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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: CLDN2 ENSG00000165376

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Description

claudin 2 [Source:HGNC Symbol;Acc:2041]

Location

Chromosome X: 106,143,394-106,174,091 forward strand.

GRCh37:CM000685.1

About this gene

This gene has 3 transcripts (splice variants) and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000541806.1	CLDN2-202	3150	230aa	ENSP00000441283.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS14524	P57739	NM_001171092.1	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000336803.1	CLDN2-001	2959	230aa	ENSP00000336571.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS14524	P57739	NM_020384.3	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000540876.1	CLDN2-201	2919	230aa	ENSP00000443230.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS14524	P57739	NM_001171095.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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