Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Genetic Variation
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Gene: Nat9 ENSRNOG00000003264

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Description

N-acetyltransferase 9 [Source:RGD Symbol;Acc:1307096]

Gene Synonyms

LOC303669, RGD1307096

Location

Primary_assembly 10: 100,921,307-100,926,689 reverse strand.

GRCr8:CM070400.1

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
ENSRNOT00000004372.7	Nat9-201	1164	282aa	ENSRNOP00000004372.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FH79	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 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,
ENSRNOT00000100536.2	Nat9-202	1041	241aa	ENSRNOP00000082020.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZU60 A6HKK9	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,

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Summary

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