BLNK

B cell linker Q8WV28 BLNK_HUMAN
Protein Coding Chr 10 10q24.1 Swiss-Prot reviewed Entrez 29760
Mutations
758
CL 116 · Tissue 640
Samples
218
CL 45 · Tissue 171
Peptides
209
unique mutant peptides
Transcripts
5
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
Mutations758116640
Samples21845171
Peptides20939176

Function

BLNK · B cell linker

This gene encodes a cytoplasmic linker or adaptor protein that plays a critical role in B cell development. This protein bridges B cell receptor-associated kinase activation with downstream signaling pathways, thereby affecting various biological functions. The phosphorylation of five tyrosine residues is necessary for this protein to nucleate distinct signaling effectors following B cell receptor activation. Mutations in this gene cause hypoglobulinemia and absent B cells, a disease in which the pro- to pre-B-cell transition is developmentally blocked. Deficiency in this protein has also been shown in some cases of pre-B acute lymphoblastic leukemia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012].

Isoforms & Proteins

5 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
ENST00000224337 Q8WV28 231 176
ENST00000371176 Q8WV28-2 196 158
ENST00000413476 Q8WV28-3 183 150
ENST00000427367 A0ACM8Q980* 128 102
ENST00000495266 K7EKR2* 20 20

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q24.1
Entrez ID
Aliases
AGM4BASHBLNK-SLY57SLP-65SLP65

Recurrent Mutations

All 176 amino-acid changes on canonical ENST00000224337 · 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 BLNK · 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 BLNK – 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%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Melanoma
8/210 4%
53/1899 3%
Endometrial Carcinoma
3/42 7%
11/612 2%
Germ Cell Tumour
2/25 8%
1/169 1%
Chondrosarcoma
0/14 0%
1/75 1%
Glioblastoma
1/98 1%
0/0 0%
Bladder Carcinoma
0/58 0%
10/956 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Colorectal Carcinoma
12/143 8%
14/3239 0%
Non-Small Cell Lung Carcinoma
3/304 1%
10/1390 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Squamous Cell Lung Carcinoma
0/57 0%
6/810 1%
Gastric Carcinoma
3/74 4%
9/1809 0%
Ewings Sarcoma
1/63 2%
1/262 0%
Other Solid Cancers
0/94 0%
10/1515 1%
Other Sarcomas
0/69 0%
4/699 1%
Osteosarcoma
1/45 2%
0/166 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Mesothelioma
0/62 0%
1/165 1%
Meningioma
1/3 33%
0/252 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Glioma
3/52 6%
3/2127 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Neuroblastoma
0/87 0%
2/1331 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in BLNK 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 758 mutations in BLNK

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