MED14

Mediator complex subunit 14 O60244 MED14_HUMAN
Protein Coding Chr X Xp11.4 Swiss-Prot reviewed Entrez 9282
Mutations
547
CL 90 · Tissue 440
Samples
486
CL 82 · Tissue 396
Peptides
411
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
Mutations54790440
Samples48682396
Peptides41161350

Function

MED14 · Mediator complex subunit 14

The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. This protein contains a bipartite nuclear localization signal. This gene is known to escape chromosome X-inactivation. [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
ENST00000324817 O60244 547 411

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xp11.4
Entrez ID
Aliases
CRSP150CRSP2CSRPCXorf4DRIP150EXLM1

Recurrent Mutations

All 412 amino-acid changes on canonical ENST00000324817 · 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 MED14 · 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 MED14 – 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
3/40 8%
0/0 0%
Endometrial Carcinoma
5/42 12%
44/612 7%
Melanoma
3/210 1%
61/1899 3%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Squamous Cell Lung Carcinoma
6/57 11%
12/810 1%
Colorectal Carcinoma
11/143 8%
49/3239 2%
Cervical Carcinoma
0/35 0%
8/422 2%
Burkitts Lymphoma
3/32 9%
1/196 1%
Non-Small Cell Lung Carcinoma
12/304 4%
14/1390 1%
Gastric Carcinoma
1/74 1%
26/1809 1%
Hepatocellular Carcinoma
1/46 2%
25/2210 1%
Neuroendocrine Tumour
4/154 3%
4/577 1%
Germ Cell Tumour
1/25 4%
1/169 1%
Glioblastoma
1/98 1%
0/0 0%
Bladder Carcinoma
0/58 0%
10/956 1%
Thyroid Gland Carcinoma
0/45 0%
16/1592 1%
Other Solid Cancers
0/94 0%
15/1515 1%
Head and Neck Carcinoma
2/85 2%
13/1574 1%
Kidney Carcinoma
0/85 0%
17/1862 1%
Non-Cancerous
1/104 1%
7/830 1%
Other Sarcomas
0/69 0%
6/699 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Breast Carcinoma
5/144 3%
19/3264 1%
Glioma
0/52 0%
14/2127 1%
Ovarian Carcinoma
5/109 5%
2/998 0%
Esophageal Carcinoma
2/23 9%
3/769 0%
Plasma Cell Myeloma
1/44 2%
1/305 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Mesothelioma
1/62 2%
0/165 0%
Biliary Tract Carcinoma
1/54 2%
3/950 0%

Mutation Distribution

Where MED14 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MED14 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 547 mutations in MED14

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