NME6

NME/NM23 nucleoside diphosphate kinase 6 O75414 NDK6_HUMAN
Protein Coding Chr 3 3p21.31 Swiss-Prot reviewed Entrez 10201
Mutations
808
CL 138 · Tissue 668
Samples
94
CL 18 · Tissue 74
Peptides
119
unique mutant peptides
Transcripts
13
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
Mutations808138668
Samples941874
Peptides1192199

Function

NME6 · NME/NM23 nucleoside diphosphate kinase 6

Nucleoside diphosphate (NDP) kinases (EC 2.7.4.6), such as NME6, are ubiquitous enzymes that catalyze transfer of gamma-phosphates, via a phosphohistidine intermediate, between nucleoside and dioxynucleoside tri- and diphosphates (Mehus et al., 1999 [PubMed 10453732]).[supplied by OMIM, Jul 2010].

Isoforms & Proteins

13 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
ENST00000442597 O75414 84 59
ENST00000421967 O75414-4 76 58
ENST00000415053 O75414 75 57
ENST00000426689 O75414 75 57
ENST00000452211 O75414 75 57
ENST00000643457 O75414 75 57
ENST00000447314 C9JQB1* 60 44
ENST00000435684 O75414-3 58 48
ENST00000451657 O75414-3 58 48
ENST00000643011 A0A2R8Y7V2* 50 34
ENST00000415644 O75414-2 46 36
ENST00000444069 A0A2R8Y547* 38 25
ENST00000642710 A0A2R8Y547* 38 25

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p21.31
Entrez ID
Aliases
IPIA-ALPHANDK 6NDK6NM23-H6

Recurrent Mutations

All 59 amino-acid changes on canonical ENST00000442597 · 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 NME6 · 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 NME6 – 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
2/40 5%
0/0 0%
Endometrial Carcinoma
4/42 10%
4/612 1%
Chondrosarcoma
1/14 7%
0/75 0%
Mesothelioma
2/62 3%
0/165 0%
Melanoma
2/210 1%
15/1899 1%
Gastric Carcinoma
0/74 0%
10/1809 1%
Osteosarcoma
0/45 0%
1/166 1%
Non-Small Cell Lung Carcinoma
4/304 1%
3/1390 0%
Squamous Cell Lung Carcinoma
1/57 2%
2/810 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
8/2550 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Colorectal Carcinoma
0/143 0%
9/3239 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Wilms Tumour
0/5 0%
1/474 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Breast Carcinoma
0/144 0%
4/3264 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Glioma
0/52 0%
2/2127 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Neuroblastoma
1/87 1%
0/1331 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

Where NME6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in NME6 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 808 mutations in NME6

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