AIG1

Androgen induced 1 Q9NVV5 AIG1_HUMAN
Protein Coding Chr 6 6q24.2 Swiss-Prot reviewed Entrez 51390
Mutations
368
CL 71 · Tissue 296
Samples
100
CL 33 · Tissue 66
Peptides
93
unique mutant peptides
Transcripts
6
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
Mutations36871296
Samples1003366
Peptides932571

Function

AIG1 · Androgen induced 1

Enables hydrolase activity. Involved in long-chain fatty acid catabolic process. Located in membrane. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

6 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
ENST00000357847 Q9NVV5 95 72
ENST00000275235 Q9NVV5-1 85 72
ENST00000646199 A0A2R8YCJ8* 79 66
ENST00000494282 Q9NVV5-5 43 37
ENST00000629020 Q9NVV5-6 43 37
ENST00000367596 Q5THU2* 23 17

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6q24.2
Entrez ID
Aliases
AIG-1dJ95L4.1

Recurrent Mutations

All 72 amino-acid changes on canonical ENST00000357847 · 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 AIG1 · 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 AIG1 – 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
2/40 5%
0/0 0%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Endometrial Carcinoma
1/42 2%
8/612 1%
Neuroendocrine Tumour
5/154 3%
0/577 0%
Melanoma
5/210 2%
8/1899 0%
Non-Small Cell Lung Carcinoma
4/304 1%
6/1390 0%
Colorectal Carcinoma
4/143 3%
9/3239 0%
Esophageal Carcinoma
3/23 13%
0/769 0%
Gastric Carcinoma
1/74 1%
6/1809 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Other Solid Cancers
2/94 2%
2/1515 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Other Sarcomas
0/69 0%
1/699 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
2/2534 0%
Non-Cancerous
0/104 0%
1/830 0%
Glioma
0/52 0%
2/2127 0%
Prostate Carcinoma
1/13 8%
1/2105 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%

Mutation Distribution

Where AIG1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in AIG1 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 368 mutations in AIG1

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