Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: dkc1 ENSDARG00000016484

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Description

dyskeratosis congenita 1, dyskerin [Source:NCBI gene (formerly Entrezgene);Acc:613144]

Location

Chromosome 21: 43,702,010-43,716,471 forward strand.

GRCz11:CM002905.2

About this gene

This gene has 2 transcripts (splice variants), 214 orthologues and is associated with 27 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000017176.10	dkc1-201	1906	506aa	ENSDARP00000007628.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q749	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, 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,
ENSDART00000126190.4	dkc1-202	850	56aa	ENSDARP00000105779.2	Nonsense mediated decay	-	-

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Summary

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