DNAH10

Dynein axonemal heavy chain 10 Q8IVF4 DYH10_HUMAN
Protein Coding Chr 12 12q24.31 Swiss-Prot reviewed Entrez 196385
Mutations
5,772
CL 864 · Tissue 4,856
Samples
2,026
CL 386 · Tissue 1,617
Peptides
1,892
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
Mutations5,7728644,856
Samples2,0263861,617
Peptides1,8923461,607

Function

DNAH10 · Dynein axonemal heavy chain 10

Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH10 is an inner arm dynein heavy chain (Maiti et al., 2000 [PubMed 11175280]).[supplied by OMIM, Mar 2008].

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
ENST00000409039 A0A1C7CYW8* 2,480 1,772
ENST00000638045 Q8IVF4 2,474 1,767
ENST00000614082 - 556 391
ENST00000673944 A0A669KB38* 259 239
ENST00000631855 A0A0J9YY17* 3 3

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q24.31
Entrez ID
Aliases
SPGF56

Recurrent Mutations

All 1767 amino-acid changes on canonical ENST00000638045 · 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 DNAH10 · 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 DNAH10 – 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
16/40 40%
0/0 0%
Chronic Myelogenous Leukemia
5/25 20%
0/0 0%
Oral Cavity Carcinoma
10/54 19%
0/0 0%
Melanoma
37/210 18%
324/1899 17%
Endometrial Carcinoma
20/42 48%
89/612 15%
Glioblastoma
16/98 16%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
4/26 15%
0/0 0%
Acute Myeloid Leukemia
7/90 8%
0/0 0%
Colorectal Carcinoma
36/143 25%
214/3239 7%
Non-Small Cell Lung Carcinoma
42/304 14%
82/1390 6%
Squamous Cell Lung Carcinoma
7/57 12%
55/810 7%
Gastric Carcinoma
8/74 11%
124/1809 7%
Other Solid Cancers
11/94 12%
93/1515 6%
Plasma Cell Myeloma
13/44 30%
7/305 2%
Cervical Carcinoma
1/35 3%
24/422 6%
Gastrointestinal Stromal Tumour
0/0 0%
7/133 5%
Unknown
1/10 10%
1/29 3%
Bladder Carcinoma
4/58 7%
44/956 5%
Hodgkins Lymphoma
4/16 25%
2/122 2%
Neuroendocrine Tumour
23/154 15%
7/577 1%
Ovarian Carcinoma
16/109 15%
28/998 3%
Other Sarcomas
7/69 10%
23/699 3%
Acute Monocytic Leukemia
1/1 100%
0/25 0%
Esophageal Squamous Cell Carcinoma
7/51 14%
79/2550 3%
Biliary Tract Carcinoma
1/54 2%
30/950 3%
Mesothelioma
5/62 8%
2/165 1%
Head and Neck Carcinoma
5/85 6%
46/1574 3%
Esophageal Carcinoma
3/23 13%
19/769 2%
Hepatocellular Carcinoma
5/46 11%
57/2210 3%
Non-Cancerous
3/104 3%
22/830 3%

Mutation Distribution

Where DNAH10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DNAH10 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 5,772 mutations in DNAH10

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