Description

claudin 20 [Source:HGNC Symbol;Acc:HGNC:2042]

INSDC coordinates

chromosome:GRCh38:CM000668.2:155264013:155276548:1

About this gene

This gene has 1 transcript (splice variant), 59 orthologues, 12 paralogues, is a member of 1 Ensembl protein family and is associated with 16 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
CLDN20-001ENST000003671651209219aaENSP00000356133
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS5249P56880 NM_001001346
NP_001001346
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays