Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Zfp580 ENSRNOG00000016274

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Description

zinc finger protein 580 [Source:RGD Symbol;Acc:1306892]

Gene Synonyms

LOC308336, Znf580

Location

Primary_assembly 1: 77,815,461-77,834,295 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 70 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000021772.7	Zfp580-201	687	228aa	ENSRNOP00000021772.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A235	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,
ENSRNOT00000149691.1	Zfp580-204	2050	172aa	ENSRNOP00000110675.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000127525.1	Zfp580-203	1772	172aa	ENSRNOP00000105127.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000110039.2	Zfp580-202	1482	172aa	ENSRNOP00000090245.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A911	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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Orthologues

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