GAD1

Glutamate decarboxylase 1 Q99259 DCE1_HUMAN
Protein Coding Chr 2 2q31.1 Swiss-Prot reviewed Entrez 2571
Mutations
959
CL 102 · Tissue 842
Samples
386
CL 63 · Tissue 317
Peptides
299
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
Mutations959102842
Samples38663317
Peptides29947259

Function

GAD1 · Glutamate decarboxylase 1

This gene encodes one of several forms of glutamic acid decarboxylase, identified as a major autoantigen in insulin-dependent diabetes. The enzyme encoded is responsible for catalyzing the production of gamma-aminobutyric acid from L-glutamic acid. A pathogenic role for this enzyme has been identified in the human pancreas since it has been identified as an autoantigen and an autoreactive T cell target in insulin-dependent diabetes. This gene may also play a role in the stiff man syndrome. Deficiency in this enzyme has been shown to lead to pyridoxine dependency with seizures. Alternative splicing of this gene results in two products, the predominant 67-kD form and a less-frequent 25-kD form. [provided by RefSeq, Jul 2008].

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
ENST00000358196 Q99259 385 267
ENST00000625689 Q99259-4 266 191
ENST00000344257 Q99259-3 154 105
ENST00000375272 Q99259-3 154 105

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q31.1
Entrez ID
Aliases
CPSQ1DEE89GADGAD-67SCP

Recurrent Mutations

All 267 amino-acid changes on canonical ENST00000358196 · 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 GAD1 · 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 GAD1 – 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
Chordoma
0/7 0%
1/13 8%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Melanoma
8/210 4%
56/1899 3%
Endometrial Carcinoma
4/42 10%
9/612 1%
Colorectal Carcinoma
8/143 6%
48/3239 1%
Non-Small Cell Lung Carcinoma
14/304 5%
13/1390 1%
Cervical Carcinoma
1/35 3%
6/422 1%
Squamous Cell Lung Carcinoma
2/57 4%
11/810 1%
Bladder Carcinoma
2/58 3%
13/956 1%
Other Solid Cancers
0/94 0%
19/1515 1%
Gastric Carcinoma
0/74 0%
22/1809 1%
Chondrosarcoma
1/14 7%
0/75 0%
Small Cell Lung Carcinoma
0/9 0%
8/752 1%
Thyroid Gland Carcinoma
1/45 2%
13/1592 1%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Neuroendocrine Tumour
2/154 1%
4/577 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Ovarian Carcinoma
4/109 4%
4/998 0%
Hepatocellular Carcinoma
1/46 2%
15/2210 1%
Esophageal Carcinoma
0/23 0%
5/769 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Non-Cancerous
0/104 0%
5/830 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Glioma
0/52 0%
11/2127 1%
Osteosarcoma
1/45 2%
0/166 0%
Mesothelioma
1/62 2%
0/165 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
10/2550 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Pancreatic Carcinoma
0/89 0%
6/1611 0%

Mutation Distribution

Where GAD1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GAD1 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 959 mutations in GAD1

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