,781 reverse strand.

GRCz11:CM002894.2

About this gene

This gene has 2 transcripts (splice variants), 168 orthologues and 41 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000155674.3	cldn23.1-202	873	290aa	ENSDARP00000129015.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSDART00000038401.5	cldn23.1-201	1945	280aa	ENSDARP00000030329.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q6Q0	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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