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
  - 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: DGCR6L ENSBTAG00000047299

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Description

DiGeorge syndrome critical region 6 like [Source:NCBI gene (formerly Entrezgene);Acc:100126445]

Gene Synonyms

DGCR6

Location

Primary_assembly 17: 73,122,983-73,128,212 reverse strand.

ARS-UCD2.0:CM008184.2

About this gene

This gene has 1 transcript (splice variant) and 212 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000065888.3	DGCR6L-201	1643	209aa	ENSBTAP00000055926.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6DLG4	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,

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Summary

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