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: ASB9 ENSPTRG00000021682

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Description

ankyrin repeat and SOCS box containing 9 [Source:VGNC Symbol;Acc:VGNC:55701]

Location

Chromosome X: 15,134,747-15,162,695 reverse strand.

Pan_tro_3.0:CM000336.3

About this gene

This gene has 1 transcript (splice variant), 129 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000040205.5	ASB9-201	1953	262aa	ENSPTRP00000045975.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8KUA9 A0A6D2W782	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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