Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- 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: Noc3l ENSRNOG00000013965

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Description

NOC3-like DNA replication regulator [Source:RGD Symbol;Acc:1560656]

Gene Synonyms

LOC361753, RGD1560656

Location

Primary_assembly 1: 245,969,179-245,997,708 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants) and 201 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000097060.2	Noc3l-202	3036	799aa	ENSRNOP00000089106.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AC09	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,
ENSRNOT00000019056.7	Noc3l-201	2936	799aa	ENSRNOP00000019056.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I192 D4AB23	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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