SAT1 spermidine/spermine N1-acetyltransferase 1 [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: SAT1provided by VGNC
Official Full Name: spermidine/spermine N1-acetyltransferase 1provided by VGNC
Primary source: VGNC:VGNC:76973
See related: Ensembl:ENSMMUG00000060580
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Also known as: SAT
Orthologs: human mouse all
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Genomic context

Location:: chromosome: X

Exon count:: 6

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	X	NC_041774.1 (23581804..23584868)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	X	NC_027913.1 (23184163..23187231)

Chromosome X - NC_041774.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

SAT (e-PCR), detects polymorphism
- UniSTS:279057

RH77846 (e-PCR)
- UniSTS:78944

RH17558 (e-PCR)
- UniSTS:71014

RH81013 (e-PCR)
- UniSTS:86146

SAT1 (e-PCR)
- UniSTS:506529

MARC_4853-4854:991938661:1 (e-PCR)
- UniSTS:231098

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables N-acetyltransferase activity	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in cytosol	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: diamine acetyltransferase 1

NP_001244591.1

EC 2.3.1.57

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.