RASL10A
geneOn this page
Also known as RRP22
Summary
RASL10A (RAS like family 10 member A, HGNC:16954) is a protein-coding gene on chromosome 22q12.2, encoding Ras-like protein family member 10A (Q92737). Potent inhibitor of cellular proliferation.
Predicted to enable GTPase activity. Predicted to be involved in small GTPase-mediated signal transduction. Predicted to be located in nucleolus and plasma membrane.
Source: NCBI Gene 10633 — RefSeq curated summary.
At a glance
- GWAS associations: 3
- Clinical variants (ClinVar): 27 total
- MANE Select transcript:
NM_006477
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:16954 |
| Approved symbol | RASL10A |
| Name | RAS like family 10 member A |
| Location | 22q12.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | RRP22 |
| Ensembl gene | ENSG00000100276 |
| Ensembl biotype | protein_coding |
| OMIM | 602220 |
| Entrez | 10633 |
Gene structure
Transcript identifiers
Ensembl transcripts: 6 — 4 protein_coding, 2 protein_coding_CDS_not_defined
ENST00000216101, ENST00000401450, ENST00000474590, ENST00000608559, ENST00000942940, ENST00000942941
RefSeq mRNA: 1 — MANE Select: NM_006477
NM_006477
CCDS: CCDS13854
Canonical transcript exons
ENST00000216101 — 3 exons
| Exon | Start | End |
|---|---|---|
| ENSE00000652040 | 29313863 | 29313987 |
| ENSE00000879733 | 29315028 | 29315697 |
| ENSE00001326105 | 29312933 | 29313568 |
Expression profiles
Bgee: expression breadth ubiquitous, 183 present calls, max score 89.54.
FANTOM5 (CAGE): breadth broad, TPM avg 1.2224 / max 66.7850, expressed in 320 samples.
FANTOM5 promoters (5 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 193518 | 0.7043 | 254 |
| 193517 | 0.2978 | 77 |
| 193519 | 0.1565 | 84 |
| 193515 | 0.0420 | 28 |
| 193516 | 0.0218 | 16 |
Top tissues by expression
288 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| amygdala | UBERON:0001876 | 89.54 | gold quality |
| middle temporal gyrus | UBERON:0002771 | 88.16 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 88.02 | gold quality |
| right frontal lobe | UBERON:0002810 | 87.66 | gold quality |
| cingulate cortex | UBERON:0003027 | 87.23 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 87.11 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 87.06 | gold quality |
| temporal lobe | UBERON:0001871 | 87.02 | gold quality |
| cortical plate | UBERON:0005343 | 86.54 | gold quality |
| prefrontal cortex | UBERON:0000451 | 85.77 | gold quality |
| frontal cortex | UBERON:0001870 | 84.86 | gold quality |
| neocortex | UBERON:0001950 | 84.81 | gold quality |
| nucleus accumbens | UBERON:0001882 | 84.65 | gold quality |
| cerebral cortex | UBERON:0000956 | 84.35 | gold quality |
| caudate nucleus | UBERON:0001873 | 84.26 | gold quality |
| entorhinal cortex | UBERON:0002728 | 84.22 | gold quality |
| Brodmann (1909) area 46 | UBERON:0006483 | 83.92 | gold quality |
| telencephalon | UBERON:0001893 | 83.80 | gold quality |
| orbitofrontal cortex | UBERON:0004167 | 83.79 | gold quality |
| putamen | UBERON:0001874 | 83.39 | gold quality |
| Ammon’s horn | UBERON:0001954 | 83.02 | gold quality |
| forebrain | UBERON:0001890 | 82.88 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 82.18 | gold quality |
| primary visual cortex | UBERON:0002436 | 82.06 | gold quality |
| Brodmann (1909) area 10 | UBERON:0013541 | 81.84 | silver quality |
| hypothalamus | UBERON:0001898 | 81.82 | gold quality |
| endothelial cell | CL:0000115 | 81.31 | silver quality |
| CA1 field of hippocampus | UBERON:0003881 | 80.89 | gold quality |
| brain | UBERON:0000955 | 80.75 | gold quality |
| central nervous system | UBERON:0001017 | 80.50 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.88 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
18 targeting RASL10A, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-186-5P | 99.99 | 70.83 | 3707 |
| HSA-MIR-204-5P | 99.79 | 71.62 | 2439 |
| HSA-MIR-211-5P | 99.79 | 71.65 | 2440 |
| HSA-MIR-4446-5P | 99.72 | 69.19 | 2544 |
| HSA-MIR-4755-5P | 99.71 | 70.34 | 2716 |
| HSA-MIR-5006-3P | 99.71 | 70.26 | 2728 |
| HSA-MIR-6086 | 99.70 | 65.38 | 699 |
| HSA-MIR-6832-3P | 99.52 | 70.44 | 1726 |
| HSA-MIR-3688-5P | 99.12 | 69.67 | 1091 |
| HSA-MIR-891A-3P | 98.05 | 67.99 | 970 |
| HSA-MIR-6072 | 98.00 | 66.47 | 804 |
| HSA-MIR-6762-5P | 96.55 | 64.62 | 972 |
| HSA-MIR-6845-5P | 96.55 | 64.65 | 969 |
| HSA-MIR-7973 | 96.48 | 65.54 | 502 |
| HSA-MIR-644A | 96.02 | 66.52 | 786 |
| HSA-MIR-6891-3P | 95.80 | 65.76 | 683 |
| HSA-MIR-6874-5P | 95.73 | 64.94 | 545 |
| HSA-MIR-1247-5P | 85.92 | 61.07 | 65 |
Literature-anchored findings (GeneRIF, showing 4)
- RRP22 localizes to the nucleolus in a GTP-dependent manner and can serve as a potential tumor suppressor. (PMID:15833841)
- chromosome 22 have specific motor deficits in axial stability and graphomotor skills. (PMID:20646714)
- RRP22 is a special neural tumor suppressor for human astrocytomas (PMID:21264544)
- Both 5’-CpG island hypermethylation and histone modifications contribute to the frequent and prognostically unfavorable transcriptional downregulation of RRP22 in malignant gliomas. (PMID:21631628)
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Rasl10a | ENSMUSG00000034209 |
| rattus_norvegicus | Rasl10a | ENSRNOG00000008951 |
Paralogs (35): RALA (ENSG00000006451), REM1 (ENSG00000088320), RASD2 (ENSG00000100302), RASL12 (ENSG00000103710), RHEB (ENSG00000106615), RASD1 (ENSG00000108551), RERGL (ENSG00000111404), RAP1A (ENSG00000116473), RASL11A (ENSG00000122035), RAP2C (ENSG00000123728), RAP2A (ENSG00000125249), RRAS (ENSG00000126458), RAP1B (ENSG00000127314), RASL11B (ENSG00000128045), KRAS (ENSG00000133703), RRAS2 (ENSG00000133818), RERG (ENSG00000134533), REM2 (ENSG00000139890), RIT1 (ENSG00000143622), RALB (ENSG00000144118), RIT2 (ENSG00000152214), MRAS (ENSG00000158186), DIRAS3 (ENSG00000162595), GEM (ENSG00000164949), DIRAS2 (ENSG00000165023), RRAD (ENSG00000166592), RHEBL1 (ENSG00000167550), NKIRAS2 (ENSG00000168256), HRAS (ENSG00000174775), DIRAS1 (ENSG00000176490), RAP2B (ENSG00000181467), ERAS (ENSG00000187682), NKIRAS1 (ENSG00000197885), NRAS (ENSG00000213281), RASL10B (ENSG00000270885)
Protein
Protein identifiers
Ras-like protein family member 10A — Q92737 (reviewed: Q92737)
Alternative names: Ras-like protein RRP22, Ras-related protein on chromosome 22
All UniProt accessions (1): Q92737
UniProt curated annotations — full annotation on UniProt →
Function. Potent inhibitor of cellular proliferation.
Subcellular location. Cell membrane. Nucleus. Nucleolus.
Tissue specificity. Expression appears to be strictly limited to the central nervous system.
Post-translational modifications. Isoprenylation is essential for nucleolar localization, and the proliferation-inhibiting activity of RASL10A.
Similarity. Belongs to the small GTPase superfamily. Ras family.
Isoforms (2)
| UniProt ID | Names | Canonical? |
|---|---|---|
| Q92737-1 | 1 | yes |
| Q92737-2 | 2, B |
RefSeq proteins (1): NP_006468* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR001806 | Small_GTPase | Family |
| IPR027417 | P-loop_NTPase | Homologous_superfamily |
| IPR052661 | Ras-like_GTPase_Reg | Family |
Pfam: PF00071
Catalyzed reactions (Rhea), 1 shown:
- GTP + H2O = GDP + phosphate + H(+) (RHEA:19669)
UniProt features (11 total): binding site 3, chain 1, propeptide 1, sequence conflict 1, region of interest 1, short sequence motif 1, modified residue 1, lipid moiety-binding region 1, splice variant 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q92737-F1 | 81.77 | 0.55 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Ligand- & substrate-binding residues (3): 11–18; 59–62; 129–132
Post-translational modifications (2): 200, 200
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 88 (showing top):
BENPORATH_ES_WITH_H3K27ME3, CAGCTG_AP4_Q5, MODULE_66, MODULE_157, MODULE_113, MODULE_242, MODULE_11, GOBP_SMALL_GTPASE_MEDIATED_SIGNAL_TRANSDUCTION, CAGCCTC_MIR4855P, IVANOVA_HEMATOPOIESIS_EARLY_PROGENITOR, MULLIGHAN_MLL_SIGNATURE_2_DN, MODULE_104, DOANE_BREAST_CANCER_CLASSES_UP, GOCC_NUCLEOLUS, GOMF_GTPASE_ACTIVITY
GO Biological Process (1): small GTPase-mediated signal transduction (GO:0007264)
GO Molecular Function (5): GTPase activity (GO:0003924), G protein activity (GO:0003925), GTP binding (GO:0005525), nucleotide binding (GO:0000166), hydrolase activity (GO:0016787)
GO Cellular Component (4): nucleolus (GO:0005730), plasma membrane (GO:0005886), nucleus (GO:0005634), membrane (GO:0016020)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| intracellular signaling cassette | 1 |
| ribonucleoside triphosphate phosphatase activity | 1 |
| GTPase activity | 1 |
| molecular function regulator activity | 1 |
| guanyl ribonucleotide binding | 1 |
| purine ribonucleoside triphosphate binding | 1 |
| nucleoside phosphate binding | 1 |
| heterocyclic compound binding | 1 |
| catalytic activity | 1 |
| nuclear lumen | 1 |
| intracellular membraneless organelle | 1 |
| membrane | 1 |
| cell periphery | 1 |
| intracellular membrane-bounded organelle | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
1279 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| RASL10A | GAS2L1 | Q99501 | 922 |
| RASL10A | AP1B1 | P78436 | 888 |
| RASL10A | GAS2L2 | Q8NHY3 | 812 |
| RASL10A | GAS2 | O43903 | 787 |
| RASL10A | SPA17 | Q15506 | 763 |
| RASL10A | EWSR1 | Q01844 | 751 |
| RASL10A | RASL12 | Q9NYN1 | 494 |
| RASL10A | RFPL1 | O75677 | 417 |
| RASL10A | AFTPH | Q6ULP2 | 341 |
| RASL10A | GLT8D2 | Q9H1C3 | 341 |
| RASL10A | ARFGAP3 | Q9NP61 | 314 |
| RASL10A | ZBTB8A | Q96BR9 | 313 |
| RASL10A | AGMAT | Q9BSE5 | 313 |
| RASL10A | ZMAT5 | Q9UDW3 | 307 |
| RASL10A | RER1 | O15258 | 305 |
IntAct
5 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| RASL10A | psi-mi:“MI:0915”(physical association) | 0.560 | |
| RASL10A | PRKRA | psi-mi:“MI:0914”(association) | 0.350 |
| RASL10A | psi-mi:“MI:0915”(physical association) | 0.000 |
BioGRID (16): RAP1GDS1 (Affinity Capture-MS), RAP1B (Affinity Capture-MS), RIC8B (Affinity Capture-MS), RHOA (Affinity Capture-MS), PRKRA (Affinity Capture-MS), RAP1GDS1 (Affinity Capture-MS), RHOA (Affinity Capture-MS), RAP1B (Affinity Capture-MS), PRKRA (Affinity Capture-MS), RASL10A (Synthetic Lethality), HOMEZ (Two-hybrid), PRKRA (Affinity Capture-MS), RAP1GDS1 (Affinity Capture-MS), RAP1B (Affinity Capture-MS), RHOA (Affinity Capture-MS)
ESM2 similar proteins: A1A5C7, A5D7B1, A6H7A0, A6NCF5, A6QLN9, A8MUP2, D3YYU8, D3ZZ80, O43688, O75147, O88843, P08887, Q14CX5, Q3SZQ2, Q3UHH2, Q58CT4, Q5EA19, Q5R4Q7, Q5R7S9, Q5RCI5, Q5RFN0, Q5SP67, Q5SUV1, Q642A6, Q6IA17, Q6PCB0, Q7TPB4, Q86TI4, Q8BGR6, Q8BZI6, Q8K5A4, Q8N5I2, Q8N653, Q8R2Z5, Q8TBF2, Q8VE98, Q92737, Q969P0, Q96NJ5, Q96NT3
Diamond homologs: A5A6J7, A6NIZ1, C4YKT4, E9R5S0, O35626, P01119, P0CY32, P11234, P13856, P18613, P22123, P22279, P36860, P52498, P61223, P61224, P62833, P62834, P62835, P62836, P79737, Q18246, Q19143, Q32NS2, Q4R379, Q4R9D4, Q4X241, Q550Q4, Q55BW0, Q59XU5, Q5R4B8, Q5RDM6, Q5ZHX1, Q5ZJW6, Q62636, Q640R7, Q6DGL2, Q6DGQ1, Q6IP71, Q6TEN1
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
27 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 27 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
699 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 22:29313857:CCCTA:C | donor_loss | 1.0000 |
| 22:29313862:C:CT | donor_loss | 1.0000 |
| 22:29313983:CACTC:C | acceptor_gain | 1.0000 |
| 22:29313985:CTC:C | acceptor_gain | 1.0000 |
| 22:29315029:T:TA | donor_gain | 1.0000 |
| 22:29313861:A:AC | donor_gain | 0.9900 |
| 22:29313862:C:CC | donor_gain | 0.9900 |
| 22:29313988:C:CC | acceptor_gain | 0.9900 |
| 22:29315003:C:A | donor_gain | 0.9900 |
| 22:29313986:TC:T | acceptor_gain | 0.9800 |
| 22:29313987:CC:C | acceptor_gain | 0.9800 |
| 22:29315013:T:A | donor_gain | 0.9800 |
| 22:29314980:ACACC:A | donor_gain | 0.9700 |
| 22:29314981:CACCC:C | donor_gain | 0.9700 |
| 22:29314990:CA:C | donor_gain | 0.9700 |
| 22:29315002:C:CA | donor_gain | 0.9700 |
| 22:29315023:GCTA:G | donor_loss | 0.9700 |
| 22:29315024:CTAC:C | donor_loss | 0.9700 |
| 22:29315026:A:C | donor_loss | 0.9700 |
| 22:29315027:C:CA | donor_loss | 0.9700 |
| 22:29313569:C:CC | acceptor_gain | 0.9600 |
| 22:29315029:TCCGG:T | donor_gain | 0.9600 |
| 22:29313564:CCGGC:C | acceptor_gain | 0.9500 |
| 22:29313565:CGGCC:C | acceptor_gain | 0.9500 |
| 22:29313569:CTGGG:C | acceptor_loss | 0.9500 |
| 22:29313570:T:A | acceptor_loss | 0.9500 |
| 22:29313577:C:T | acceptor_gain | 0.9500 |
| 22:29313984:ACTC:A | acceptor_gain | 0.9500 |
| 22:29313985:CTCC:C | acceptor_gain | 0.9500 |
| 22:29313986:TCCT:T | acceptor_gain | 0.9500 |
AlphaMissense
1291 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 22:29313523:C:A | K130N | 0.998 |
| 22:29313523:C:G | K130N | 0.998 |
| 22:29313526:G:C | N129K | 0.998 |
| 22:29313526:G:T | N129K | 0.998 |
| 22:29313907:A:C | S100R | 0.998 |
| 22:29313907:A:T | S100R | 0.998 |
| 22:29313909:T:G | S100R | 0.998 |
| 22:29313434:G:A | S160F | 0.997 |
| 22:29313926:T:A | D94V | 0.997 |
| 22:29313935:A:T | L91H | 0.997 |
| 22:29315077:A:T | I57N | 0.997 |
| 22:29313436:G:C | C159W | 0.996 |
| 22:29313525:T:C | K130E | 0.996 |
| 22:29313530:C:T | G128D | 0.996 |
| 22:29315077:A:G | I57T | 0.996 |
| 22:29315176:A:G | F24S | 0.996 |
| 22:29315197:T:A | K17M | 0.996 |
| 22:29315200:C:A | G16V | 0.996 |
| 22:29313431:G:T | A161D | 0.995 |
| 22:29313524:T:A | K130M | 0.995 |
| 22:29313932:A:T | V92D | 0.995 |
| 22:29313434:G:T | S160Y | 0.994 |
| 22:29313441:C:T | E158K | 0.994 |
| 22:29313457:C:A | W152C | 0.994 |
| 22:29313457:C:G | W152C | 0.994 |
| 22:29313930:A:C | Y93D | 0.994 |
| 22:29313938:A:T | V90E | 0.994 |
| 22:29315188:A:T | I20N | 0.994 |
| 22:29315200:C:T | G16D | 0.994 |
| 22:29315216:C:G | G11R | 0.994 |
dbSNP variants (sampled 300 via entrez): RS1000001882 (22:29318208 T>C,G), RS1000142819 (22:29315986 C>T), RS1000520114 (22:29318002 A>C), RS1000865897 (22:29316166 A>G), RS1001123125 (22:29316680 T>C), RS1001554584 (22:29316953 G>T), RS1001565668 (22:29313489 G>C,T), RS1002604041 (22:29314168 G>A), RS1002668764 (22:29315472 C>T), RS1003334607 (22:29314499 C>G,T), RS1003867283 (22:29321346 G>A), RS1003893016 (22:29319000 T>G), RS1003902260 (22:29314781 A>G), RS1003962936 (22:29314121 T>C), RS1003963416 (22:29321083 C>T)
Disease associations
OMIM: gene MIM:602220 | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
3 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST002553_2 | Pancreatic cancer | 1.000000e-08 |
| GCST004599_220 | Mean platelet volume | 3.000000e-12 |
| GCST90002395_618 | Mean platelet volume | 3.000000e-30 |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
17 total (human), top 17 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Arsenic Trioxide | decreases expression | 2 |
| Benzo(a)pyrene | increases methylation, increases expression | 2 |
| Valproic Acid | increases expression, affects expression | 2 |
| aristolochic acid I | increases expression | 1 |
| butyraldehyde | increases expression | 1 |
| abrine | increases expression | 1 |
| licochalcone B | increases expression | 1 |
| (+)-JQ1 compound | decreases expression | 1 |
| Decitabine | affects expression | 1 |
| Sunitinib | decreases expression | 1 |
| Acetaminophen | increases expression | 1 |
| Cisplatin | affects expression | 1 |
| Dinitrochlorobenzene | affects binding | 1 |
| Melphalan | increases expression | 1 |
| Smoke | decreases expression | 1 |
| Tretinoin | increases expression | 1 |
| Aflatoxin B1 | increases methylation | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): exocrine pancreatic carcinoma