UBALD1

UBA like domain containing 1 Q8TB05 UBAD1_HUMAN
Protein Coding Chr 16 16p13.3 Swiss-Prot reviewed Entrez 124402
Mutations
482
CL 52 · Tissue 395
Samples
124
CL 32 · Tissue 90
Peptides
107
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
Mutations48252395
Samples1243290
Peptides1072281

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
ENST00000283474 Q8TB05 123 69
ENST00000590891 Q8TB05-2 93 56
ENST00000591401 K7EQ49* 93 57
ENST00000591897 D3DUE0* 86 51
ENST00000587615 K7EM88* 64 48
ENST00000590965 K7EM52* 12 10
ENST00000587649 K7EKR5* 11 9

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p13.3
Entrez ID
Aliases
FAM100APP11303

Recurrent Mutations

All 69 amino-acid changes on canonical ENST00000283474 · 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 UBALD1 · 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 UBALD1 – 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
Oral Cavity Carcinoma
2/54 4%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Glioblastoma
2/98 2%
0/0 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
25/2550 1%
Mesothelioma
2/62 3%
0/165 0%
Thyroid Gland Carcinoma
0/45 0%
14/1592 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Bladder Carcinoma
4/58 7%
2/956 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Gastric Carcinoma
0/74 0%
8/1809 0%
Colorectal Carcinoma
3/143 2%
10/3239 0%
Ovarian Carcinoma
1/109 1%
3/998 0%
Other Solid Cancers
2/94 2%
3/1515 0%
Endometrial Carcinoma
1/42 2%
1/612 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Medulloblastoma
0/0 0%
1/450 0%
Non-Cancerous
2/104 2%
0/830 0%
Melanoma
2/210 1%
2/1899 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Non-Small Cell Lung Carcinoma
0/304 0%
3/1390 0%
Pancreatic Carcinoma
2/89 2%
1/1611 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Squamous Cell Lung Carcinoma
1/57 2%
0/810 0%
Kidney Carcinoma
2/85 2%
0/1862 0%
Prostate Carcinoma
0/13 0%
2/2105 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Glioma
0/52 0%
2/2127 0%
Breast Carcinoma
1/144 1%
2/3264 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%

Mutation Distribution

Where UBALD1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in UBALD1 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 482 mutations in UBALD1

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