SPAG11A

Sperm associated antigen 11A Q6PDA7-3 SG11A_HUMAN
Protein Coding Chr 8 8p23.1 Swiss-Prot reviewed Entrez 653423
Mutations
223
CL 76 · Tissue 147
Samples
80
CL 28 · Tissue 52
Peptides
84
unique mutant peptides
Transcripts
7
isoforms mutated

Stats by Source

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

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

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

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

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

TotalCell lineTissue
Mutations22376147
Samples802852
Peptides842962

Function

SPAG11A · Sperm associated antigen 11A

Involved in antimicrobial humoral immune response mediated by antimicrobial peptide and cytolysis by host of symbiont cells. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

7 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
ENST00000642566 A0A2R8Y853* 48 33
ENST00000326558 A0A0A0MR37* 44 30
ENST00000326625 C9IZU7* 41 28
ENST00000434307 J3KR45* 37 17
ENST00000454911 C9JP82* 30 12
ENST00000351436 Q6PDA7-3 16 13
ENST00000400125 Q08648-3 7 5

Gene Properties

Type
Protein Coding
Chromosome
8
Cytoband
8p23.1
Entrez ID
Aliases
EDDM2AHE2

Recurrent Mutations

All 13 amino-acid changes on canonical ENST00000351436 · needle height = samples · drag the mini-map to zoom

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 frequency across cancer types

% of samples with a missense/complex mutation in SPAG11A · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in SPAG11A – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Squamous Cell Lung Carcinoma
5/57 9%
5/810 1%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Non-Small Cell Lung Carcinoma
11/304 4%
5/1390 0%
Medulloblastoma
0/0 0%
2/450 0%
Mesothelioma
1/62 2%
0/165 0%
Colorectal Carcinoma
3/143 2%
8/3239 0%
Endometrial Carcinoma
0/42 0%
2/612 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Melanoma
2/210 1%
4/1899 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Small Cell Lung Carcinoma
2/9 22%
0/752 0%
Other Sarcomas
1/69 1%
1/699 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Solid Cancers
0/94 0%
2/1515 0%
Other Blood Cancers
0/61 0%
3/2725 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Neuroblastoma
1/87 1%
0/1331 0%
Gastric Carcinoma
0/74 0%
1/1809 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where SPAG11A is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in SPAG11A 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.

Mutations

All 223 mutations in SPAG11A

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 CDSTypeSourceMutant PeptideWild-type Peptide