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: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: ZNF214 ENSBTAG00000020289

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Description

zinc finger protein 214 [Source:VGNC Symbol;Acc:VGNC:49994]

Location

Primary_assembly 15: 45,721,955-45,745,075 forward strand.

ARS-UCD2.0:CM008182.2

About this gene

This gene has 4 transcripts (splice variants), 70 orthologues and 34 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000127685.1	ZNF214-201	3144	802aa	ENSBTAP00000089791.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SWU7	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,
ENSBTAT00000125368.1	ZNF214-203	3127	605aa	ENSBTAP00000099200.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TQ99	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,
ENSBTAT00000027039.7	ZNF214-202	2382	576aa	ENSBTAP00000027039.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3X7G3	-
ENSBTAT00000151152.1	ZNF214-204	2073	560aa	ENSBTAP00000105445.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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