NFATC4 Nuclear factor of activated T cells 4 Q14934 NFAC4_HUMAN
Protein Coding Chr 14 14q12 Swiss-Prot reviewed Entrez 4776
Mutations
9,505
CL 589 · Tissue 8,755
Samples
525
CL 69 · Tissue 446
Peptides
438
unique mutant peptides
Transcripts
24
isoforms mutated

Stats by Source

Global, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Global = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Global can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

GlobalCell lineTissue
Mutations9,5055898,755
Samples52569446
Peptides43854392

Function

NFATC4 · Nuclear factor of activated T cells 4

This gene encodes a member of the nuclear factor of activated T cells (NFAT) protein family. The encoded protein is part of a DNA-binding transcription complex. This complex consists of at least two components: a preexisting cytosolic component that translocates to the nucleus upon T cell receptor stimulation and an inducible nuclear component. NFAT proteins are activated by the calmodulin-dependent phosphatase, calcineurin. The encoded protein plays a role in the inducible expression of cytokine genes in T cells, especially in the induction of interleukin-2 and interleukin-4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014].

Isoforms & Proteins

24 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
ENST00000250373 Q14934 540 377
ENST00000413692 Q14934-3 508 368
ENST00000556279 Q14934-4 504 362
ENST00000539237 Q14934-5 499 356
ENST00000555453 Q14934-9 498 360
ENST00000555590 Q14934-6 498 360
ENST00000422617 Q14934-10 493 354
ENST00000424781 Q14934-7 493 354
ENST00000553708 Q14934-8 493 354
ENST00000553879 Q14934-12 473 342
ENST00000554344 Q14934-12 473 342
ENST00000557451 Q14934-13 468 336
ENST00000554591 Q14934-11 441 327
ENST00000553469 Q14934-14 432 315
ENST00000554050 Q14934-16 426 313
ENST00000554966 Q14934-15 426 313
ENST00000556169 Q14934-17 426 313
ENST00000554661 Q14934-18 401 295
ENST00000556759 Q14934-19 254 185
ENST00000555167 Q14934-20 249 179
ENST00000554473 Q14934-21 182 138
ENST00000555802 Q14934-22 135 96
ENST00000555393 Q14934-23 130 90
ENST00000557767 Q14934-24 63 49

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q12
Entrez ID
Aliases
NF-AT3NF-ATC4NFAT3

Recurrent Mutations

Top recurrent amino-acid changes along the protein · needle height = number of mutations

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 Distribution

Where NFATC4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in NFATC4 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 9,505 mutations in NFATC4

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 CDSTypeSourcePeptide