CFAP54

Cilia and flagella associated protein 54 Q96N23 CFA54_HUMAN
Protein Coding Chr 12 12q23.1 Swiss-Prot reviewed Entrez 144535
Mutations
1,347
CL 333 · Tissue 1,006
Samples
1,093
CL 274 · Tissue 812
Peptides
942
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
Mutations1,3473331,006
Samples1,093274812
Peptides942222755

Function

CFAP54 · Cilia and flagella associated protein 54

Predicted to be involved in cilium assembly; cilium movement involved in cell motility; and spermatogenesis. Predicted to act upstream of or within cerebrospinal fluid circulation; motile cilium assembly; and mucociliary clearance. Predicted to be located in axoneme. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000524981 Q96N23 1,347 942

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q23.1
Entrez ID
Aliases
C12orf55C12orf63CILD54SPGF98

Recurrent Mutations

All 943 amino-acid changes on canonical ENST00000524981 · 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 CFAP54 · 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 CFAP54 – 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
Glioblastoma
13/98 13%
0/0 0%
Melanoma
37/210 18%
235/1899 12%
T-Lymphoblastic Leukemia
5/40 12%
0/0 0%
Oral Cavity Carcinoma
5/54 9%
0/0 0%
Endometrial Carcinoma
15/42 36%
44/612 7%
Non-Small Cell Lung Carcinoma
35/304 12%
45/1390 3%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Gastric Carcinoma
8/74 11%
59/1809 3%
Colorectal Carcinoma
35/143 24%
84/3239 3%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Cervical Carcinoma
1/35 3%
12/422 3%
Squamous Cell Lung Carcinoma
5/57 9%
18/810 2%
Hepatocellular Carcinoma
7/46 15%
51/2210 2%
Bladder Carcinoma
7/58 12%
17/956 2%
Other Sarcomas
6/69 9%
12/699 2%
Mesothelioma
4/62 6%
1/165 1%
Other Solid Cancers
7/94 7%
26/1515 2%
Biliary Tract Carcinoma
4/54 7%
16/950 2%
Adrenocortical Carcinoma
2/3 67%
0/112 0%
Plasma Cell Myeloma
5/44 11%
1/305 0%
Thyroid Gland Carcinoma
1/45 2%
27/1592 2%
Esophageal Carcinoma
4/23 17%
9/769 1%
Small Cell Lung Carcinoma
0/9 0%
12/752 2%
Neuroendocrine Tumour
6/154 4%
5/577 1%
Esophageal Squamous Cell Carcinoma
9/51 18%
29/2550 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Head and Neck Carcinoma
3/85 4%
14/1574 1%
Ovarian Carcinoma
6/109 6%
5/998 0%
Rhabdomyosarcoma
1/33 3%
1/171 1%
Glioma
4/52 8%
14/2127 1%

Mutation Distribution

Where CFAP54 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CFAP54 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 1,347 mutations in CFAP54

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