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: CLDN19 ENSBTAG00000017381

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Description

claudin 19 [Source:VGNC Symbol;Acc:VGNC:27409]

Location

Primary_assembly 3: 103,498,748-103,503,588 forward strand.

ARS-UCD1.3:CM008170.2

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000081380.2	CLDN19-202	947	224aa	ENSBTAP00000066923.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M8X0	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,
ENSBTAT00000023107.5	CLDN19-201	1660	211aa	ENSBTAP00000023107.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A7MBD3	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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