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

Configure this page

Share this page

Bookmark this page

.

Gene: cldng ENSDARG00000003701

.

Description

claudin g [Source:NCBI gene;Acc:81586]

Gene Synonyms

cb214, zgc:136312, zgc:152655

Location

Chromosome 1: 33,645,044-33,647,169 reverse strand.

GRCz11:CM002885.2

About this gene

This gene has 3 transcripts (splice variants), 21 orthologues and 41 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000015547.9	cldng-201	1075	209aa	ENSDARP00000015898.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B2GPD3 Q9YH90	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,
ENSDART00000142111.2	cldng-202	638	159aa	ENSDARP00000115881.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B8JII0	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000192758.1	cldng-203	637	209aa	ENSDARP00000153981.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B2GPD3 Q9YH90	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,

.

Summary

.

.