NDRG2 NDRG family member 2 Q9UN36 NDRG2_HUMAN
Protein Coding Chr 14 14q11.2 Swiss-Prot reviewed Entrez 57447
Mutations
2,219
CL 170 · Tissue 2,004
Samples
161
CL 27 · Tissue 131
Peptides
181
unique mutant peptides
Transcripts
15
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
Mutations2,2191702,004
Samples16127131
Peptides18127150

Function

NDRG2 · NDRG family member 2

This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein that may play a role in neurite outgrowth. This gene may be involved in glioblastoma carcinogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017].

Isoforms & Proteins

15 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
ENST00000556147 Q9UN36 167 122
ENST00000350792 Q9UN36-2 165 120
ENST00000298687 Q9UN36 154 116
ENST00000403829 Q9UN36-6 151 114
ENST00000397851 Q9UN36 149 112
ENST00000397853 Q9UN36 149 112
ENST00000397858 Q9UN36 149 112
ENST00000360463 Q9UN36-2 147 110
ENST00000397847 Q9UN36-3 147 110
ENST00000553503 Q9UN36-2 147 110
ENST00000554143 Q9UN36-2 147 110
ENST00000555158 Q9UN36-2 147 110
ENST00000397844 Q9UN36-5 144 109
ENST00000298684 Q9UN36-4 138 102
ENST00000554104 G3V578* 118 85

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q11.2
Entrez ID
Aliases
SYLD

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 NDRG2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in NDRG2 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 2,219 mutations in NDRG2

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