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: nlrc3 ENSDARG00000103146

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Description

NLR family, CARD domain containing 3 [Source:ZFIN;Acc:ZDB-GENE-071119-1]

Gene Synonyms

NLR-A3, nod3

Location

Chromosome 24: 37,449,893-37,466,754 forward strand.

GRCz11:CM002908.2

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 372 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000164405.2	nlrc3-201	2224	741aa	ENSDARP00000140992.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IZ79	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000165775.2	nlrc3-202	521	174aa	ENSDARP00000131180.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IDV8	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, 5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,

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Summary

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