PANK1

Pantothenate kinase 1 Q8TE04-2 PANK1_HUMAN
Protein Coding Chr 10 10q23.31 Swiss-Prot reviewed Entrez 53354
Mutations
289
CL 48 · Tissue 236
Samples
171
CL 37 · Tissue 130
Peptides
145
unique mutant peptides
Transcripts
3
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
Mutations28948236
Samples17137130
Peptides14530119

Function

PANK1 · Pantothenate kinase 1

This gene encodes a member of the pantothenate kinase family. Pantothenate kinases are key regulatory enzymes in the biosynthesis of coenzyme A (CoA). The encoded protein catalyzes the first and rate-limiting enzymatic reaction in CoA biosynthesis and is regulated by CoA through feedback inhibition. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. This gene and an intronic miRNA on the same strand are co-regulated by the tumor suppressor p53 (see PMID 20833636). [provided by RefSeq, Apr 2011].

Isoforms & Proteins

3 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
ENST00000342512 Q8TE04-2 136 112
ENST00000322191 Q8TE04-3 106 88
ENST00000307534 A0A8C8KBT8* 47 36

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q23.31
Entrez ID
Aliases
PANK

Recurrent Mutations

All 115 amino-acid changes on canonical ENST00000342512 · 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 PANK1 · 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 PANK1 – 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
Endometrial Carcinoma
3/42 7%
7/612 1%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Melanoma
2/210 1%
23/1899 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Colorectal Carcinoma
10/143 7%
18/3239 1%
Bladder Carcinoma
0/58 0%
8/956 1%
Gastric Carcinoma
1/74 1%
12/1809 1%
Neuroendocrine Tumour
4/154 3%
0/577 0%
Other Solid Cancers
3/94 3%
5/1515 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Kidney Carcinoma
0/85 0%
6/1862 0%
Non-Small Cell Lung Carcinoma
2/304 1%
3/1390 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Ovarian Carcinoma
2/109 2%
1/998 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Breast Carcinoma
0/144 0%
8/3264 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
5/2550 0%
Glioma
0/52 0%
5/2127 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
3/2534 0%
Prostate Carcinoma
0/13 0%
4/2105 0%
Head and Neck Carcinoma
1/85 1%
2/1574 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Other Sarcomas
0/69 0%
1/699 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
B-Lymphoblastic Leukemia
1/55 2%
2/2640 0%
Non-Cancerous
0/104 0%
1/830 0%
Neuroblastoma
1/87 1%
0/1331 0%

Mutation Distribution

Where PANK1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PANK1 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 289 mutations in PANK1

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