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
External references
Supporting evidence
ID History
- Gene history

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Gene: Zfand2a ENSRNOG00000032917

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Description

zinc finger AN1-type containing 2A [Source:RGD Symbol;Acc:1310991]

Gene Synonyms

LOC360772, MGC94876, RGD1310991

Location

Primary_assembly 12: 20,275,450-20,286,513 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants), 123 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000047634.5	Zfand2a-201	3194	171aa	ENSRNOP00000043105.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QLB5 A6K1V4	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,
ENSRNOT00000083814.3	Zfand2a-202	3064	155aa	ENSRNOP00000069561.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5U2P3	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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