Stats by Source
Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)
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.
| Total | Cell line | Tissue | |
|---|---|---|---|
| Mutations | 3,549 | 404 | 3,092 |
| Samples | 1,087 | 188 | 886 |
| Peptides | 880 | 125 | 777 |
Function
NEXMIF · Neurite extension and migration factor
An inversion on the X chromosome which disrupts this gene and a G-protein coupled purinergic receptor gene located in the pseudoautosomal region of the X chromosome has been linked to X linked cognitive disability.[provided by RefSeq, Mar 2009].
Isoforms & Proteins
3 transcripts · UniProt mapping is sequence-verified (AA-safe)
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.
| Transcript | UniProt | Mutations | Peptides |
|---|---|---|---|
| ENST00000055682 | Q5QGS0 | 1,261 | 872 |
| ENST00000616200 | Q5QGS0 | 1,155 | 844 |
| ENST00000642681 | A0A2R8YEQ5* | 1,133 | 824 |
Gene Properties
Recurrent Mutations
All 872 amino-acid changes on canonical ENST00000055682 · needle height = samples · drag the mini-map to zoom
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 NEXMIF · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in NEXMIF – 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 type | Cell lines | Tissue samples |
|---|---|---|
| T-Lymphoblastic Leukemia | 7/40 18% | 0/0 0% |
| Melanoma | 31/210 15% | 249/1899 13% |
| Chronic Myelogenous Leukemia | 3/25 12% | 0/0 0% |
| Glioblastoma | 7/98 7% | 0/0 0% |
| Endometrial Carcinoma | 8/42 19% | 37/612 6% |
| Non-Small Cell Lung Carcinoma | 24/304 8% | 55/1390 4% |
| Squamous Cell Lung Carcinoma | 2/57 4% | 36/810 4% |
| T-Cell Non-Hodgkins Lymphoma | 1/26 4% | 0/0 0% |
| Gastric Carcinoma | 6/74 8% | 66/1809 4% |
| Oral Cavity Carcinoma | 2/54 4% | 0/0 0% |
| Hodgkins Lymphoma | 2/16 12% | 3/122 2% |
| Colorectal Carcinoma | 24/143 17% | 97/3239 3% |
| Cervical Carcinoma | 3/35 9% | 11/422 3% |
| Other Solid Cancers | 5/94 5% | 38/1515 3% |
| Ovarian Carcinoma | 13/109 12% | 11/998 1% |
| Head and Neck Carcinoma | 5/85 6% | 30/1574 2% |
| Bladder Carcinoma | 0/58 0% | 21/956 2% |
| Small Cell Lung Carcinoma | 0/9 0% | 14/752 2% |
| Other Sarcomas | 3/69 4% | 11/699 2% |
| Neuroendocrine Tumour | 9/154 6% | 4/577 1% |
| Esophageal Carcinoma | 4/23 17% | 10/769 1% |
| Rhabdomyosarcoma | 3/33 9% | 0/171 0% |
| Hepatocellular Carcinoma | 0/46 0% | 33/2210 1% |
| Esophageal Squamous Cell Carcinoma | 0/51 0% | 36/2550 1% |
| Burkitts Lymphoma | 3/32 9% | 0/196 0% |
| Biliary Tract Carcinoma | 1/54 2% | 12/950 1% |
| Breast Carcinoma | 3/144 2% | 37/3264 1% |
| Germ Cell Tumour | 0/25 0% | 2/169 1% |
| Mesothelioma | 1/62 2% | 1/165 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 1/133 1% |
Mutation Distribution
Where NEXMIF is mutated · all tissues, split by cell line vs tissue
How many mutations in NEXMIF 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 3,549 mutations in NEXMIF
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.
| ID | Sample | Transcript | AA Change | CDS | Type | Source | Mutant Peptide | Wild-type Peptide |
|---|