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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: CLDN9 ENSG00000213937

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Description

claudin 9 [Source:HGNC Symbol;Acc:2051]

Location

Chromosome 16: 3,062,457-3,064,506 forward strand.

GRCh37:CM000678.1

About this gene

This gene has 1 transcript (splice variant) and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000445369.2	CLDN9-001	2050	217aa	ENSP00000398017.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS10487	O95484	NM_020982.3	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,

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Summary

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