HOOK1

Hook microtubule tethering protein 1 Q9UJC3 HOOK1_HUMAN
Protein Coding Chr 1 1p32.1 Swiss-Prot reviewed Entrez 51361
Mutations
327
CL 53 · Tissue 269
Samples
310
CL 52 · Tissue 255
Peptides
243
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
Mutations32753269
Samples31052255
Peptides24335207

Function

HOOK1 · Hook microtubule tethering protein 1

This gene encodes a member of the hook family of coiled-coil proteins, which bind to microtubules and organelles through their N- and C-terminal domains, respectively. The encoded protein localizes to discrete punctuate subcellular structures, and interacts with several members of the Rab GTPase family involved in endocytosis. It is thought to link endocytic membrane trafficking to the microtubule cytoskeleton. Several alternatively spliced transcript variants have been identified, but the full-length nature of some of these variants has not been determined. [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
ENST00000371208 Q9UJC3 327 243

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p32.1
Entrez ID
Aliases
HK1

Recurrent Mutations

All 243 amino-acid changes on canonical ENST00000371208 · 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 HOOK1 · 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 HOOK1 – 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
Glioblastoma
3/98 3%
0/0 0%
Endometrial Carcinoma
2/42 5%
16/612 3%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Chondrosarcoma
1/14 7%
1/75 1%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Colorectal Carcinoma
4/143 3%
52/3239 2%
Melanoma
0/210 0%
35/1899 2%
Squamous Cell Lung Carcinoma
0/57 0%
10/810 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Other Sarcomas
2/69 3%
6/699 1%
Gastric Carcinoma
5/74 7%
14/1809 1%
Non-Small Cell Lung Carcinoma
9/304 3%
5/1390 0%
Glioma
2/52 4%
14/2127 1%
Thyroid Gland Carcinoma
2/45 4%
10/1592 1%
Other Solid Cancers
3/94 3%
8/1515 1%
Breast Carcinoma
5/144 3%
17/3264 1%
Esophageal Carcinoma
0/23 0%
4/769 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Osteosarcoma
1/45 2%
0/166 0%
Esophageal Squamous Cell Carcinoma
3/51 6%
9/2550 0%
Medulloblastoma
0/0 0%
2/450 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Meningioma
1/3 33%
0/252 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
9/2534 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%

Mutation Distribution

Where HOOK1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HOOK1 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 327 mutations in HOOK1

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