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: nr6a1b ENSDARG00000014480

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Description

nuclear receptor subfamily 6, group A, member 1b [Source:NCBI gene;Acc:497167]

Gene Synonyms

GCNF-B, si:ch211-167p9.1, zgc:114189

Location

Chromosome 21: 8,198,652-8,259,645 forward strand.

GRCz11:CM002905.2

About this gene

This gene has 2 transcripts (splice variants), 9 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000011096.8	nr6a1b-201	1501	455aa	ENSDARP00000019758.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q939	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,
ENSDART00000122773.3	nr6a1b-202	1317	422aa	ENSDARP00000109637.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QEH1	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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