RASL10A

gene
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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

FieldValue
HGNC IDHGNC:16954
Approved symbolRASL10A
NameRAS like family 10 member A
Location22q12.2
Locus typegene with protein product
StatusApproved
AliasesRRP22
Ensembl geneENSG00000100276
Ensembl biotypeprotein_coding
OMIM602220
Entrez10633

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

ExonStartEnd
ENSE000006520402931386329313987
ENSE000008797332931502829315697
ENSE000013261052931293329313568

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 IDTPM avgSamples expressed
1935180.7043254
1935170.297877
1935190.156584
1935150.042028
1935160.021816

Top tissues by expression

288 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
amygdalaUBERON:000187689.54gold quality
middle temporal gyrusUBERON:000277188.16gold quality
Brodmann (1909) area 9UBERON:001354088.02gold quality
right frontal lobeUBERON:000281087.66gold quality
cingulate cortexUBERON:000302787.23gold quality
dorsolateral prefrontal cortexUBERON:000983487.11gold quality
anterior cingulate cortexUBERON:000983587.06gold quality
temporal lobeUBERON:000187187.02gold quality
cortical plateUBERON:000534386.54gold quality
prefrontal cortexUBERON:000045185.77gold quality
frontal cortexUBERON:000187084.86gold quality
neocortexUBERON:000195084.81gold quality
nucleus accumbensUBERON:000188284.65gold quality
cerebral cortexUBERON:000095684.35gold quality
caudate nucleusUBERON:000187384.26gold quality
entorhinal cortexUBERON:000272884.22gold quality
Brodmann (1909) area 46UBERON:000648383.92gold quality
telencephalonUBERON:000189383.80gold quality
orbitofrontal cortexUBERON:000416783.79gold quality
putamenUBERON:000187483.39gold quality
Ammon’s hornUBERON:000195483.02gold quality
forebrainUBERON:000189082.88gold quality
superior frontal gyrusUBERON:000266182.18gold quality
primary visual cortexUBERON:000243682.06gold quality
Brodmann (1909) area 10UBERON:001354181.84silver quality
hypothalamusUBERON:000189881.82gold quality
endothelial cellCL:000011581.31silver quality
CA1 field of hippocampusUBERON:000388180.89gold quality
brainUBERON:000095580.75gold quality
central nervous systemUBERON:000101780.50gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no1.88

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):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-186-5P99.9970.833707
HSA-MIR-204-5P99.7971.622439
HSA-MIR-211-5P99.7971.652440
HSA-MIR-4446-5P99.7269.192544
HSA-MIR-4755-5P99.7170.342716
HSA-MIR-5006-3P99.7170.262728
HSA-MIR-608699.7065.38699
HSA-MIR-6832-3P99.5270.441726
HSA-MIR-3688-5P99.1269.671091
HSA-MIR-891A-3P98.0567.99970
HSA-MIR-607298.0066.47804
HSA-MIR-6762-5P96.5564.62972
HSA-MIR-6845-5P96.5564.65969
HSA-MIR-797396.4865.54502
HSA-MIR-644A96.0266.52786
HSA-MIR-6891-3P95.8065.76683
HSA-MIR-6874-5P95.7364.94545
HSA-MIR-1247-5P85.9261.0765

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

OrganismSymbolGene ID
mus_musculusRasl10aENSMUSG00000034209
rattus_norvegicusRasl10aENSRNOG00000008951

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 10AQ92737 (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 IDNamesCanonical?
Q92737-11yes
Q92737-22, B

RefSeq proteins (1): NP_006468* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001806Small_GTPaseFamily
IPR027417P-loop_NTPaseHomologous_superfamily
IPR052661Ras-like_GTPase_RegFamily

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)

ModelpLDDTFraction very-high
AF-Q92737-F181.770.55

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:

CategoryTerms
intracellular signaling cassette1
ribonucleoside triphosphate phosphatase activity1
GTPase activity1
molecular function regulator activity1
guanyl ribonucleotide binding1
purine ribonucleoside triphosphate binding1
nucleoside phosphate binding1
heterocyclic compound binding1
catalytic activity1
nuclear lumen1
intracellular membraneless organelle1
membrane1
cell periphery1
intracellular membrane-bounded organelle1
cellular anatomical structure1

Protein interactions and networks

STRING

1279 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
RASL10AGAS2L1Q99501922
RASL10AAP1B1P78436888
RASL10AGAS2L2Q8NHY3812
RASL10AGAS2O43903787
RASL10ASPA17Q15506763
RASL10AEWSR1Q01844751
RASL10ARASL12Q9NYN1494
RASL10ARFPL1O75677417
RASL10AAFTPHQ6ULP2341
RASL10AGLT8D2Q9H1C3341
RASL10AARFGAP3Q9NP61314
RASL10AZBTB8AQ96BR9313
RASL10AAGMATQ9BSE5313
RASL10AZMAT5Q9UDW3307
RASL10ARER1O15258305

IntAct

5 interactions, top by confidence:

ABTypeScore
RASL10Apsi-mi:“MI:0915”(physical association)0.560
RASL10APRKRApsi-mi:“MI:0914”(association)0.350
RASL10Apsi-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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance27
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

699 predictions. Top by Δscore:

VariantEffectΔscore
22:29313857:CCCTA:Cdonor_loss1.0000
22:29313862:C:CTdonor_loss1.0000
22:29313983:CACTC:Cacceptor_gain1.0000
22:29313985:CTC:Cacceptor_gain1.0000
22:29315029:T:TAdonor_gain1.0000
22:29313861:A:ACdonor_gain0.9900
22:29313862:C:CCdonor_gain0.9900
22:29313988:C:CCacceptor_gain0.9900
22:29315003:C:Adonor_gain0.9900
22:29313986:TC:Tacceptor_gain0.9800
22:29313987:CC:Cacceptor_gain0.9800
22:29315013:T:Adonor_gain0.9800
22:29314980:ACACC:Adonor_gain0.9700
22:29314981:CACCC:Cdonor_gain0.9700
22:29314990:CA:Cdonor_gain0.9700
22:29315002:C:CAdonor_gain0.9700
22:29315023:GCTA:Gdonor_loss0.9700
22:29315024:CTAC:Cdonor_loss0.9700
22:29315026:A:Cdonor_loss0.9700
22:29315027:C:CAdonor_loss0.9700
22:29313569:C:CCacceptor_gain0.9600
22:29315029:TCCGG:Tdonor_gain0.9600
22:29313564:CCGGC:Cacceptor_gain0.9500
22:29313565:CGGCC:Cacceptor_gain0.9500
22:29313569:CTGGG:Cacceptor_loss0.9500
22:29313570:T:Aacceptor_loss0.9500
22:29313577:C:Tacceptor_gain0.9500
22:29313984:ACTC:Aacceptor_gain0.9500
22:29313985:CTCC:Cacceptor_gain0.9500
22:29313986:TCCT:Tacceptor_gain0.9500

AlphaMissense

1291 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
22:29313523:C:AK130N0.998
22:29313523:C:GK130N0.998
22:29313526:G:CN129K0.998
22:29313526:G:TN129K0.998
22:29313907:A:CS100R0.998
22:29313907:A:TS100R0.998
22:29313909:T:GS100R0.998
22:29313434:G:AS160F0.997
22:29313926:T:AD94V0.997
22:29313935:A:TL91H0.997
22:29315077:A:TI57N0.997
22:29313436:G:CC159W0.996
22:29313525:T:CK130E0.996
22:29313530:C:TG128D0.996
22:29315077:A:GI57T0.996
22:29315176:A:GF24S0.996
22:29315197:T:AK17M0.996
22:29315200:C:AG16V0.996
22:29313431:G:TA161D0.995
22:29313524:T:AK130M0.995
22:29313932:A:TV92D0.995
22:29313434:G:TS160Y0.994
22:29313441:C:TE158K0.994
22:29313457:C:AW152C0.994
22:29313457:C:GW152C0.994
22:29313930:A:CY93D0.994
22:29313938:A:TV90E0.994
22:29315188:A:TI20N0.994
22:29315200:C:TG16D0.994
22:29315216:C:GG11R0.994

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):

StudyTraitp-value
GCST002553_2Pancreatic cancer1.000000e-08
GCST004599_220Mean platelet volume3.000000e-12
GCST90002395_618Mean platelet volume3.000000e-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.

ChemicalActions (top 5)PubMed papers
Arsenic Trioxidedecreases expression2
Benzo(a)pyreneincreases methylation, increases expression2
Valproic Acidincreases expression, affects expression2
aristolochic acid Iincreases expression1
butyraldehydeincreases expression1
abrineincreases expression1
licochalcone Bincreases expression1
(+)-JQ1 compounddecreases expression1
Decitabineaffects expression1
Sunitinibdecreases expression1
Acetaminophenincreases expression1
Cisplatinaffects expression1
Dinitrochlorobenzeneaffects binding1
Melphalanincreases expression1
Smokedecreases expression1
Tretinoinincreases expression1
Aflatoxin B1increases methylation1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): exocrine pancreatic carcinoma