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
- 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: BTBD6 ENSPTRG00000052248

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Description

BTB domain containing 6 [Source:VGNC Symbol;Acc:VGNC:58541]

Location

Chromosome 14: 90,625,253-90,627,777 forward strand.

Pan_tro_3.0:CM000328.3

About this gene

This gene has 1 transcript (splice variant), 269 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000086758.1	BTBD6-201	2174	485aa	ENSPTRP00000066757.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2Y9A9 K7B3U3	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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