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: Cldn19 ENSRNOG00000007922

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Description

claudin 19 [Source:RGD Symbol;Acc:1305000]

Gene Synonyms

LOC298487

Location

Primary_assembly 5: 138,148,501-138,155,666 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 3 transcripts (splice variants), 203 orthologues, 30 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000047151.4	Cldn19-201	1834	224aa	ENSRNOP00000050261.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5QT56-1	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,
ENSRNOT00000128074.1	Cldn19-203	4062	211aa	ENSRNOP00000099622.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JZM5	-
ENSRNOT00000113733.2	Cldn19-202	1816	218aa	ENSRNOP00000080206.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5QT56-2	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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