TSC2 Gene

Alternative Names

  • TSC2
  • Tuberin
  • TSC4 Gene
  • TSC4

Associated Diseases

Tuberous Sclerosis 2
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OMIM Number

191092

NCBI Gene ID

7249

Uniprot ID

P49815

Length

41,556 bases

No. of Exons

44

No. of isoforms

8

Protein Name

Tuberin

Molecular Mass

200608 Da

Amino Acid Count

1807

Genomic Location

chr16:2,047,936-2,089,491

Gene Map Locus
16p13.3

Description

Mutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_000548.5:c.1754G>AUnited Arab EmiratesNC_000016.10:g.2070493G>ALikely Benign, Uncertain SignificanceUncertain SignificanceNG_005895.1:g.26188G>A; NM_000548.5:c.1754G>A; NP_000539.2:p.Arg585His39751506365084
NM_000548.5:c.1832G>ALebanonchr16:2070571PathogenicPathogenicTuberous Sclerosis 2NG_005895.1:g.26266G>A; NM_000548.5:c.1832G>A; NP_000539.2:p.Arg611Gln2893487212397
NM_000548.5:c.2834A>G Lebanonchr16:2076582BenignUncertain SignificanceBreast CancerNG_005895.1:g.32277A>G; NM_000548.5:c.2834A>G ; NP_000539.2:p.Lys945Arg886051791318323
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