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

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Gene: ZNF566 ENSBTAG00000031686

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Description

zinc finger protein 566 [Source:VGNC Symbol;Acc:VGNC:37303]

Location

Primary_assembly 18: 47,044,071-47,084,182 forward strand.

ARS-UCD1.3:CM008185.2

About this gene

This gene has 4 transcripts (splice variants), 157 orthologues and 35 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000134030.1	ZNF566-204	2330	452aa	ENSBTAP00000094203.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000126969.1	ZNF566-201	2426	392aa	ENSBTAP00000091077.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000006397.7	ZNF566-202	2364	387aa	ENSBTAP00000006397.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q2KJ67	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,
ENSBTAT00000122612.1	ZNF566-203	1570	386aa	ENSBTAP00000088633.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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