Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Cldn18 ENSRNOG00000030386

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Description

claudin 18 [Source:RGD Symbol;Acc:1359696]

Gene Synonyms

LOC315953

Location

Primary_assembly 8: 109,126,949-109,152,701 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 230 orthologues, 30 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000094503.2	Cldn18-202	1568	261aa	ENSRNOP00000087515.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5I0E5-2	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,
ENSRNOT00000052043.6	Cldn18-201	1537	261aa	ENSRNOP00000046247.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5I0E5-1	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,

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Summary

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