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

Configure this page

Share this page

Bookmark this page

.

Gene: NOB1 ENSBTAG00000020633

.

Description

NIN1 (RPN12) binding [Source:VGNC Symbol;Acc:VGNC:32144]

Location

Primary_assembly 18: 36,812,458-36,829,147 reverse strand.

ARS-UCD2.0:CM008185.2

About this gene

This gene has 3 transcripts (splice variants) and 203 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000073783.2	NOB1-201	1769	455aa	ENSBTAP00000070112.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1NEN5	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000133183.1	NOB1-202	1910	429aa	ENSBTAP00000094802.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T7U2	-
ENSBTAT00000027497.3	NOB1-203	1741	413aa	ENSBTAP00000027497.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MDA9	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

.

Summary

.

.