ADSS2

Adenylosuccinate synthase 2 P30520 PURA2_HUMAN
Protein Coding Chr 1 1q44 Swiss-Prot reviewed Entrez 159
Mutations
37
CL 21 · Tissue 0
Samples
26
CL 20 · Tissue 0
Peptides
37
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
Mutations37210
Samples26200
Peptides37210

Function

ADSS2 · Adenylosuccinate synthase 2

This gene encodes the enzyme adenylosuccinate synthetase which catalyzes the first committed step in the conversion of inosine monophosphate to adenosine monophosphate. A pseudogene of this gene is found on chromosome 17.[provided by RefSeq, Nov 2010].

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
ENST00000366535 P30520 37 37

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q44
Entrez ID
Aliases
ADEHADSSADSS 2

Recurrent Mutations

All 37 amino-acid changes on canonical ENST00000366535 · 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 ADSS2 · 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 ADSS2 – 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
1/40 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Endometrial Carcinoma
2/42 5%
1/612 0%
Mesothelioma
1/62 2%
0/165 0%
Non-Cancerous
2/104 2%
0/830 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Other Solid Cancers
2/94 2%
0/1515 0%
Squamous Cell Lung Carcinoma
1/57 2%
0/810 0%
Melanoma
1/210 0%
1/1899 0%
Colorectal Carcinoma
3/143 2%
0/3239 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Pancreatic Carcinoma
1/89 1%
0/1611 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Glioma
1/52 2%
0/2127 0%
Gastric Carcinoma
1/74 1%
0/1809 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where ADSS2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ADSS2 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.

Mutations

All 37 mutations in ADSS2

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