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: NUDT9 ENSBTAG00000011354

.

Description

nudix hydrolase 9 [Source:VGNC Symbol;Acc:VGNC:32343]

Location

Primary_assembly 6: 102,292,170-102,365,731 forward strand.

ARS-UCD2.0:CM008173.2

About this gene

This gene has 5 transcripts (splice variants) and 209 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000015090.7	NUDT9-202	1295	350aa	ENSBTAP00000015090.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A7MBI8	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,
ENSBTAT00000109656.2	NUDT9-205	3165	324aa	ENSBTAP00000076145.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RV65	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,
ENSBTAT00000149663.1	NUDT9-203	3046	349aa	ENSBTAP00000107634.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000126619.2	NUDT9-204	2950	317aa	ENSBTAP00000076986.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RUR7	-
ENSBTAT00000095956.2	NUDT9-201	2861	329aa	ENSBTAP00000083675.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SLT6	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,

.

Summary

.

.