ANKIB1

Ankyrin repeat and IBR domain containing 1 Q9P2G1 AKIB1_HUMAN
Protein Coding Chr 7 7q21.2 Swiss-Prot reviewed Entrez 54467
Mutations
609
CL 117 · Tissue 488
Samples
568
CL 105 · Tissue 459
Peptides
391
unique mutant peptides
Transcripts
1
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
Mutations609117488
Samples568105459
Peptides39173326

Function

ANKIB1 · Ankyrin repeat and IBR domain containing 1

Predicted to enable ubiquitin conjugating enzyme binding activity and ubiquitin protein ligase activity. Predicted to be involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process; protein polyubiquitination; and ubiquitin-dependent protein catabolic process. Predicted to be part of ubiquitin ligase complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

1 transcript · 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
ENST00000265742 Q9P2G1 609 391

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7q21.2
Entrez ID

Recurrent Mutations

All 391 amino-acid changes on canonical ENST00000265742 · 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 ANKIB1 · 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 ANKIB1 – 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
8/40 20%
0/0 0%
Endometrial Carcinoma
4/42 10%
32/612 5%
Hodgkins Lymphoma
6/16 38%
0/122 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
81/2550 3%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Non-Small Cell Lung Carcinoma
13/304 4%
35/1390 3%
Melanoma
7/210 3%
47/1899 2%
Mesothelioma
4/62 6%
1/165 1%
Burkitts Lymphoma
3/32 9%
2/196 1%
Other Solid Cancers
2/94 2%
33/1515 2%
Squamous Cell Lung Carcinoma
5/57 9%
13/810 2%
Small Cell Lung Carcinoma
0/9 0%
14/752 2%
Bladder Carcinoma
1/58 2%
17/956 2%
Colorectal Carcinoma
9/143 6%
47/3239 1%
Gastric Carcinoma
4/74 5%
25/1809 1%
Osteosarcoma
3/45 7%
0/166 0%
Meningioma
2/3 67%
1/252 0%
Neuroendocrine Tumour
6/154 4%
1/577 0%
Cervical Carcinoma
0/35 0%
4/422 1%
Esophageal Carcinoma
0/23 0%
7/769 1%
Hepatocellular Carcinoma
0/46 0%
18/2210 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Biliary Tract Carcinoma
0/54 0%
6/950 1%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Non-Cancerous
0/104 0%
5/830 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Breast Carcinoma
6/144 4%
11/3264 0%

Mutation Distribution

Where ANKIB1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ANKIB1 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 609 mutations in ANKIB1

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