IGLL5

Immunoglobulin lambda like polypeptide 5 B9A064 IGLL5_HUMAN
Protein Coding Chr 22 22q11.22 Swiss-Prot reviewed Entrez 100423062
Mutations
1,598
CL 78 · Tissue 1,520
Samples
455
CL 50 · Tissue 405
Peptides
393
unique mutant peptides
Transcripts
3
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
Mutations1,598781,520
Samples45550405
Peptides39341366

Function

IGLL5 · Immunoglobulin lambda like polypeptide 5

This gene encodes one of the immunoglobulin lambda-like polypeptides. It is located within the immunoglobulin lambda locus but it does not require somatic rearrangement for expression. The first exon of this gene is unrelated to immunoglobulin variable genes; the second and third exons are the immunoglobulin lambda joining 1 and the immunoglobulin lambda constant 1 gene segments. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010].

Isoforms & Proteins

3 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
ENST00000526893 B9A064 612 304
ENST00000532223 A0A0B4J231* 588 293
ENST00000531372 B9A064-2 398 178

Gene Properties

Type
Protein Coding
Chromosome
22
Cytoband
22q11.22
Entrez ID
Aliases
IGLVVL-MAR

Recurrent Mutations

All 304 amino-acid changes on canonical ENST00000526893 · 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 IGLL5 · 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 IGLL5 – 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
Hodgkins Lymphoma
4/16 25%
37/122 30%
Burkitts Lymphoma
3/32 9%
27/196 14%
B-Cell Non-Hodgkins Lymphoma
6/88 7%
166/2534 7%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Plasma Cell Myeloma
1/44 2%
8/305 3%
Other Blood Cancers
3/61 5%
51/2725 2%
Glioblastoma
1/98 1%
0/0 0%
Osteosarcoma
2/45 4%
0/166 0%
Non-Small Cell Lung Carcinoma
10/304 3%
6/1390 0%
Melanoma
0/210 0%
18/1899 1%
Endometrial Carcinoma
0/42 0%
5/612 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Colorectal Carcinoma
3/143 2%
20/3239 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Squamous Cell Lung Carcinoma
2/57 4%
3/810 0%
Other Solid Cancers
1/94 1%
8/1515 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Neuroendocrine Tumour
3/154 2%
0/577 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Gastric Carcinoma
2/74 3%
5/1809 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Thyroid Gland Carcinoma
1/45 2%
4/1592 0%
Bladder Carcinoma
2/58 3%
1/956 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
7/2550 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Glioma
0/52 0%
5/2127 0%
Biliary Tract Carcinoma
1/54 2%
1/950 0%
Breast Carcinoma
0/144 0%
5/3264 0%

Mutation Distribution

Where IGLL5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IGLL5 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.

Mutations

All 1,598 mutations in IGLL5

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