LHB

Luteinizing hormone subunit beta P01229 LSHB_HUMAN
Protein Coding Chr 19 19q13.33 Swiss-Prot reviewed Entrez 3972
Mutations
74
CL 14 · Tissue 60
Samples
69
CL 14 · Tissue 55
Peptides
59
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
Mutations741460
Samples691455
Peptides59951

Function

LHB · Luteinizing hormone subunit beta

This gene is a member of the glycoprotein hormone beta chain family and encodes the beta subunit of luteinizing hormone (LH). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. LH is expressed in the pituitary gland and promotes spermatogenesis and ovulation by stimulating the testes and ovaries to synthesize steroids. The genes for the beta chains of chorionic gonadotropin and for luteinizing hormone are contiguous on chromosome 19q13.3. Mutations in this gene are associated with hypogonadism which is characterized by infertility and pseudohermaphroditism. [provided by RefSeq, Jul 2008].

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
ENST00000649238 P01229 74 59

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.33
Entrez ID
Aliases
CGB4HH23LSH-BLSH-beta

Recurrent Mutations

All 59 amino-acid changes on canonical ENST00000649238 · 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 LHB · 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 LHB – 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
Plasma Cell Myeloma
2/44 5%
0/305 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Endometrial Carcinoma
0/42 0%
2/612 0%
Bladder Carcinoma
1/58 2%
2/956 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
5/2550 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Non-Small Cell Lung Carcinoma
1/304 0%
3/1390 0%
Melanoma
0/210 0%
5/1899 0%
Colorectal Carcinoma
2/143 1%
6/3239 0%
Squamous Cell Lung Carcinoma
1/57 2%
1/810 0%
Gastric Carcinoma
0/74 0%
4/1809 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Ovarian Carcinoma
2/109 2%
0/998 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Other Solid Cancers
0/94 0%
2/1515 0%
Non-Cancerous
1/104 1%
0/830 0%
Kidney Carcinoma
1/85 1%
1/1862 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Glioma
0/52 0%
2/2127 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Prostate Carcinoma
0/13 0%
1/2105 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in LHB 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 74 mutations in LHB

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