CUX1 Cut like homeobox 1 P39880 CUX1_HUMAN
Protein Coding Chr 7 7q22.1 Swiss-Prot reviewed Entrez 1523
Mutations
8,306
CL 789 · Tissue 7,392
Samples
968
CL 170 · Tissue 785
Peptides
798
unique mutant peptides
Transcripts
14
isoforms mutated

Stats by Source

Global, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Global = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Global can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

GlobalCell lineTissue
Mutations8,3067897,392
Samples968170785
Peptides798141675

Function

CUX1 · Cut like homeobox 1

The protein encoded by this gene is a member of the homeodomain family of DNA binding proteins. It may regulate gene expression, morphogenesis, and differentiation and it may also play a role in the cell cycle progession. Several alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Feb 2011].

Isoforms & Proteins

14 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
ENST00000292535 P39880 892 616
ENST00000360264 P39880-3 798 573
ENST00000546411 P39880 795 570
ENST00000549414 P39880-2 780 561
ENST00000645010 A0A2R8Y852* 773 554
ENST00000550008 P39880-5 770 551
ENST00000646649 A0A2R8YDI1* 713 508
ENST00000556210 P39880-6 710 505
ENST00000622516 Q13948 367 257
ENST00000292538 Q13948 354 253
ENST00000437600 Q13948-2 353 252
ENST00000547394 Q13948-10 346 247
ENST00000425244 P39880-9 340 240
ENST00000393824 Q13948-9 315 231

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7q22.1
Entrez ID
Aliases
CASPCDPCDP/CutCDP1COY1CUTL1

Recurrent Mutations

Top recurrent amino-acid changes along the protein · needle height = number of mutations

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 Distribution

Where CUX1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CUX1 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 8,306 mutations in CUX1

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 CDSTypeSourcePeptide