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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SATL1 ENSG00000184788

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Description

spermidine/spermine N1-acetyl transferase-like 1 [Source:HGNC Symbol;Acc:27992]

Location

Chromosome X: 84,347,293-84,364,054 reverse strand.

GRCh37:CM000685.1

About this gene

This gene has 3 transcripts (splice variants) and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000509231.1	SATL1-001	2224	632aa	ENSP00000425421.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS35343	E9PB72	-	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000395409.3	SATL1-202	2192	508aa	ENSP00000378804.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q86VE3	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000332921.5	SATL1-201	2151	445aa	ENSP00000329115.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q86VE3	NM_001012980.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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