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

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Gene: Nccrp1 ENSRNOG00000054506

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Description

NCCRP1, F-box associated domain containing [Source:RGD Symbol;Acc:1305932]

Gene Synonyms

LOC292755, RGD1305932

Location

Primary_assembly 1: 92,962,618-92,966,410 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant), 165 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000092044.4	Nccrp1-201	1617	291aa	ENSRNOP00000070205.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J9J7 D3ZQ18	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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