KISS1R

KISS1 receptor Q969F8 KISSR_HUMAN
Protein Coding Chr 19 19p13.3 Swiss-Prot reviewed Entrez 84634
Mutations
191
CL 43 · Tissue 145
Samples
134
CL 36 · Tissue 96
Peptides
106
unique mutant peptides
Transcripts
2
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
Mutations19143145
Samples1343696
Peptides1063473

Function

KISS1R · KISS1 receptor

The protein encoded by this gene is a galanin-like G protein-coupled receptor that binds metastin, a peptide encoded by the metastasis suppressor gene KISS1. The tissue distribution of the expressed gene suggests that it is involved in the regulation of endocrine function, and this is supported by the finding that this gene appears to play a role in the onset of puberty. Mutations in this gene have been associated with hypogonadotropic hypogonadism and central precocious puberty. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

2 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
ENST00000234371 Q969F8 134 95
ENST00000606939 U3KQ86* 57 43

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p13.3
Entrez ID
Aliases
AXOR12CPPB1GPR54HH8HOT7T175KISS-1R

Recurrent Mutations

All 95 amino-acid changes on canonical ENST00000234371 · 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 KISS1R · 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 KISS1R – 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
8/40 20%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Glioblastoma
2/98 2%
0/0 0%
Thyroid Gland Carcinoma
0/45 0%
27/1592 2%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Endometrial Carcinoma
3/42 7%
2/612 0%
Neuroendocrine Tumour
3/154 2%
1/577 0%
Cervical Carcinoma
1/35 3%
1/422 0%
Gastric Carcinoma
0/74 0%
8/1809 0%
Pancreatic Carcinoma
1/89 1%
6/1611 0%
Glioma
0/52 0%
8/2127 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Ovarian Carcinoma
3/109 3%
1/998 0%
Non-Cancerous
1/104 1%
2/830 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Melanoma
1/210 0%
5/1899 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Non-Small Cell Lung Carcinoma
2/304 1%
2/1390 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Kidney Carcinoma
3/85 4%
1/1862 0%
Colorectal Carcinoma
1/143 1%
6/3239 0%
Prostate Carcinoma
1/13 8%
2/2105 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Sarcomas
0/69 0%
1/699 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
0/2550 0%
Neuroblastoma
1/87 1%
0/1331 0%
Breast Carcinoma
0/144 0%
2/3264 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%

Mutation Distribution

Where KISS1R is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KISS1R 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 49 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 191 mutations in KISS1R

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