STRADA STE20 related adaptor alpha Q7RTN6 STRAA_HUMAN
Protein Coding Chr 17 17q23.3 Swiss-Prot reviewed Entrez 92335
Mutations
2,624
CL 334 · Tissue 2,265
Samples
173
CL 32 · Tissue 139
Peptides
195
unique mutant peptides
Transcripts
23
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
Mutations2,6243342,265
Samples17332139
Peptides19532167

Function

STRADA · STE20 related adaptor alpha

The protein encoded by this gene contains a STE20-like kinase domain, but lacks several residues that are critical for catalytic activity, so it is termed a 'pseudokinase'. The protein forms a heterotrimeric complex with serine/threonine kinase 11 (STK11, also known as LKB1) and the scaffolding protein calcium binding protein 39 (CAB39, also known as MO25). The protein activates STK11 leading to the phosphorylation of both proteins and excluding STK11 from the nucleus. The protein is necessary for STK11-induced G1 cell cycle arrest. A mutation in this gene has been shown to result in polyhydramnios, megalencephaly, and symptomatic epilepsy (PMSE) syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described but their full-length nature is not known. [provided by RefSeq, Sep 2009].

Isoforms & Proteins

23 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
ENST00000336174 Q7RTN6 165 124
ENST00000638193 A0A1W2PQF1* 145 118
ENST00000638708 A0A1W2PPJ9* 141 114
ENST00000639835 Q7RTN6-3 141 114
ENST00000640999 Q7RTN6-3 141 114
ENST00000375840 Q7RTN6-5 134 109
ENST00000638702 Q7RTN6-5 134 109
ENST00000392950 Q7RTN6-2 132 109
ENST00000640979 A0A1W2PPM8* 130 106
ENST00000638888 A0A1W2PPG2* 124 101
ENST00000582137 Q7RTN6-6 116 94
ENST00000640086 A0A1W2PR00* 116 94
ENST00000447001 Q7RTN6-4 112 91
ENST00000638698 A0A1W2PNV7* 111 88
ENST00000640679 A0A1W2PNV7* 111 88
ENST00000638276 A0A1W2PQE8* 109 89
ENST00000638309 A0A1W2PS04* 99 80
ENST00000578008 J3QS66* 91 73
ENST00000245865 A0ACM8PXG4* 84 68
ENST00000617949 A0ACM8PXG4* 84 68
ENST00000640397 A0A1W2PRQ6* 81 65
ENST00000578801 J3QQS3* 69 57
ENST00000579340 J3KSK5* 54 45

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q23.3
Entrez ID
Aliases
LYK5NY-BR-96PMSESTLK5STRADSTRAD alpha

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

Mutation counts by tissue
Mutation Distribution

How many mutations in STRADA 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 2,624 mutations in STRADA

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