HYKK

Hydroxylysine kinase A2RU49 HYKK_HUMAN
Protein Coding Chr 15 15q25.1 Swiss-Prot reviewed Entrez 123688
Mutations
489
CL 58 · Tissue 424
Samples
136
CL 21 · Tissue 113
Peptides
117
unique mutant peptides
Transcripts
5
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
Mutations48958424
Samples13621113
Peptides11717101

Function

HYKK · Hydroxylysine kinase

Enables hydroxylysine kinase activity. Predicted to be involved in lysine catabolic process. Predicted to be located in mitochondrial matrix. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

5 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
ENST00000388988 A2RU49 141 114
ENST00000569878 A2RU49 131 110
ENST00000566332 A0A0C4DGM4* 73 65
ENST00000408962 A2RU49-3 72 64
ENST00000563233 A2RU49-3 72 64

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q25.1
Entrez ID
Aliases
AGPHD1

Recurrent Mutations

All 114 amino-acid changes on canonical ENST00000388988 · 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 HYKK · 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 HYKK – 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
Rhabdomyosarcoma
0/33 0%
3/171 2%
Endometrial Carcinoma
0/42 0%
8/612 1%
Melanoma
4/210 2%
16/1899 1%
Plasma Cell Myeloma
1/44 2%
2/305 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Cervical Carcinoma
2/35 6%
1/422 0%
Colorectal Carcinoma
5/143 4%
17/3239 1%
Bladder Carcinoma
0/58 0%
6/956 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Medulloblastoma
0/0 0%
2/450 0%
Glioma
1/52 2%
6/2127 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Other Sarcomas
0/69 0%
2/699 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Non-Small Cell Lung Carcinoma
3/304 1%
1/1390 0%
Thyroid Gland Carcinoma
1/45 2%
3/1592 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Kidney Carcinoma
1/85 1%
2/1862 0%
B-Lymphoblastic Leukemia
2/55 4%
1/2640 0%
Non-Cancerous
0/104 0%
1/830 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Neuroblastoma
0/87 0%
1/1331 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in HYKK 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 489 mutations in HYKK

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