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

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Gene: tnrc6b ENSDARG00000074161

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Description

trinucleotide repeat containing adaptor 6B [Source:ZFIN;Acc:ZDB-GENE-030131-13]

Gene Synonyms

fa01f05, fb21h03, fc23h10, hm:zeh0114, im:6968518, wu:fa01f05, wu:fb21h03, wu:fc23h10

Location

Chromosome 12: 19,281,189-19,301,988 forward strand.

GRCz11:CM002896.2

About this gene

This gene has 1 transcript (splice variant), 213 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000153428.2	tnrc6b-201	7867	1984aa	ENSDARP00000127361.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	U3JAU2	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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