Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: DGCR6L ENSPTRG00000014080

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Description

DiGeorge syndrome critical region gene 6 like [Source:HGNC Symbol;Acc:HGNC:18551]

Location

Chromosome 22: 6,913,183-6,918,943 reverse strand.

Pan_tro_3.0:CM000335.3

About this gene

This gene has 2 transcripts (splice variants), 206 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000101645.1	DGCR6L-201	1132	220aa	ENSPTRP00000084365.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XL25 K7ANQ5	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,
ENSPTRT00000064755.2	DGCR6L-202	549	182aa	ENSPTRP00000056318.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2RBU6	-

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Summary

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