Also known as MRSR, SPMSY, SRS, SpS, spermine synthase, MRXSSR
protein-coding gene in the species Homo sapiens
Gene data
SMS- Name
- spermine synthase
- Type
- protein-coding
- Chromosome
- X
- Aliases
- MRSR, MRXSSR, SPMSY, SRS, SpS
This gene encodes a protein belonging to the spermidine/spermin synthase family and catalyzes the production of spermine from spermidine. Pseudogenes of this gene are located on chromosomes 1, 5, 6 and X. Mutations in this gene cause an X-linked intellectual disability called Snyder-Robinson Syndrome (SRS). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017].
via MyGene.info
Gene · Ensembl
spermine synthase
- Symbol
- SMS
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- Chr X:21,940,557-21,994,837
- Strand
- Forward (+)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Image
- Protein SMS PDB 3C6K.png
Show 5 more facts
- HomoloGene ID
- 88709
- exact match
- identifiers.org/ncbigene/6611
- genomic end
- 21994837
- genomic start
- 21940709
- cytogenetic location
- Xp22.11
Sources (8)
via Wikidata · CC0
Connections
Q180686
Entity
Ensembl genome database project
Entity
enzyme
Entity
Wikidata
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gene
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chromosome
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digital object identifier
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bibcode
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human genome
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Q229883
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base pair
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locus
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gene expression
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X chromosome
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Online Mendelian Inheritance in Man
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Protein Data Bank
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Q22908627
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Entrez
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Q905695
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Gene Ontology
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