Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: CLDN11 ENSBTAG00000019060

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Description

claudin 11 [Source:VGNC Symbol;Acc:VGNC:53517]

Location

Primary_assembly 1: 96,999,963-97,014,866 reverse strand.

ARS-UCD2.0:CM008168.2

About this gene

This gene has 2 transcripts (splice variants), 261 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000087526.1	CLDN11-202	1927	242aa	ENSBTAP00000093160.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T8M7	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,
ENSBTAT00000025374.4	CLDN11-201	1874	208aa	ENSBTAP00000025374.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MI16	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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