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: TBC1D22B ENSSSCG00000001577

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Description

TBC1 domain family member 22B [Source:VGNC Symbol;Acc:VGNC:93771]

Location

Primary_assembly 7: 32,839,257-32,914,402 forward strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 1 transcript (splice variant), 207 orthologues and 34 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000058002.3	TBC1D22B-201	3324	486aa	ENSSSCP00000048308.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AWN3 A0A8D1CK27	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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