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: nlrb5 ENSDARG00000090699

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Description

NOD-like receptor family B, member 5 [Source:ZFIN;Acc:ZDB-GENE-081015-5]

Gene Synonyms

NLR-B5, NLR-B6, nalpl1, nlrp6(3of5)

Location

Chromosome 2: 43,851,983-43,871,387 forward strand.

GRCz11:CM002886.2

About this gene

This gene has 2 transcripts (splice variants), 183 orthologues and 372 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000126413.3	nlrb5-201	2318	651aa	ENSDARP00000107209.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F5K1	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,
ENSDART00000151951.2	nlrb5-202	1580	526aa	ENSDARP00000126537.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	K7DYK8	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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