AGTPBP1

ATP/GTP binding carboxypeptidase 1 Q9UPW5 CBPC1_HUMAN
Protein Coding Chr 9 9q21.33 Swiss-Prot reviewed Entrez 23287
Mutations
1,895
CL 250 · Tissue 1,618
Samples
484
CL 98 · Tissue 377
Peptides
413
unique mutant peptides
Transcripts
4
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
Mutations1,8952501,618
Samples48498377
Peptides41366339

Function

AGTPBP1 · ATP/GTP binding carboxypeptidase 1

NNA1 is a zinc carboxypeptidase that contains nuclear localization signals and an ATP/GTP-binding motif that was initially cloned from regenerating spinal cord neurons of the mouse.[supplied by OMIM, Jul 2002].

Isoforms & Proteins

4 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
ENST00000357081 Q9UPW5 527 395
ENST00000337006 J3KNS1* 459 367
ENST00000628899 Q9UPW5-3 455 363
ENST00000376083 Q9UPW5-2 454 362

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9q21.33
Entrez ID
Aliases
CCP1CONDCANNA1

Recurrent Mutations

All 395 amino-acid changes on canonical ENST00000357081 · 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 AGTPBP1 · 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 AGTPBP1 – 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%
Oral Cavity Carcinoma
4/54 7%
0/0 0%
Endometrial Carcinoma
7/42 17%
26/612 4%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
Squamous Cell Lung Carcinoma
2/57 4%
18/810 2%
Melanoma
7/210 3%
40/1899 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Colorectal Carcinoma
14/143 10%
59/3239 2%
Neuroendocrine Tumour
10/154 6%
4/577 1%
Gastric Carcinoma
2/74 3%
28/1809 2%
Cervical Carcinoma
1/35 3%
5/422 1%
Non-Small Cell Lung Carcinoma
7/304 2%
15/1390 1%
Bladder Carcinoma
0/58 0%
12/956 1%
Hepatocellular Carcinoma
2/46 4%
24/2210 1%
Chondrosarcoma
1/14 7%
0/75 0%
Ovarian Carcinoma
2/109 2%
10/998 1%
Head and Neck Carcinoma
2/85 2%
16/1574 1%
Glioblastoma
1/98 1%
0/0 0%
Ewings Sarcoma
3/63 5%
0/262 0%
Mesothelioma
2/62 3%
0/165 0%
Burkitts Lymphoma
2/32 6%
0/196 0%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Other Solid Cancers
0/94 0%
13/1515 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
19/2550 1%
Biliary Tract Carcinoma
0/54 0%
8/950 1%
Non-Cancerous
2/104 2%
5/830 1%
Thyroid Gland Carcinoma
2/45 4%
10/1592 1%
Breast Carcinoma
7/144 5%
16/3264 0%
Glioma
0/52 0%
13/2127 1%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%

Mutation Distribution

Where AGTPBP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in AGTPBP1 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 1,895 mutations in AGTPBP1

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