ARHGAP35

Rho GTPase activating protein 35 Q9NRY4 RHG35_HUMAN
Protein Coding Chr 19 19q13.32 Swiss-Prot reviewed Entrez 2909
Mutations
920
CL 165 · Tissue 734
Samples
816
CL 139 · Tissue 662
Peptides
673
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
Mutations920165734
Samples816139662
Peptides673101576

Function

ARHGAP35 · Rho GTPase activating protein 35

The human glucocorticoid receptor DNA binding factor, which associates with the promoter region of the glucocorticoid receptor gene (hGR gene), is a repressor of glucocorticoid receptor transcription. The amino acid sequence deduced from the cDNA sequences show the presence of three sequence motifs characteristic of a zinc finger and one motif suggestive of a leucine zipper in which 1 cysteine is found instead of all leucines. The GRLF1 enhances the homologous down-regulation of wild-type hGR gene expression. Biochemical analysis suggests that GRLF1 interaction is sequence specific and that transcriptional efficacy of GRLF1 is regulated through its interaction with specific sequence motif. The level of expression is regulated by glucocorticoids. [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
ENST00000672722 Q9NRY4 920 673

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.32
Entrez ID
Aliases
GRF-1GRLF1P190-AP190Ap190ARhoGAPp190RhoGAP

Recurrent Mutations

All 673 amino-acid changes on canonical ENST00000672722 · 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 ARHGAP35 · 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 ARHGAP35 – 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
T-Lymphoblastic Leukemia
9/40 22%
0/0 0%
Chronic Myelogenous Leukemia
3/25 12%
0/0 0%
Endometrial Carcinoma
11/42 26%
47/612 8%
Hodgkins Lymphoma
2/16 12%
5/122 4%
Melanoma
6/210 3%
78/1899 4%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Retinoblastoma
1/27 4%
1/30 3%
Squamous Cell Lung Carcinoma
4/57 7%
23/810 3%
Colorectal Carcinoma
18/143 13%
87/3239 3%
Bladder Carcinoma
0/58 0%
30/956 3%
Cervical Carcinoma
0/35 0%
12/422 3%
Unknown
0/10 0%
1/29 3%
Non-Small Cell Lung Carcinoma
5/304 2%
37/1390 3%
Small Cell Lung Carcinoma
0/9 0%
17/752 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Burkitts Lymphoma
0/32 0%
5/196 3%
Other Solid Cancers
4/94 4%
31/1515 2%
Gastric Carcinoma
1/74 1%
38/1809 2%
Neuroendocrine Tumour
8/154 5%
7/577 1%
Glioblastoma
2/98 2%
0/0 0%
Hepatocellular Carcinoma
5/46 11%
35/2210 2%
Mesothelioma
3/62 5%
1/165 1%
Ovarian Carcinoma
6/109 6%
12/998 1%
Head and Neck Carcinoma
2/85 2%
23/1574 1%
Other Sarcomas
3/69 4%
8/699 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
32/2550 1%
Glioma
1/52 2%
24/2127 1%
Breast Carcinoma
7/144 5%
29/3264 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Biliary Tract Carcinoma
1/54 2%
9/950 1%

Mutation Distribution

Where ARHGAP35 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ARHGAP35 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 920 mutations in ARHGAP35

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