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

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Gene: npffr1l1 ENSDARG00000054203

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Description

neuropeptide FF receptor 1 like 1 [Source:ZFIN;Acc:ZDB-GENE-091118-18]

Gene Synonyms

gnihr1, si:dkey-261l11.2

Location

Chromosome 10: 40,951,697-40,968,095 reverse strand.

GRCz11:CM002894.2

About this gene

This gene has 2 transcripts (splice variants), 30 orthologues and 29 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000076359.5	npffr1l1-201	1297	398aa	ENSDARP00000070833.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D2Y177	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,
ENSDART00000184104.1	npffr1l1-202	3195	398aa	ENSDARP00000144867.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D2Y177	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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