AMY1C

Amylase alpha 1C P0DTE7 AMY1B_HUMAN
Protein Coding Chr 1 1p21.1 Swiss-Prot reviewed Entrez 278
Mutations
86
CL 22 · Tissue 64
Samples
82
CL 20 · Tissue 62
Peptides
63
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
Mutations862264
Samples822062
Peptides631949

Function

AMY1C · Amylase alpha 1C

Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, and thus catalyze the first step in digestion of dietary starch and glycogen. The human genome has a cluster of several amylase genes that are expressed at high levels in either salivary gland or pancreas. This gene encodes an amylase isoenzyme produced by the salivary gland. [provided by RefSeq, Jul 2008].

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
ENST00000370079 P0DTE7 86 63

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p21.1
Entrez ID
Aliases
AMY1

Recurrent Mutations

All 63 amino-acid changes on canonical ENST00000370079 · 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 AMY1C · 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 AMY1C – 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
1/42 2%
4/612 1%
Melanoma
2/210 1%
13/1899 1%
Squamous Cell Lung Carcinoma
1/57 2%
4/810 0%
Other Solid Cancers
1/94 1%
8/1515 1%
Non-Small Cell Lung Carcinoma
3/304 1%
3/1390 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Gastric Carcinoma
1/74 1%
3/1809 0%
Colorectal Carcinoma
3/143 2%
4/3239 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Other Blood Cancers
0/61 0%
4/2725 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
1/2550 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
2/2534 0%
Non-Cancerous
1/104 1%
0/830 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Glioma
0/52 0%
2/2127 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where AMY1C is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in AMY1C 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 1 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 86 mutations in AMY1C

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