RGPD4

gene
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Also known as RGP4DKFZp686P0288

Summary

RGPD4 (RANBP2 like and GRIP domain containing 4, HGNC:32417) is a protein-coding gene on chromosome 2q12.3, encoding RanBP2-like and GRIP domain-containing protein 4 (Q7Z3J3). It is a selective cancer dependency (DepMap: 16.4% of cell lines).

Predicted to contribute to GTPase activator activity. Predicted to be involved in NLS-bearing protein import into nucleus. Predicted to be part of nuclear pore. Predicted to be active in cytoplasm.

Source: NCBI Gene 285190 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 373 total
  • Cancer dependency (DepMap): dependent in 16.4% of screened cell lines
  • MANE Select transcript: NM_182588

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:32417
Approved symbolRGPD4
NameRANBP2 like and GRIP domain containing 4
Location2q12.3
Locus typegene with protein product
StatusApproved
AliasesRGP4, DKFZp686P0288
Ensembl geneENSG00000196862
Ensembl biotypeprotein_coding
OMIM612707
Entrez285190

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000408999

RefSeq mRNA: 1 — MANE Select: NM_182588 NM_182588

CCDS: CCDS46381

Canonical transcript exons

ENST00000408999 — 23 exons

ExonStartEnd
ENSE00001872929107826892107827085
ENSE00001910458107890721107892544
ENSE00002445986107861194107861331
ENSE00002452314107862949107863032
ENSE00002455397107869883107869977
ENSE00002457670107859722107859845
ENSE00002464767107843009107843239
ENSE00002471423107838812107838964
ENSE00002478426107843585107843730
ENSE00002483308107861594107861740
ENSE00002483655107882672107882873
ENSE00002483815107854556107854643
ENSE00002486568107866190107866325
ENSE00002495853107836602107836669
ENSE00002500115107862682107862861
ENSE00002505121107838257107838368
ENSE00002514284107879968107880107
ENSE00002520911107859114107859295
ENSE00002524501107870705107872928
ENSE00002525608107859379107859554
ENSE00002526803107860766107860927
ENSE00002527577107856760107856969
ENSE00002530598107848341107848536

Expression profiles

Bgee: expression breadth ubiquitous, 120 present calls, max score 76.70.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047376.70gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099175.24gold quality
testisUBERON:000047362.13gold quality
left testisUBERON:000453361.38gold quality
right testisUBERON:000453461.06gold quality
mucosa of transverse colonUBERON:000499159.85gold quality
ventricular zoneUBERON:000305357.98gold quality
primary visual cortexUBERON:000243656.96gold quality
hindlimb stylopod muscleUBERON:000425256.24gold quality
islet of LangerhansUBERON:000000654.64gold quality
superior frontal gyrusUBERON:000266154.17gold quality
ganglionic eminenceUBERON:000402353.04silver quality
granulocyteCL:000009452.29gold quality
endometriumUBERON:000129551.05gold quality
urinary bladderUBERON:000125550.86gold quality
pancreasUBERON:000126450.55gold quality
right lobe of liverUBERON:000111450.43gold quality
tibial arteryUBERON:000761050.24gold quality
popliteal arteryUBERON:000225050.23gold quality
colonic epitheliumUBERON:000039750.09gold quality
putamenUBERON:000187450.08gold quality
muscle of legUBERON:000138349.95gold quality
gastrocnemiusUBERON:000138849.90gold quality
anterior cingulate cortexUBERON:000983549.78gold quality
Brodmann (1909) area 9UBERON:001354049.27gold quality
dorsolateral prefrontal cortexUBERON:000983449.23gold quality
liverUBERON:000210749.18silver quality
lower esophagus mucosaUBERON:003583449.11gold quality
left adrenal gland cortexUBERON:003582549.09gold quality
body of pancreasUBERON:000115048.98gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.00

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

113 targeting RGPD4, 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-513A-5P100.0069.772465
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-12118100.0065.881270
HSA-MIR-450A-1-3P100.0069.331837
HSA-MIR-340-5P100.0072.504437
HSA-MIR-126-5P100.0072.713180
HSA-MIR-4262100.0073.263931
HSA-MIR-4425100.0067.591049
HSA-MIR-548AW99.9972.573559
HSA-MIR-186-5P99.9970.833707
HSA-MIR-181A-5P99.9972.962995
HSA-MIR-181B-5P99.9972.972996
HSA-MIR-181C-5P99.9972.952996
HSA-MIR-181D-5P99.9973.042997
HSA-MIR-118499.9968.191458
HSA-MIR-27A-3P99.9872.132955
HSA-MIR-27B-3P99.9872.132955
HSA-MIR-998599.9872.112939
HSA-MIR-103A-3P99.9869.141595
HSA-MIR-10799.9869.141595
HSA-MIR-6891-5P99.9866.531372
HSA-MIR-3173-3P99.9866.491217
HSA-LET-7F-2-3P99.9870.982588
HSA-MIR-1185-1-3P99.9871.042593
HSA-MIR-1185-2-3P99.9871.042593
HSA-MIR-485-3P99.9870.681585
HSA-MIR-539-3P99.9870.741616
HSA-MIR-1213699.9872.815713
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-426799.9666.532368

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 16.4% of screened cell lines.

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
danio_rerioranbp3aENSDARG00000008727
drosophila_melanogasterRanBP3FBGN0039110

Paralogs (10): RGPD5 (ENSG00000015568), RANBP3 (ENSG00000031823), RANBP1 (ENSG00000099901), RGPD3 (ENSG00000153165), RANBP2 (ENSG00000153201), RANBP3L (ENSG00000164188), RGPD8 (ENSG00000169629), RGPD6 (ENSG00000183054), RGPD2 (ENSG00000185304), RGPD1 (ENSG00000187627)

Protein

Protein identifiers

RanBP2-like and GRIP domain-containing protein 4Q7Z3J3 (reviewed: Q7Z3J3)

All UniProt accessions (1): Q7Z3J3

UniProt curated annotations — full annotation on UniProt →

Miscellaneous. One of the 8 copies of RANBP2 clustered close to the chromosome 2 centromere.

Isoforms (2)

UniProt IDNamesCanonical?
Q7Z3J3-11yes
Q7Z3J3-22

RefSeq proteins (1): NP_872394* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000156Ran_bind_domDomain
IPR000237GRIP_domDomain
IPR011990TPR-like_helical_dom_sfHomologous_superfamily
IPR011993PH-like_dom_sfHomologous_superfamily
IPR019734TPR_rptRepeat
IPR032023GCC2_Rab_bindDomain
IPR045255RanBP1-likeFamily

Pfam: PF00638, PF01465, PF13181, PF16704

UniProt features (19 total): compositionally biased region 6, region of interest 4, domain 3, repeat 2, splice variant 2, chain 1, modified residue 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q7Z3J3-F167.370.27

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (1): 21

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 55 (showing top): GOBP_INTRACELLULAR_PROTEIN_TRANSPORT, chr2q12, GOBP_ESTABLISHMENT_OF_PROTEIN_LOCALIZATION_TO_ORGANELLE, GOBP_NUCLEAR_TRANSPORT, MARZEC_IL2_SIGNALING_DN, GOBP_PROTEIN_LOCALIZATION_TO_ORGANELLE, GOBP_NLS_BEARING_PROTEIN_IMPORT_INTO_NUCLEUS, GOBP_NUCLEAR_EXPORT, GRYDER_PAX3FOXO1_ENHANCERS_IN_TADS, GOBP_PROTEIN_LOCALIZATION_TO_NUCLEUS, GOCC_NUCLEAR_ENVELOPE, GOCC_NUCLEAR_PORE, GOMF_ACYLTRANSFERASE_ACTIVITY, GOMF_SUMO_TRANSFERASE_ACTIVITY, GOMF_AMINOACYLTRANSFERASE_ACTIVITY

GO Biological Process (2): NLS-bearing protein import into nucleus (GO:0006607), intracellular transport (GO:0046907)

GO Molecular Function (2): GTPase activator activity (GO:0005096), protein binding (GO:0005515)

GO Cellular Component (2): nuclear pore (GO:0005643), cytoplasm (GO:0005737)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
intracellular anatomical structure2
protein import into nucleus1
transport1
cellular localization1
establishment of localization in cell1
GTPase activity1
enzyme activator activity1
GTPase regulator activity1
binding1
nuclear envelope1
nuclear protein-containing complex1
cellular anatomical structure1

Protein interactions and networks

STRING

1636 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
RGPD4GRIP1Q9Y3R0706
RGPD4USP17L13C9JLJ4570
RGPD4SUMO1P55856471
RGPD4C16orf90A8MZG2440
RGPD4WFDC11Q8NEX6436
RGPD4IQCF3P0C7M6413
RGPD4SPANXN5Q5MJ07405
RGPD4AADACL2Q6P093395
RGPD4TXNDC8Q6A555369
RGPD4DEFB112Q30KQ8368
RGPD4GCC2Q8IWJ2366
RGPD4POTEHQ6S545355
RGPD4SH3TC1Q8TE82349
RGPD4CIB4A0PJX0338
RGPD4SIRAL2Q9NWS6326

IntAct

9 interactions, top by confidence:

ABTypeScore
CFTRESYT2psi-mi:“MI:0914”(association)0.710
RANRGPD8psi-mi:“MI:0914”(association)0.640
PLK1ERCC6Lpsi-mi:“MI:0914”(association)0.350
UVRAGDFFApsi-mi:“MI:0914”(association)0.350
KPNA4POM121Cpsi-mi:“MI:0914”(association)0.350
NUMA1SHANK3psi-mi:“MI:0914”(association)0.350
RANNUP214psi-mi:“MI:0914”(association)0.350
CIB2APAF1psi-mi:“MI:0914”(association)0.350

BioGRID (24): RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Affinity Capture-MS), RGPD4 (Proximity Label-MS), RGPD4 (Affinity Capture-MS), RGPD5 (Cross-Linking-MS (XL-MS)), RGPD4 (Cross-Linking-MS (XL-MS)), RGPD4 (Cross-Linking-MS (XL-MS))

ESM2 similar proteins: A0A0B4K7J2, A1ZAK1, A6NKT7, F4J8D3, G5ED39, H2QII6, O01510, O14715, O48767, P0DJD0, P0DJD1, P12798, P33144, P40358, P42286, P49792, Q00416, Q0IEK6, Q18508, Q18892, Q20937, Q291E4, Q2U639, Q4WVM7, Q5B8K7, Q61CW2, Q61WP7, Q6C9G0, Q6CXL5, Q6FUS3, Q6FVG5, Q70PP2, Q751J3, Q754V0, Q759B7, Q759Y1, Q75B70, Q75CM2, Q7TSH2, Q7Z3J3

Diamond homologs: A0A0B4K7J2, A6NKT7, E9Q3G8, H2QII6, O14715, P0DJD0, P0DJD1, P34022, P40517, P41920, P43487, P92985, Q09717, Q3T0M7, Q54KD9, Q7Z3J3, Q8RWG8, Q99666, Q9C829, Q9LMK7, Q9USL4, D3ZZL9, P32499, P34562, P48820, P49792, Q8CHG3, Q8IWJ2, Q9ERU9, G0S8I1, Q09146, Q86VV4, A0A075B759, A0A075B767, A0A0B4J2A2, A0A0R0H9T5, A4FV72, D4AY02, F5H284, O00060

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

373 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance328
Likely benign38
Benign2

Top pathogenic / likely-pathogenic (0)

SpliceAI

3082 predictions. Top by Δscore:

VariantEffectΔscore
2:107836596:TTTTA:Tacceptor_loss1.0000
2:107836597:TTTAG:Tacceptor_loss1.0000
2:107836599:TA:Tacceptor_loss1.0000
2:107836600:A:AGacceptor_gain1.0000
2:107836600:A:Tacceptor_loss1.0000
2:107836601:G:GTacceptor_gain1.0000
2:107836601:GA:Gacceptor_gain1.0000
2:107836601:GAA:Gacceptor_gain1.0000
2:107836601:GAAGT:Gacceptor_gain1.0000
2:107836665:AAAAA:Adonor_gain1.0000
2:107836666:AAAA:Adonor_gain1.0000
2:107836666:AAAAG:Adonor_loss1.0000
2:107836667:AAA:Adonor_gain1.0000
2:107836667:AAAGT:Adonor_loss1.0000
2:107836668:AA:Adonor_gain1.0000
2:107836668:AAGT:Adonor_loss1.0000
2:107836669:AG:Adonor_loss1.0000
2:107836670:G:GGdonor_gain1.0000
2:107836670:G:Tdonor_loss1.0000
2:107836671:TAA:Tdonor_loss1.0000
2:107838248:A:AGacceptor_gain1.0000
2:107838249:A:Gacceptor_gain1.0000
2:107838255:A:AGacceptor_gain1.0000
2:107838256:G:GGacceptor_gain1.0000
2:107838256:GATAC:Gacceptor_gain1.0000
2:107838365:CAGGG:Cdonor_loss1.0000
2:107838366:AGGGT:Adonor_loss1.0000
2:107838367:GG:Gdonor_gain1.0000
2:107838368:GG:Gdonor_gain1.0000
2:107838369:G:GAdonor_loss1.0000

AlphaMissense

11578 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
2:107859822:T:AW579R0.995
2:107859822:T:CW579R0.995
2:107859155:T:AW440R0.994
2:107859155:T:CW440R0.994
2:107859517:T:AW533R0.994
2:107859517:T:CW533R0.994
2:107859754:T:AV556D0.994
2:107860814:A:CS603R0.994
2:107860816:T:AS603R0.994
2:107860816:T:GS603R0.994
2:107859514:T:AW532R0.993
2:107859514:T:CW532R0.993
2:107861324:T:CL684P0.992
2:107854634:A:CS353R0.991
2:107854636:C:AS353R0.991
2:107854636:C:GS353R0.991
2:107859287:G:CD484H0.991
2:107859291:T:CL485P0.991
2:107859386:T:CL489P0.991
2:107859391:G:AG491R0.991
2:107859391:G:CG491R0.991
2:107859835:T:CL583P0.991
2:107861691:T:CL719P0.991
2:107859210:T:CL458P0.990
2:107859276:T:AI480K0.990
2:107860813:A:CR602S0.990
2:107860813:A:TR602S0.990
2:107859288:A:CD484A0.989
2:107843210:T:AW203R0.988
2:107843210:T:CW203R0.988

dbSNP variants (sampled 300 via entrez): RS1000017831 (2:107836132 G>A), RS1000018256 (2:107855354 C>T), RS1000149172 (2:107845544 G>A,C,T), RS1000194393 (2:107887923 T>A,C), RS1000203318 (2:107845123 C>T), RS1000453093 (2:107855537 C>T), RS1000476870 (2:107831670 G>A,T), RS1000600839 (2:107825016 T>C), RS1000607198 (2:107884582 T>A,G), RS1000733399 (2:107878506 A>G), RS1000804820 (2:107879656 G>A), RS1000849302 (2:107832049 T>C), RS1000879929 (2:107861934 G>A,T), RS1001039938 (2:107884877 G>A), RS1001053886 (2:107854049 C>G)

Disease associations

OMIM: gene MIM:612707 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

4 total (human), top 4 by PubMed support.

ChemicalActions (top 5)PubMed papers
Resveratrolincreases expression, affects cotreatment1
Plant Extractsaffects cotreatment, increases expression1
Valproic Aciddecreases methylation1
Aflatoxin B1decreases methylation1

Clinical trials (associated diseases)

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

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.