Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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  - Orthologues
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Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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Genetic Variation
- Variant table
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- Structural variants
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Gene: Dcaf11 ENSRNOG00000018825

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Description

DDB1 and CUL4 associated factor 11 [Source:RGD Symbol;Acc:1311288]

Gene Synonyms

LOC305895, MGC109419, MGC94719, Wdr23

Location

Primary_assembly 15: 33,016,762-33,027,672 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 2 transcripts (splice variants) and 187 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000077584.3	Dcaf11-202	3182	549aa	ENSRNOP00000074435.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KH09 Q5M9G8	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,
ENSRNOT00000059987.4	Dcaf11-201	3164	543aa	ENSRNOP00000056736.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QQZ0	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,

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Summary

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