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Gene : DHDDS Homo sapiens

Name  ? dehydrodolichyl diphosphate synthase subunit Cytological Location  1p36.11
Brief Description  dehydrodolichyl diphosphate synthase subunit
Description  The protein encoded by this gene catalyzes cis-prenyl chain elongation to produce the polyprenyl backbone of dolichol, a glycosyl carrier lipid required for the biosynthesis of several classes of glycoproteins. Mutations in this gene are associated with retinitis pigmentosa type 59. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]
  • synonyms:
  • HGNC:20603,
  • FLJ13102,
  • dehydrodolichyl diphosphate synthase,
  • DHDDS,
  • OTTHUMG00000003554,
  • CIT,
  • NM_024887,
  • HDS,
  • DEDSM,
  • CPT,
  • uc001bmk.4,
  • DS,
  • RP59,
  • hCIT,
  • DS,
  • HDS,
  • RP59,
  • AK023164,
  • hCIT
  • identifiers:
  • 79947,
  • ENSG00000117682,
  • DHDDS

Genome feature

Region: gene ? Length: 39025  
Location: 1:26432282-26471306 Cyto location: 1p36.11


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Proteins

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SNPs

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Disease

2 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

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Expression

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3753 SN Ps

5 Cross References

19 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results