GUCD1

Guanylyl cyclase domain containing 1 Q96NT3 GUCD1_HUMAN
Protein Coding Chr 22 22q11.23 Swiss-Prot reviewed Entrez 83606
Mutations
459
CL 55 · Tissue 399
Samples
111
CL 21 · Tissue 86
Peptides
110
unique mutant peptides
Transcripts
6
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
Mutations45955399
Samples1112186
Peptides1101988

Isoforms & Proteins

6 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
ENST00000621833 A0A087WVD9* 101 81
ENST00000404664 Q96NT3-3 97 78
ENST00000435822 Q96NT3-2 92 70
ENST00000407471 Q96NT3 84 69
ENST00000402766 E9PGZ7* 43 35
ENST00000447813 E7EX77* 42 34

Gene Properties

Type
Protein Coding
Chromosome
22
Cytoband
22q11.23
Entrez ID
Aliases
C22orf13LLN4

Recurrent Mutations

All 78 amino-acid changes on canonical ENST00000404664 · 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 GUCD1 · 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 GUCD1 – 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
6/40 15%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
1/42 2%
8/612 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Colorectal Carcinoma
4/143 3%
12/3239 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Melanoma
0/210 0%
7/1899 0%
Other Solid Cancers
2/94 2%
3/1515 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Non-Small Cell Lung Carcinoma
0/304 0%
5/1390 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Medulloblastoma
0/0 0%
1/450 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Non-Cancerous
0/104 0%
2/830 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%
Other Blood Cancers
0/61 0%
5/2725 0%
Glioma
0/52 0%
3/2127 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Sarcomas
0/69 0%
1/699 0%
B-Lymphoblastic Leukemia
2/55 4%
1/2640 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Breast Carcinoma
0/144 0%
3/3264 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

Where GUCD1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GUCD1 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 459 mutations in GUCD1

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