Description

keratin 20, type I [Source:HGNC Symbol;Acc:HGNC:20412]

Synonyms

CK20, K20, MGC35423

Location

Chromosome 17: 40,875,941-40,885,227 reverse strand.

View alleles of this gene on alternate assemblies

INSDC coordinates

chromosome:GRCh38:CM000679.2:40875941:40885227:1

About this gene

This gene has 2 transcripts (splice variants), 1 gene allele, 53 orthologues, 4 paralogues, is a member of 1 Ensembl protein family and is associated with 68 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
KRT20-001ENST000001675881737424aaENSP00000167588
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS11379P35900 NM_019010
NP_061883
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.

KRT20-002ENST00000482529307No protein-
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
---TSL:2

Transcript Support Level 2, when transcripts are supported by multiple ESTs or by an mRNA flagged as suspect.

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.

Gene-based displays