GALNT4

Polypeptide N-acetylgalactosaminyltransferase 4 Q8N4A0 GALT4_HUMAN
Protein Coding Chr 12 12q21.33 Swiss-Prot reviewed Entrez 8693
Mutations
218
CL 32 · Tissue 182
Samples
202
CL 32 · Tissue 167
Peptides
162
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
Mutations21832182
Samples20232167
Peptides16221141

Function

GALNT4 · Polypeptide N-acetylgalactosaminyltransferase 4

This gene encodes a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-T) family of enzymes. GalNAc-Ts initiate mucin-type O-linked glycosylation in the Golgi apparatus by catalyzing the transfer of GalNAc to serine and threonine residues on target proteins. They are characterized by an N-terminal transmembrane domain, a stem region, a lumenal catalytic domain containing a GT1 motif and Gal/GalNAc transferase motif, and a C-terminal ricin/lectin-like domain. GalNAc-Ts have different, but overlapping, substrate specificities and patterns of expression. In vitro, the encoded protein can complement other GalNAc-Ts in the complete O-glycosylation of the mucin-1 tandem repeat and can O-glycosylate the P-selectin glycoprotein ligand-1 molecule. The coding region of this gene is contained within a single exon. Fusion transcripts, which combine part of this gene with the 5' exons of the neighboring POC1B (POC1 centriolar protein homolog B) gene, also exist. [provided by RefSeq, Dec 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
ENST00000529983 Q8N4A0 218 162

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q21.33
Entrez ID
Aliases
GALNAC-T4GALNACT4

Recurrent Mutations

All 162 amino-acid changes on canonical ENST00000529983 · 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 GALNT4 · 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 GALNT4 – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
4/42 10%
15/612 2%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Melanoma
2/210 1%
23/1899 1%
Glioblastoma
1/98 1%
0/0 0%
Bladder Carcinoma
2/58 3%
8/956 1%
Non-Small Cell Lung Carcinoma
6/304 2%
10/1390 1%
Gastric Carcinoma
2/74 3%
12/1809 1%
Other Solid Cancers
1/94 1%
10/1515 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Colorectal Carcinoma
2/143 1%
19/3239 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Hepatocellular Carcinoma
0/46 0%
11/2210 0%
Squamous Cell Lung Carcinoma
1/57 2%
3/810 0%
Mesothelioma
1/62 2%
0/165 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Glioma
2/52 4%
6/2127 0%
Ovarian Carcinoma
0/109 0%
4/998 0%
Neuroblastoma
1/87 1%
4/1331 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Prostate Carcinoma
1/13 8%
5/2105 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
6/2550 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Medulloblastoma
0/0 0%
1/450 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Breast Carcinoma
0/144 0%
5/3264 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Other Sarcomas
0/69 0%
1/699 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Pancreatic Carcinoma
1/89 1%
1/1611 0%

Mutation Distribution

Where GALNT4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GALNT4 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 218 mutations in GALNT4

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