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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 ENSG00000164007

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Description

claudin 19 [Source:HGNC Symbol;Acc:2040]

Gene Synonyms

HOMG5

Location

Chromosome 1: 43,198,764-43,205,925 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 3 transcripts (splice variants), 12 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000296387.1	CLDN19-001	2859	224aa	ENSP00000296387.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS471	Q8N6F1	NM_148960.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000539749.1	CLDN19-201	3517	218aa	ENSP00000443229.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS53306	Q8N6F1	NM_001185117.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000372539.3	CLDN19-002	1586	211aa	ENSP00000361617.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS44125	Q8N6F1	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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