TSC1 TSC complex subunit 1 Q92574 TSC1_HUMAN
Protein Coding Chr 9 9q34.13 Swiss-Prot reviewed Entrez 7248
Mutations
6,694
CL 592 · Tissue 5,936
Samples
544
CL 73 · Tissue 456
Peptides
486
unique mutant peptides
Transcripts
16
isoforms mutated

Stats by Source

Global, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Global = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Global can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

GlobalCell lineTissue
Mutations6,6945925,936
Samples54473456
Peptides48667423

Function

TSC1 · TSC complex subunit 1

This gene is a tumor suppressor gene that encodes the growth inhibitory protein hamartin. The encoded protein interacts with and stabilizes the GTPase activating protein tuberin. This hamartin-tuberin complex negatively regulates mammalian target of rapamycin complex 1 (mTORC1) signaling which is a major regulator of anabolic cell growth. This protein also functions as a co-chaperone for Hsp90 that inhibits its ATPase activity. This protein functions as a facilitator of Hsp90-mediated folding of kinase and non-kinase clients, including TSC2 and thereby preventing their ubiquitination and proteasomal degradation. Mutations in this gene have been associated with tuberous sclerosis and lymphangioleiomyomatosis. [provided by RefSeq, May 2022].

Isoforms & Proteins

16 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000298552 Q92574 581 424
ENST00000440111 Q92574 534 411
ENST00000642617 A0A2R8Y5S3* 534 411
ENST00000643875 Q92574 534 411
ENST00000644097 A0A2R8Y5S3* 534 411
ENST00000646625 Q92574 534 411
ENST00000642627 A0A2R8YFV7* 528 405
ENST00000643583 A0A2R8Y5N2* 528 405
ENST00000545250 Q92574-2 509 391
ENST00000643072 Q92574-2 509 391
ENST00000642646 A0A2R8YEI6* 242 176
ENST00000642745 A0A2R8YEI6* 242 176
ENST00000645150 A0A2R8YEI6* 242 176
ENST00000647462 A0A2R8Y6W1* 242 176
ENST00000647078 A0A2R8Y7E9* 203 149
ENST00000403810 Q86WV8* 198 144

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9q34.13
Entrez ID
Aliases
LAMTSC

Recurrent Mutations

Top recurrent amino-acid changes along the protein · needle height = number of mutations

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation Distribution

Where TSC1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TSC1 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 6,694 mutations in TSC1

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourcePeptide