CLDN6 claudin 6 [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: CLDN6provided by VGNC
Official Full Name: claudin 6provided by VGNC
Primary source: VGNC:VGNC:71251
See related: Ensembl:ENSMMUG00000041201
Gene type: protein coding
RefSeq status: INFERRED
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 20

Exon count:: 2

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	20	NC_041773.1 (3079478..3082429, complement)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	20	NC_027912.1 (3909696..3913463)

Chromosome 20 - NC_041773.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

CLDN6_1604 (e-PCR)
- UniSTS:277106

CLDN6_v570 (e-PCR)
- UniSTS:277106

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables structural molecule activity	IEA Inferred from Electronic Annotation more info	PubMed

Process	Evidence Code	Pubs
involved_in bicellular tight junction assembly	IEA Inferred from Electronic Annotation more info	PubMed
involved_in cell adhesion	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in bicellular tight junction	IEA Inferred from Electronic Annotation more info	PubMed
located_in plasma membrane	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: claudin-6

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.