RAB19
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Also known as RAB19B
Summary
RAB19 (RAB19, member RAS oncogene family, HGNC:19982) is a protein-coding gene on chromosome 7q34, encoding Ras-related protein Rab-19 (A4D1S5). The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes.
Predicted to enable GTPase activity. Predicted to be involved in autophagosome assembly and intracellular protein transport. Located in extracellular exosome.
Source: NCBI Gene 401409 — RefSeq curated summary.
At a glance
- GWAS associations: 1
- Clinical variants (ClinVar): 52 total
- MANE Select transcript:
NM_001008749
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:19982 |
| Approved symbol | RAB19 |
| Name | RAB19, member RAS oncogene family |
| Location | 7q34 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | RAB19B |
| Ensembl gene | ENSG00000146955 |
| Ensembl biotype | protein_coding |
| Entrez | 401409 |
Gene structure
Transcript identifiers
Ensembl transcripts: 8 — 8 protein_coding
ENST00000356407, ENST00000537763, ENST00000897794, ENST00000897795, ENST00000897796, ENST00000897797, ENST00000924028, ENST00000924029
RefSeq mRNA: 1 — MANE Select: NM_001008749
NM_001008749
CCDS: CCDS34762
Canonical transcript exons
ENST00000537763 — 4 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001805995 | 140411874 | 140412057 |
| ENSE00001843508 | 140404058 | 140404217 |
| ENSE00001884985 | 140425882 | 140427974 |
| ENSE00001956705 | 140407624 | 140407847 |
Expression profiles
Bgee: expression breadth broad, 73 present calls, max score 73.50.
FANTOM5 (CAGE): breadth broad, TPM avg 0.6418 / max 17.4386, expressed in 267 samples.
FANTOM5 promoters (2 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 81505 | 0.3752 | 202 |
| 81506 | 0.2666 | 172 |
Top tissues by expression
118 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| mucosa of transverse colon | UBERON:0004991 | 73.50 | gold quality |
| bone marrow cell | CL:0002092 | 70.73 | gold quality |
| bone marrow | UBERON:0002371 | 69.87 | gold quality |
| islet of Langerhans | UBERON:0000006 | 69.74 | gold quality |
| rectum | UBERON:0001052 | 67.96 | gold quality |
| pancreas | UBERON:0001264 | 67.49 | gold quality |
| duodenum | UBERON:0002114 | 66.58 | gold quality |
| body of pancreas | UBERON:0001150 | 66.01 | gold quality |
| metanephros cortex | UBERON:0010533 | 65.14 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 64.51 | gold quality |
| blood | UBERON:0000178 | 63.47 | gold quality |
| kidney | UBERON:0002113 | 63.18 | gold quality |
| cortex of kidney | UBERON:0001225 | 61.98 | gold quality |
| colonic epithelium | UBERON:0000397 | 61.11 | silver quality |
| right lobe of thyroid gland | UBERON:0001119 | 60.82 | gold quality |
| pituitary gland | UBERON:0000007 | 59.81 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 59.67 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 58.88 | gold quality |
| thyroid gland | UBERON:0002046 | 58.78 | gold quality |
| tonsil | UBERON:0002372 | 58.66 | gold quality |
| transverse colon | UBERON:0001157 | 58.42 | gold quality |
| lymph node | UBERON:0000029 | 58.39 | gold quality |
| adenohypophysis | UBERON:0002196 | 57.84 | gold quality |
| vermiform appendix | UBERON:0001154 | 57.77 | gold quality |
| placenta | UBERON:0001987 | 56.60 | gold quality |
| granulocyte | CL:0000094 | 56.52 | gold quality |
| gall bladder | UBERON:0002110 | 55.47 | gold quality |
| small intestine | UBERON:0002108 | 54.63 | gold quality |
| small intestine Peyer’s patch | UBERON:0003454 | 53.58 | gold quality |
| stomach | UBERON:0000945 | 52.08 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.79 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
6 targeting RAB19, 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-9-5P | 100.00 | 72.28 | 2361 |
| HSA-MIR-29B-2-5P | 99.67 | 68.98 | 1726 |
| HSA-MIR-6744-3P | 99.22 | 64.41 | 972 |
| HSA-MIR-4757-5P | 99.12 | 64.51 | 981 |
| HSA-MIR-6781-3P | 97.44 | 66.85 | 970 |
| HSA-MIR-2682-3P | 97.10 | 66.16 | 840 |
Literature-anchored findings (GeneRIF, showing 2)
- N6-methyladenosine (m6A)-mediated up-regulation of long noncoding RNA LINC01320 promotes the proliferation, migration, and invasion of gastric cancer via miR495-5p/RAB19 axis. (PMID:34288797)
- WDR38, a novel equatorial segment protein, interacts with the GTPase protein RAB19 and Golgi protein GM130 to play roles in acrosome biogenesis. (PMID:37635409)
Cross-species orthologs
4 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| ENSDARG00000099205 | ||
| danio_rerio | RAB19 | ENSDARG00000101150 |
| mus_musculus | Rab19 | ENSMUSG00000029923 |
| rattus_norvegicus | Rab19 | ENSRNOG00000009030 |
Paralogs (68): RAB27B (ENSG00000041353), RAB27A (ENSG00000069974), RAB7A (ENSG00000075785), RABL2B (ENSG00000079974), RAB21 (ENSG00000080371), RAB10 (ENSG00000084733), RAB18 (ENSG00000099246), RAB36 (ENSG00000100228), IFT27 (ENSG00000100360), RAB40AL (ENSG00000102128), RAB11A (ENSG00000103769), RAB2A (ENSG00000104388), RAB3D (ENSG00000105514), RAB3A (ENSG00000105649), RAB5C (ENSG00000108774), RAB34 (ENSG00000109113), RAB5B (ENSG00000111540), RAB35 (ENSG00000111737), RAB23 (ENSG00000112210), DNAJC27 (ENSG00000115137), RAB29 (ENSG00000117280), RAB32 (ENSG00000118508), RAB14 (ENSG00000119396), RAB9B (ENSG00000123570), RAB9A (ENSG00000123595), RAB38 (ENSG00000123892), RAB22A (ENSG00000124209), RAB17 (ENSG00000124839), RAB2B (ENSG00000129472), RAB25 (ENSG00000132698), RAB33A (ENSG00000134594), RAB30 (ENSG00000137502), RAB1A (ENSG00000138069), RAB20 (ENSG00000139832), RAB15 (ENSG00000139998), RAB40B (ENSG00000141542), RAB13 (ENSG00000143545), RABL2A (ENSG00000144134), RAB5A (ENSG00000144566), RAB41 (ENSG00000147127)
Protein
Protein identifiers
Ras-related protein Rab-19 — A4D1S5 (reviewed: A4D1S5)
All UniProt accessions (1): A4D1S5
UniProt curated annotations — full annotation on UniProt →
Function. The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes. Rabs cycle between an inactive GDP-bound form and an active GTP-bound form that is able to recruit to membranes different set of downstream effectors directly responsible for vesicle formation, movement, tethering and fusion.
Subcellular location. Cell membrane.
Activity regulation. Regulated by guanine nucleotide exchange factors (GEFs) which promote the exchange of bound GDP for free GTP. Regulated by GTPase activating proteins (GAPs) which increase the GTP hydrolysis activity. Inhibited by GDP dissociation inhibitors (GDIs).
Domain organisation. Switch 1, switch 2 and the interswitch regions are characteristic of Rab GTPases and mediate the interactions with Rab downstream effectors. The switch regions undergo conformational changes upon nucleotide binding which drives interaction with specific sets of effector proteins, with most effectors only binding to GTP-bound Rab.
Similarity. Belongs to the small GTPase superfamily. Rab family.
Isoforms (2)
| UniProt ID | Names | Canonical? |
|---|---|---|
| A4D1S5-1 | 1 | yes |
| A4D1S5-2 | 2 |
RefSeq proteins (1): NP_001008749* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR001806 | Small_GTPase | Family |
| IPR005225 | Small_GTP-bd | Domain |
| IPR027417 | P-loop_NTPase | Homologous_superfamily |
| IPR048040 | Rab19/43 | Family |
| IPR050209 | Rab_GTPases_membrane_traffic | Family |
Pfam: PF00071
Catalyzed reactions (Rhea), 1 shown:
- GTP + H2O = GDP + phosphate + H(+) (RHEA:19669)
UniProt features (29 total): binding site 21, short sequence motif 2, lipid moiety-binding region 2, chain 1, modified residue 1, splice variant 1, sequence conflict 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A4D1S5-F1 | 83.68 | 0.66 |
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 (21): 42; 43; 44; 45; 49; 49; 72; 75; 130; 131; 133; 161 …
Post-translational modifications (3): 217, 215, 217
Function
Pathways and Gene Ontology
Reactome pathways
1 pathways
| ID | Pathway |
|---|---|
| R-HSA-8873719 | RAB geranylgeranylation |
MSigDB gene sets: 93 (showing top):
GSE45365_NK_CELL_VS_BCELL_DN, GOBP_VACUOLE_ORGANIZATION, GOBP_INTRACELLULAR_PROTEIN_TRANSPORT, GOBP_MACROAUTOPHAGY, GOBP_ORGANELLE_ASSEMBLY, GOBP_AUTOPHAGOSOME_ORGANIZATION, ZHENG_BOUND_BY_FOXP3, MARSON_BOUND_BY_FOXP3_STIMULATED, MARSON_BOUND_BY_FOXP3_UNSTIMULATED, GOMF_GTPASE_ACTIVITY, GOMF_HYDROLASE_ACTIVITY_ACTING_ON_ACID_ANHYDRIDES, CHEN_METABOLIC_SYNDROM_NETWORK, REACTOME_POST_TRANSLATIONAL_PROTEIN_MODIFICATION, MIKKELSEN_ES_ICP_WITH_H3K4ME3, LI_INDUCED_T_TO_NATURAL_KILLER_UP
GO Biological Process (2): autophagosome assembly (GO:0000045), intracellular protein transport (GO:0006886)
GO Molecular Function (7): GTPase activity (GO:0003924), G protein activity (GO:0003925), GTP binding (GO:0005525), metal ion binding (GO:0046872), nucleotide binding (GO:0000166), protein binding (GO:0005515), hydrolase activity (GO:0016787)
GO Cellular Component (4): plasma membrane (GO:0005886), endomembrane system (GO:0012505), extracellular exosome (GO:0070062), membrane (GO:0016020)
Reactome top-level categories
Rollup of top-1 pathways:
| Category | Pathways |
|---|---|
| Post-translational protein modification | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| cellular anatomical structure | 2 |
| Atg12 activating enzyme activity | 1 |
| protein-phosphatidylethanolamide deconjugating activity | 1 |
| Atg12 conjugating enzyme activity | 1 |
| Atg12 ligase activity | 1 |
| organelle assembly | 1 |
| Atg1/ULK1 kinase complex assembly | 1 |
| autophagosome organization | 1 |
| intracellular protein localization | 1 |
| protein transport | 1 |
| intracellular transport | 1 |
| ribonucleoside triphosphate phosphatase activity | 1 |
| GTPase activity | 1 |
| molecular function regulator activity | 1 |
| guanyl ribonucleotide binding | 1 |
| purine ribonucleoside triphosphate binding | 1 |
| cation binding | 1 |
| nucleoside phosphate binding | 1 |
| heterocyclic compound binding | 1 |
| binding | 1 |
| catalytic activity | 1 |
| membrane | 1 |
| cell periphery | 1 |
| vacuole | 1 |
| plasma membrane | 1 |
| extracellular vesicle | 1 |
Protein interactions and networks
STRING
1279 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| RAB19 | GOLGA1 | Q92805 | 572 |
| RAB19 | RAB18 | Q9NP72 | 519 |
| RAB19 | TBC1D4 | O60343 | 490 |
| RAB19 | ARMH1 | Q6PIY5 | 489 |
| RAB19 | RAB6A | P20340 | 485 |
| RAB19 | RAB30 | Q15771 | 469 |
| RAB19 | RAB2A | P08886 | 450 |
| RAB19 | RAB11A | P24410 | 426 |
| RAB19 | RAB4A | P20338 | 423 |
| RAB19 | RAB39A | Q14964 | 415 |
| RAB19 | FAM162B | Q5T6X4 | 397 |
| RAB19 | F2RL2 | O00254 | 387 |
| RAB19 | STX6 | O43752 | 380 |
| RAB19 | TRAPPC1 | Q9Y5R8 | 348 |
| RAB19 | COL6A5 | A8TX70 | 338 |
IntAct
19 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| RAB19 | KRTAP10-8 | psi-mi:“MI:0915”(physical association) | 0.560 |
| RAB19 | RABIF | psi-mi:“MI:0915”(physical association) | 0.560 |
| VCAN | RAB19 | psi-mi:“MI:0915”(physical association) | 0.560 |
| RAB19 | LSM11 | psi-mi:“MI:0915”(physical association) | 0.560 |
| RAB10 | RAB19 | psi-mi:“MI:0914”(association) | 0.350 |
| GOLM1 | RAB19 | psi-mi:“MI:0914”(association) | 0.350 |
| PLEKHG3 | psi-mi:“MI:0914”(association) | 0.350 | |
| RAB33A | RAB19 | psi-mi:“MI:0914”(association) | 0.350 |
| RAB19 | KRTAP10-8 | psi-mi:“MI:0915”(physical association) | 0.000 |
| RABIF | RAB19 | psi-mi:“MI:0915”(physical association) | 0.000 |
| VCAN | RAB19 | psi-mi:“MI:0915”(physical association) | 0.000 |
| LSM11 | RAB19 | psi-mi:“MI:0915”(physical association) | 0.000 |
BioGRID (11): VDAC3 (Co-fractionation), TOMM40 (Co-fractionation), VDAC1 (Co-fractionation), TOMM5 (Co-fractionation), RAB19 (Two-hybrid), LSM11 (Two-hybrid), RABIF (Two-hybrid), KRTAP10-8 (Two-hybrid), RAB19 (Proximity Label-MS), RAB19 (Affinity Capture-MS), RAB19 (Affinity Capture-MS)
ESM2 similar proteins: A4D1S5, O13876, O80501, P05714, P10948, P10949, P20337, P20338, P34213, P35289, P35293, P35294, P51152, P51159, P56371, P62823, P90726, Q05976, Q0IIG8, Q15771, Q17QB7, Q18969, Q1HE58, Q28IZ3, Q2TBH7, Q32NQ0, Q3ZC27, Q53B90, Q54E92, Q55FK2, Q5EB77, Q5KTJ7, Q5M7U5, Q5R5H5, Q63941, Q68EK7, Q6DHC1, Q6PHI9, Q8CG50, Q923S9
Diamond homologs: A4D1S5, A4FV54, F1PTE3, O04486, O24466, O76173, P01123, P10536, P11620, P16976, P17609, P20790, P20791, P22125, P22128, P28186, P28188, P31584, P33723, P34139, P34140, P35280, P35286, P35294, P36410, P36863, P40392, P51153, P51156, P53994, P55258, P59279, P61006, P61007, P61019, P61028, P61105, P62820, P62821, P62822
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
52 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 46 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
621 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 7:140411872:A:AG | acceptor_gain | 1.0000 |
| 7:140411873:G:GT | acceptor_gain | 1.0000 |
| 7:140411873:GA:G | acceptor_gain | 1.0000 |
| 7:140411873:GAT:G | acceptor_gain | 1.0000 |
| 7:140411873:GATGC:G | acceptor_gain | 1.0000 |
| 7:140412041:G:GA | donor_gain | 1.0000 |
| 7:140412053:GATTG:G | donor_gain | 1.0000 |
| 7:140412055:TTGGT:T | donor_loss | 1.0000 |
| 7:140412058:G:GG | donor_gain | 1.0000 |
| 7:140425880:A:AG | acceptor_gain | 1.0000 |
| 7:140425880:AGG:A | acceptor_loss | 1.0000 |
| 7:140425881:G:GG | acceptor_gain | 1.0000 |
| 7:140425881:GGA:G | acceptor_gain | 1.0000 |
| 7:140425881:GGAA:G | acceptor_gain | 1.0000 |
| 7:140404213:GACAG:G | donor_gain | 0.9900 |
| 7:140404219:T:G | donor_loss | 0.9900 |
| 7:140407622:A:AG | acceptor_gain | 0.9900 |
| 7:140407623:G:GG | acceptor_gain | 0.9900 |
| 7:140407797:G:GT | donor_gain | 0.9900 |
| 7:140407812:G:GG | donor_gain | 0.9900 |
| 7:140411861:T:TA | acceptor_gain | 0.9900 |
| 7:140411872:AGAT:A | acceptor_gain | 0.9900 |
| 7:140411873:GATG:G | acceptor_gain | 0.9900 |
| 7:140412058:GTAT:G | donor_loss | 0.9900 |
| 7:140412059:T:G | donor_loss | 0.9900 |
| 7:140425880:AG:A | acceptor_gain | 0.9900 |
| 7:140425881:GG:G | acceptor_gain | 0.9900 |
| 7:140425881:GGAAA:G | acceptor_gain | 0.9900 |
| 7:140407623:GTT:G | acceptor_gain | 0.9800 |
| 7:140407623:GTTCT:G | acceptor_gain | 0.9800 |
AlphaMissense
1435 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 7:140407734:A:C | K30Q | 0.999 |
| 7:140407798:G:A | G51E | 0.999 |
| 7:140411883:T:A | W71R | 0.999 |
| 7:140411883:T:C | W71R | 0.999 |
| 7:140411887:A:C | D72A | 0.999 |
| 7:140411887:A:T | D72V | 0.999 |
| 7:140411907:T:C | F79L | 0.999 |
| 7:140411909:C:A | F79L | 0.999 |
| 7:140411909:C:G | F79L | 0.999 |
| 7:140425888:A:T | K131I | 0.999 |
| 7:140407717:G:A | G24E | 0.998 |
| 7:140407717:G:T | G24V | 0.998 |
| 7:140407732:G:A | G29E | 0.998 |
| 7:140407806:T:C | F54L | 0.998 |
| 7:140407808:T:A | F54L | 0.998 |
| 7:140407808:T:G | F54L | 0.998 |
| 7:140411886:G:C | D72H | 0.998 |
| 7:140411887:A:G | D72G | 0.998 |
| 7:140411888:C:A | D72E | 0.998 |
| 7:140411888:C:G | D72E | 0.998 |
| 7:140411907:T:A | F79I | 0.998 |
| 7:140407716:G:T | G24W | 0.997 |
| 7:140407731:G:T | G29W | 0.997 |
| 7:140407732:G:T | G29V | 0.997 |
| 7:140407734:A:G | K30E | 0.997 |
| 7:140407735:A:T | K30M | 0.997 |
| 7:140407736:G:C | K30N | 0.997 |
| 7:140407736:G:T | K30N | 0.997 |
| 7:140411885:G:C | W71C | 0.997 |
| 7:140411885:G:T | W71C | 0.997 |
dbSNP variants (sampled 300 via entrez): RS1000182796 (7:140419430 C>T), RS1000263715 (7:140418737 T>G), RS1000401217 (7:140418524 C>G,T), RS1000423119 (7:140425031 A>G), RS1000612474 (7:140415105 T>C), RS1000701681 (7:140412460 A>G,T), RS1000732939 (7:140420091 G>C), RS1000892957 (7:140403872 G>A,C), RS1000899844 (7:140413888 T>C), RS1001163432 (7:140426229 C>G), RS1001222690 (7:140419883 T>C), RS1001253631 (7:140420264 T>C), RS1001411305 (7:140427016 AT>A,ATT), RS1001669964 (7:140413000 C>G), RS1001693881 (7:140425585 G>A)
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (2): non-syndromic syndactyly (MONDO:0019530), primary ovarian failure (MONDO:0005387)
Orphanet (2): Non-syndromic syndactyly (Orphanet:90025), NON RARE IN EUROPE: Primary ovarian failure (Orphanet:619)
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
1 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST009028_31 | Adverse response to drug | 3.000000e-07 |
EFO canonical traits (1, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0009658 | adverse effect |
MeSH disease descriptors (1)
| Descriptor | Name | Tree numbers |
|---|---|---|
| D016649 | Primary Ovarian Insufficiency | C12.050.351.500.056.630.750; C12.100.250.056.630.750; C19.391.630.750 |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
6 total (human), top 6 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| bisphenol A | decreases expression, increases expression, increases methylation | 3 |
| CGP 52608 | affects binding, increases reaction | 1 |
| Resveratrol | affects cotreatment, decreases expression | 1 |
| Benzo(a)pyrene | decreases methylation | 1 |
| Plant Extracts | affects cotreatment, decreases expression | 1 |
| Tobacco Smoke Pollution | affects expression | 1 |
Clinical trials (associated diseases)
79 trials via MONDO — disease-level, not drug-specific.
| Trial | Phase | Status | Title |
|---|---|---|---|
| NCT04564430 | PHASE4 | UNKNOWN | Clonidine for Tourniquet-related Pain in Children |
| NCT00417066 | PHASE4 | COMPLETED | Flexible GnRH Antagonist vs Flare up GnRH Agonist Protocol in Poor Responders |
| NCT00732693 | PHASE4 | COMPLETED | Evaluation of Physiologic and Standard Sex Steroid Replacement Regimens in Women With Premature Ovarian Failure |
| NCT00837616 | PHASE4 | COMPLETED | Estrogen Dosing in Turner Syndrome: Pharmacology and Metabolism |
| NCT01853501 | PHASE4 | UNKNOWN | Effects of ADSC Therapy in Women With POF |
| NCT02783937 | PHASE4 | COMPLETED | Filgrastim for Premature Ovarian Insufficiency |
| NCT03535480 | PHASE4 | UNKNOWN | Autologous Bone Marrow Stem Cell Ovarian Transplantation to Restore Ovarian Function in Premature Ovarian Failure |
| NCT00140998 | PHASE3 | COMPLETED | Estrogen Treatment (Oral vs. Patches) in Turner Syndrome |
| NCT00001951 | PHASE2 | COMPLETED | Hormone Replacement in Young Women With Premature Ovarian Failure |
| NCT00370019 | PHASE2 | WITHDRAWN | Effects of an Estrogen Replacement Therapy Skin Patch on Ovulation in Women With Premature Ovarian Failure |
| NCT00429494 | PHASE2 | COMPLETED | GnRH Analogue for Ovarian Function Preservation in Hematopoietic Stem Cell Transplantation Patients |
| NCT03816852 | PHASE2 | SUSPENDED | The Safety and Efficiency Study of Mesenchymal Stem Cell (19#iSCLife®-POI) in Premature Ovarian Insufficiency |
| NCT04536467 | PHASE2 | UNKNOWN | Prevention of Chemotherapy-Induced Ovarian Failure With Goserelin in Premenopausal Lymphoma Patients |
| NCT06117982 | PHASE2 | COMPLETED | The Impact of Granulocyte Colony Stimulating Factor on Premature Ovarian Insufficiency |
| NCT02912104 | PHASE1 | COMPLETED | A Therapeutic Trial of Human Amniotic Epithelial Cells Transplantation for Primary Ovarian Failure |
| NCT03178695 | PHASE1 | COMPLETED | Inovium Ovarian Rejuvenation Trials |
| NCT04815213 | PHASE1 | ACTIVE_NOT_RECRUITING | The Use of Expandeded Mesenchymal Stromal Cells (MSC) in Premature Ovarian Failure (POF) in Adult Humans |
| NCT05138367 | PHASE1 | COMPLETED | Effects of UCA-PSCs in Women With POF |
| NCT06132542 | PHASE1 | UNKNOWN | Autologous ADMSC Transplantation in Patients With POI |
| NCT03107546 | Not specified | COMPLETED | Comparison of Scar Formation in Syndactyly Release Surgery With Full Thickness Skin Graft Versus Skin Graft Substitute |
| NCT06239064 | Not specified | ACTIVE_NOT_RECRUITING | Early Genetic Identification of Obesity |
| NCT07596862 | Not specified | COMPLETED | Remote Assesment of Functional Sequelae in Patients Operated for Congenital Syndactyly |
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| NCT02644447 | PHASE1/PHASE2 | COMPLETED | Transplantation of HUC-MSCs With Injectable Collagen Scaffold for POF |
| NCT03069209 | PHASE1/PHASE2 | UNKNOWN | Autologous Bone Marrow-Derived Stem Cell Transplantation in Patients With Premature Ovarian Failure (POF) |
| NCT03985462 | PHASE1/PHASE2 | WITHDRAWN | Very Small Embryonic-like Stem Cells for Ovary |
| NCT04009473 | PHASE1/PHASE2 | UNKNOWN | Stem Cell Therapy and Growth Factor Ovarian in Vitro Activation |
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| NCT05462379 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | Autologous Heterotopic Fresh Ovarian Graft in Woman With LACC Eligible for Pelvic Radiotherapy Treatment. |
| NCT06202547 | PHASE1/PHASE2 | UNKNOWN | Intra-ovarian Injection of MSC-EVs in Idiopathic Premature Ovarian Failure |
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Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): non-syndromic syndactyly