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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Phenotypes
Genetic Variation
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Gene: Nadsyn1 ENSRNOG00000020736

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Description

NAD synthetase 1 [Source:RGD Symbol;Acc:727801]

Location

Primary_assembly 1: 208,410,914-208,439,207 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 211 orthologues and is associated with 9 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000107505.2	Nadsyn1-202	2711	738aa	ENSRNOP00000085928.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GEG1	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,
ENSRNOT00000103972.2	Nadsyn1-201	2712	737aa	ENSRNOP00000080154.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZP01	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,

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Strains

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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.

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Personal Data