ZC3H14

Zinc finger CCCH-type containing 14 Q6PJT7 ZC3HE_HUMAN
Protein Coding Chr 14 14q31.3 Swiss-Prot reviewed Entrez 79882
Mutations
2,403
CL 416 · Tissue 1,914
Samples
381
CL 87 · Tissue 282
Peptides
367
unique mutant peptides
Transcripts
10
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
Mutations2,4034161,914
Samples38187282
Peptides36767300

Function

ZC3H14 · Zinc finger CCCH-type containing 14

The protein encoded by this gene is a poly(A)-binding protein that can affect gene expression and poly(A) tail length. The encoded protein may influence mRNA stability, nuclear export, and translation. [provided by RefSeq, May 2016].

Isoforms & Proteins

10 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
ENST00000251038 Q6PJT7 377 273
ENST00000555755 Q6PJT7-9 331 254
ENST00000393514 Q6PJT7-5 327 250
ENST00000556945 G3V256* 264 213
ENST00000302216 Q6PJT7-3 258 207
ENST00000336693 Q6PJT7-4 254 204
ENST00000557607 G3V5I6* 187 152
ENST00000555900 G3V411* 183 139
ENST00000318308 Q6PJT7-6 114 96
ENST00000406216 Q6PJT7-8 108 90

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q31.3
Entrez ID
Aliases
MRT56MSUT-2NY-REN-37SUT2UKp68

Recurrent Mutations

All 273 amino-acid changes on canonical ENST00000251038 · 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 ZC3H14 · 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 ZC3H14 – 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
4/42 10%
23/612 4%
Glioblastoma
4/98 4%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Non-Small Cell Lung Carcinoma
13/304 4%
20/1390 1%
Melanoma
5/210 2%
35/1899 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Burkitts Lymphoma
4/32 12%
0/196 0%
Colorectal Carcinoma
16/143 11%
35/3239 1%
Osteosarcoma
3/45 7%
0/166 0%
Squamous Cell Lung Carcinoma
3/57 5%
9/810 1%
Bladder Carcinoma
2/58 3%
11/956 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Germ Cell Tumour
1/25 4%
1/169 1%
Gastric Carcinoma
3/74 4%
16/1809 1%
Other Solid Cancers
0/94 0%
16/1515 1%
Mesothelioma
1/62 2%
1/165 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Hepatocellular Carcinoma
0/46 0%
19/2210 1%
Other Sarcomas
1/69 1%
5/699 1%
Head and Neck Carcinoma
1/85 1%
11/1574 1%
Thyroid Gland Carcinoma
0/45 0%
11/1592 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
17/2550 1%
Biliary Tract Carcinoma
1/54 2%
5/950 1%
Neuroendocrine Tumour
2/154 1%
2/577 0%
Non-Cancerous
0/104 0%
5/830 1%
Esophageal Carcinoma
1/23 4%
3/769 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
B-Cell Non-Hodgkins Lymphoma
8/88 9%
4/2534 0%
Ovarian Carcinoma
0/109 0%
5/998 0%

Mutation Distribution

Where ZC3H14 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZC3H14 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 2,403 mutations in ZC3H14

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