Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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  - Gene tree
  - Orthologues
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ID History
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Gene: NOB1 ENSBTAG00000020633

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Description

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

Location

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

ARS-UCD1.3:CM008185.2

About this gene

This gene has 3 transcripts (splice variants) and 200 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	F1MDA9	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,
ENSBTAT00000133183.1	NOB1-202	1910	429aa	ENSBTAP00000094802.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000027497.3	NOB1-203	1741	413aa	ENSBTAP00000027497.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MDA9	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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