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Gene : SMS Homo sapiens

Name  ? spermine synthase Cytological Location  Xp22.11
Brief Description  spermine synthase
description  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]
  • synonyms:
  • SRS,
  • SpS,
  • SPMSY,
  • OTTHUMG00000021239,
  • SMS,
  • Snyder-Robinson X-linked mental retardation syndrome,
  • SpS,
  • uc004dag.5,
  • MRSR,
  • AD001528,
  • HGNC:11123,
  • MRSR,
  • SPMSY,
  • SRS,
  • NM_004595
  • identifiers:
  • 6611,
  • ENSG00000102172,
  • SMS

Genome feature

Region: gene ? Length: 54265  
Location: X:21940573-21994837 Cyto location: Xp22.11

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Gene --> GO terms.

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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



336 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

90 Rna Seq Results