KIAA0100

Uncharacterized protein Q14667 BLTP2_HUMAN
Swiss-Prot reviewed
Mutations
1,705
CL 144 · Tissue 1,543
Samples
755
CL 69 · Tissue 677
Peptides
723
unique mutant peptides
Transcripts
2
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
Mutations1,7051441,543
Samples75569677
Peptides72373657

Isoforms & Proteins

2 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
ENST00000528896 Q14667 905 714
ENST00000389003 K7EQ86* 800 636

Gene Properties

Recurrent Mutations

All 714 amino-acid changes on canonical ENST00000528896 · 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 KIAA0100 · 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 KIAA0100 – 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
3/40 8%
0/0 0%
Endometrial Carcinoma
3/42 7%
45/612 7%
Melanoma
4/210 2%
82/1899 4%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Colorectal Carcinoma
11/143 8%
101/3239 3%
Bladder Carcinoma
0/58 0%
32/956 3%
Burkitts Lymphoma
1/32 3%
6/196 3%
Hodgkins Lymphoma
0/16 0%
4/122 3%
Non-Small Cell Lung Carcinoma
7/304 2%
42/1390 3%
Other Solid Cancers
3/94 3%
42/1515 3%
Gastric Carcinoma
2/74 3%
47/1809 3%
Squamous Cell Lung Carcinoma
3/57 5%
16/810 2%
Glioblastoma
2/98 2%
0/0 0%
Cervical Carcinoma
1/35 3%
8/422 2%
Germ Cell Tumour
0/25 0%
3/169 2%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Head and Neck Carcinoma
0/85 0%
22/1574 1%
Other Sarcomas
2/69 3%
8/699 1%
Ovarian Carcinoma
0/109 0%
13/998 1%
Hepatocellular Carcinoma
0/46 0%
26/2210 1%
Esophageal Carcinoma
2/23 9%
7/769 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
27/2550 1%
Biliary Tract Carcinoma
1/54 2%
10/950 1%
Kidney Carcinoma
0/85 0%
20/1862 1%
Glioma
0/52 0%
22/2127 1%
Breast Carcinoma
4/144 3%
29/3264 1%
Neuroendocrine Tumour
3/154 2%
4/577 1%
Osteosarcoma
1/45 2%
1/166 1%

Mutation Distribution

Where KIAA0100 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KIAA0100 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 1,705 mutations in KIAA0100

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