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

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Gene: CLDN7 ENSSSCG00000017934

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Description

claudin 7 [Source:VGNC Symbol;Acc:VGNC:97930]

Location

Primary_assembly 12: 52,612,510-52,628,362 reverse strand.

Sscrofa11.1:CM000823.5

About this gene

This gene has 2 transcripts (splice variants), 161 orthologues and 29 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000019518.5	CLDN7-201	1286	211aa	ENSSSCP00000019000.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1VE38 C3VPJ4	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,
ENSSSCT00000028238.3	CLDN7-202	864	146aa	ENSSSCP00000025602.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1CJ87 I3LNC8	-

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Summary

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