KIAA1217

KIAA1217 Q5T5P2 SKT_HUMAN
Protein Coding Chr 10 10p12.2-p12.1 Swiss-Prot reviewed Entrez 56243
Mutations
6,948
CL 907 · Tissue 5,939
Samples
1,029
CL 188 · Tissue 817
Peptides
907
unique mutant peptides
Transcripts
11
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
Mutations6,9489075,939
Samples1,029188817
Peptides907149768

Function

KIAA1217 · KIAA1217

Predicted to be involved in embryonic skeletal system development. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

11 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
ENST00000376454 Q5T5P2 1,210 843
ENST00000376451 Q5T5P2-3 843 612
ENST00000376452 Q5T5P2-10 833 602
ENST00000458595 Q5T5P2-7 813 593
ENST00000376462 Q5T5P2-9 760 558
ENST00000430453 Q5T5P2-9 759 556
ENST00000307544 Q5T5P2-6 596 427
ENST00000396445 Q5T5P2-8 575 417
ENST00000396446 Q5T5P2-4 557 402
ENST00000635504 A0A0U1RQK8* 1 1
ENST00000636305 A0A1B0GU17* 1 1

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10p12.2-p12.1
Entrez ID
Aliases
ETL4SKT

Recurrent Mutations

All 843 amino-acid changes on canonical ENST00000376454 · 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 KIAA1217 · 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 KIAA1217 – 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
9/40 22%
0/0 0%
Chronic Myelogenous Leukemia
4/25 16%
0/0 0%
Melanoma
22/210 10%
193/1899 10%
Endometrial Carcinoma
9/42 21%
48/612 8%
Hodgkins Lymphoma
2/16 12%
4/122 3%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Colorectal Carcinoma
22/143 15%
99/3239 3%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Glioblastoma
3/98 3%
0/0 0%
Bladder Carcinoma
1/58 2%
30/956 3%
Non-Small Cell Lung Carcinoma
22/304 7%
28/1390 2%
Other Solid Cancers
1/94 1%
44/1515 3%
Ewings Sarcoma
3/63 5%
6/262 2%
Cervical Carcinoma
2/35 6%
10/422 2%
Burkitts Lymphoma
6/32 19%
0/196 0%
Unknown
1/10 10%
0/29 0%
Gastric Carcinoma
1/74 1%
46/1809 3%
Hepatocellular Carcinoma
1/46 2%
52/2210 2%
Non-Cancerous
2/104 2%
16/830 2%
Squamous Cell Lung Carcinoma
3/57 5%
13/810 2%
Head and Neck Carcinoma
6/85 7%
24/1574 2%
Other Sarcomas
4/69 6%
8/699 1%
Germ Cell Tumour
1/25 4%
2/169 1%
Ovarian Carcinoma
6/109 6%
11/998 1%
Esophageal Carcinoma
0/23 0%
12/769 2%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Plasma Cell Myeloma
3/44 7%
2/305 1%
Biliary Tract Carcinoma
2/54 4%
12/950 1%
Small Cell Lung Carcinoma
1/9 11%
9/752 1%
Glioma
1/52 2%
26/2127 1%

Mutation Distribution

Where KIAA1217 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KIAA1217 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 6,948 mutations in KIAA1217

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