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

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Gene: cldn11b ENSDARG00000030723

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Description

claudin 11b [Source:ZFIN;Acc:ZDB-GENE-010328-13]

Gene Synonyms

cldn11, fb97c11, wu:fb97c11

Location

Chromosome 24: 26,432,541-26,441,318 forward strand.

GRCz11:CM002908.2

About this gene

This gene has 2 transcripts (splice variants), 190 orthologues and 41 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000105784.6	cldn11b-201	2843	256aa	ENSDARP00000096562.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A4QNU3	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,
ENSDART00000122554.2	cldn11b-202	1916	256aa	ENSDARP00000105607.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A4QNU3	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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