Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ARID4B ENSSSCG00000060488

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Description

AT-rich interaction domain 4B [Source:HGNC Symbol;Acc:HGNC:15550]

Location

Primary_assembly 14: 55,924,367-56,082,198 forward strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 1 transcript (splice variant), 219 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000053189.2	ARID4B-201	5764	1225aa	ENSSSCP00000057958.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BN71 A0A8D0NSA0	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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