DIPK1C

Divergent protein kinase domain 1C Q0P6D2 DIK1C_HUMAN
Protein Coding Chr 18 18q22.3 Swiss-Prot reviewed Entrez 125704
Mutations
345
CL 42 · Tissue 299
Samples
222
CL 33 · Tissue 186
Peptides
153
unique mutant peptides
Transcripts
2
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
Mutations34542299
Samples22233186
Peptides15328131

Function

DIPK1C · Divergent protein kinase domain 1C

This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. [provided by RefSeq, Nov 2011].

Isoforms & Proteins

2 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
ENST00000343998 Q0P6D2 242 146
ENST00000400291 Q0P6D2-2 103 62

Gene Properties

Type
Protein Coding
Chromosome
18
Cytoband
18q22.3
Entrez ID
Aliases
C18orf51FAM69CFNCAD

Recurrent Mutations

All 146 amino-acid changes on canonical ENST00000343998 · 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 DIPK1C · 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 DIPK1C – 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
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
2/42 5%
8/612 1%
Other Solid Cancers
1/94 1%
23/1515 2%
Colorectal Carcinoma
4/143 3%
34/3239 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Small Cell Lung Carcinoma
0/9 0%
7/752 1%
Cervical Carcinoma
1/35 3%
3/422 1%
Neuroendocrine Tumour
4/154 3%
2/577 0%
Bladder Carcinoma
1/58 2%
6/956 1%
Esophageal Squamous Cell Carcinoma
1/51 2%
16/2550 1%
Thyroid Gland Carcinoma
0/45 0%
10/1592 1%
Non-Small Cell Lung Carcinoma
2/304 1%
8/1390 1%
Gastric Carcinoma
2/74 3%
8/1809 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Head and Neck Carcinoma
1/85 1%
7/1574 0%
Non-Cancerous
0/104 0%
4/830 0%
Breast Carcinoma
1/144 1%
11/3264 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
8/2534 0%
Melanoma
2/210 1%
5/1899 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Neuroblastoma
1/87 1%
3/1331 0%
Medulloblastoma
0/0 0%
1/450 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Glioma
0/52 0%
3/2127 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Sarcomas
0/69 0%
1/699 0%
Pancreatic Carcinoma
1/89 1%
1/1611 0%

Mutation Distribution

Where DIPK1C is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DIPK1C 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.

Mutations

All 345 mutations in DIPK1C

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