Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: noc3l ENSDARG00000002487

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Description

NOC3-like DNA replication regulator [Source:NCBI gene (formerly Entrezgene);Acc:321289]

Location

Chromosome 12: 5,399,680-5,418,340 reverse strand.

GRCz11:CM002896.2

About this gene

This gene has 3 transcripts (splice variants), 201 orthologues and is associated with 34 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000028043.9	noc3l-201	2569	800aa	ENSDARP00000004350.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6DRN3-1	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,
ENSDART00000152622.3	noc3l-203	2565	702aa	ENSDARP00000127021.1	Nonsense mediated decay	-	-
ENSDART00000123511.3	noc3l-202	603	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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