JHY

Junctional cadherin complex regulator Q6NUN7 JHY_HUMAN
Protein Coding Chr 11 11q24.1 Swiss-Prot reviewed Entrez 79864
Mutations
1,225
CL 142 · Tissue 1,073
Samples
489
CL 75 · Tissue 409
Peptides
366
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
Mutations1,2251421,073
Samples48975409
Peptides36652323

Function

JHY · Junctional cadherin complex regulator

Predicted to be involved in axoneme assembly and brain development. Predicted to act upstream of or within several processes, including cerebrospinal fluid circulation; motile cilium assembly; and regulation of establishment of planar polarity. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000227349 Q6NUN7 522 355
ENST00000531316 Q6NUN7 481 345
ENST00000307257 Q6NUN7-2 222 157

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q24.1
Entrez ID
Aliases
C11orf63

Recurrent Mutations

All 355 amino-acid changes on canonical ENST00000227349 · 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 JHY · 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 JHY – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Endometrial Carcinoma
6/42 14%
23/612 4%
Non-Small Cell Lung Carcinoma
15/304 5%
28/1390 2%
Melanoma
1/210 0%
51/1899 3%
Gastric Carcinoma
3/74 4%
41/1809 2%
Small Cell Lung Carcinoma
0/9 0%
17/752 2%
Other Solid Cancers
2/94 2%
33/1515 2%
Germ Cell Tumour
3/25 12%
1/169 1%
Colorectal Carcinoma
9/143 6%
56/3239 2%
Squamous Cell Lung Carcinoma
0/57 0%
15/810 2%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Chondrosarcoma
1/14 7%
0/75 0%
Cervical Carcinoma
0/35 0%
5/422 1%
Bladder Carcinoma
1/58 2%
10/956 1%
Glioblastoma
1/98 1%
0/0 0%
Neuroendocrine Tumour
4/154 3%
3/577 1%
Biliary Tract Carcinoma
0/54 0%
9/950 1%
Mesothelioma
0/62 0%
2/165 1%
Non-Cancerous
2/104 2%
6/830 1%
Hepatocellular Carcinoma
1/46 2%
18/2210 1%
Kidney Carcinoma
3/85 4%
10/1862 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
15/2550 1%
Esophageal Carcinoma
1/23 4%
4/769 1%
Ovarian Carcinoma
0/109 0%
7/998 1%
Head and Neck Carcinoma
3/85 4%
7/1574 0%
Thyroid Gland Carcinoma
1/45 2%
8/1592 0%
Breast Carcinoma
4/144 3%
11/3264 0%
Glioma
0/52 0%
9/2127 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in JHY 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 1,225 mutations in JHY

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