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

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Gene: DDRGK1 ENSBTAG00000013753

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Description

DDRGK domain containing 1 [Source:VGNC Symbol;Acc:VGNC:27954]

Location

Primary_assembly 13: 52,002,925-52,014,801 forward strand.

ARS-UCD2.0:CM008180.2

About this gene

This gene has 4 transcripts (splice variants) and 170 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000123807.2	DDRGK1-204	1436	319aa	ENSBTAP00000084189.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SK08	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000099531.2	DDRGK1-201	1340	287aa	ENSBTAP00000090160.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SXR6	-
ENSBTAT00000018273.5	DDRGK1-202	1275	313aa	ENSBTAP00000018273.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MK36	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSBTAT00000072069.3	DDRGK1-203	1200	288aa	ENSBTAP00000066136.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LZ83	-

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Summary

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