3-Hydroxy-3-Methylglutaryl-CoA Synthase 2

Alternative Names

  • HMGCS2
  • 3-Hydroxy-3-Methylglutaryl-CoA Synthase, Mitochondrial
  • HMG-CoA Synthase, Mitochondrial
  • Mitochondrial HMG-CoA Synthase
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OMIM Number

600234

NCBI Gene ID

3158

Uniprot ID

P54868

Length

20,937 bases

No. of Exons

10

No. of isoforms

3

Protein Name

Hydroxymethylglutaryl-CoA synthase, mitochondrial

Molecular Mass

56635 Da

Amino Acid Count

508

Genomic Location

chr1:119,747,995-119,768,931

Gene Map Locus
1p12

Description

The protein encoded by this gene belongs to the HMG-CoA synthase family. It is a mitochondrial enzyme that catalyzes the first reaction of ketogenesis, a metabolic pathway that provides lipid-derived energy for various organs during times of carbohydrate deprivation, such as fasting. Mutations in this gene are associated with HMG-CoA synthase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_005518.4:c.1124C>TUnited Arab EmiratesNC_000001.11:g.119755490G>ABenign, Likely BenignBenignNG_013348.1:g.18443C>G; NM_005518.4:c.1124C>T; NP_005509.1:p.Ser375Phe151328418292332
NM_005518.4:c.754A>GUnited Arab EmiratesNC_000001.11:g.119759214T>CUncertain SignificanceNG_013348.1:g.14719A>G; NM_005518.4:c.754A>G; NP_005509.1:p.Ile252Val767113695
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