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: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Nopchap1 ENSRNOG00000008696

.

Description

NOP protein chaperone 1 [Source:RGD Symbol;Acc:1563365]

Gene Synonyms

LOC299700, RGD1563365

Location

Primary_assembly 7: 22,241,236-22,247,150 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants) and 102 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000011511.9	Nopchap1-201	1202	186aa	ENSRNOP00000011511.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IFG8 F1M6B3	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,
ENSRNOT00000119512.2	Nopchap1-202	1442	181aa	ENSRNOP00000079499.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZN53	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,

.

Strains

.

Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

.

Personal Data