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: CLDN11 ENSPTRG00000015617

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Description

claudin 11 [Source:VGNC Symbol;Acc:VGNC:1780]

Location

Chromosome 3: 174,127,275-174,430,965 forward strand.

Pan_tro_3.0:CM000317.3

About this gene

This gene has 2 transcripts (splice variants), 263 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000029118.3	CLDN11-201	2149	207aa	ENSPTRP00000026870.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XP99 G2HJH3	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,
ENSPTRT00000075759.2	CLDN11-202	498	165aa	ENSPTRP00000059865.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XXB2 H2REC9	-

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Summary

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