PARD3 Par-3 family cell polarity regulator Q8TEW0 PARD3_HUMAN
Protein Coding Chr 10 10p11.22-p11.21 Swiss-Prot reviewed Entrez 56288
Mutations
7,588
CL 765 · Tissue 6,704
Samples
721
CL 119 · Tissue 592
Peptides
641
unique mutant peptides
Transcripts
13
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
Mutations7,5887656,704
Samples721119592
Peptides641101553

Function

PARD3 · Par-3 family cell polarity regulator

This gene encodes a member of the PARD protein family. PARD family members interact with other PARD family members and other proteins; they affect asymmetrical cell division and direct polarized cell growth. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011].

Isoforms & Proteins

13 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
ENST00000374788 Q8TEW0-2 796 550
ENST00000374789 Q8TEW0 727 534
ENST00000545693 Q8TEW0-11 720 528
ENST00000350537 Q8TEW0-6 706 517
ENST00000346874 Q8TEW0-4 705 520
ENST00000374790 Q5VWV2* 695 509
ENST00000545260 Q8TEW0-3 681 498
ENST00000374794 Q8TEW0-5 664 489
ENST00000340077 Q8TEW0-8 490 366
ENST00000374773 Q5VWU8* 476 355
ENST00000374776 Q8TEW0-9 472 351
ENST00000544292 F5GZI3* 376 277
ENST00000374768 B1AP52* 80 65

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10p11.22-p11.21
Entrez ID
Aliases
ASIPBazPAR3PAR3alphaPARD-3PARD3A

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 PARD3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PARD3 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 7,588 mutations in PARD3

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