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: Axin2 ENSRNOG00000055010

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Description

axin 2 [Source:RGD Symbol;Acc:69259]

Gene Synonyms

axil, axin-2

Location

Primary_assembly 10: 94,395,909-94,426,575 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 3 transcripts (splice variants), 261 orthologues, 22 paralogues and is associated with 38 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000088599.3	Axin2-201	4297	838aa	ENSRNOP00000073088.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K4L4 O70240	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 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,
ENSRNOT00000108496.2	Axin2-203	4243	820aa	ENSRNOP00000091222.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AE31	-
ENSRNOT00000099900.2	Axin2-202	4102	773aa	ENSRNOP00000080393.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZPY7	APPRIS ALT1: 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 is conserved in at least 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 ALT1,

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Summary

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