Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Dgcr6 ENSRNOG00000001880

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Description

DiGeorge syndrome critical region 6 [Source:RGD Symbol;Acc:1309390]

Gene Synonyms

LOC303794

Location

Primary_assembly 11: 96,432,024-96,437,255 reverse strand.

GRCr8:CM070401.1

About this gene

This gene has 2 transcripts (splice variants), 213 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000102550.2	Dgcr6-202	1264	229aa	ENSRNOP00000096660.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AQQ6	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,
ENSRNOT00000002574.8	Dgcr6-201	1022	201aa	ENSRNOP00000002574.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FP83	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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