DNAJC25

gene
On this page

Also known as bA16L21.2.1

Summary

DNAJC25 (DnaJ heat shock protein family (Hsp40) member C25, HGNC:34187) is a protein-coding gene on chromosome 9q31.3, encoding DnaJ homolog subfamily C member 25 (Q9H1X3).

Predicted to be involved in protein folding. Predicted to be located in membrane. Predicted to be active in endoplasmic reticulum membrane.

Source: NCBI Gene 548645 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 16 total
  • MANE Select transcript: NM_001015882

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:34187
Approved symbolDNAJC25
NameDnaJ heat shock protein family (Hsp40) member C25
Location9q31.3
Locus typegene with protein product
StatusApproved
AliasesbA16L21.2.1
Ensembl geneENSG00000059769
Ensembl biotypeprotein_coding
Entrez548645

Gene structure

Transcript identifiers

Ensembl transcripts: 6 — 4 protein_coding, 2 nonsense_mediated_decay

ENST00000313525, ENST00000447096, ENST00000463589, ENST00000905074, ENST00000905075, ENST00000905076

RefSeq mRNA: 1 — MANE Select: NM_001015882 NM_001015882

CCDS: CCDS43862

Canonical transcript exons

ENST00000313525 — 4 exons

ExonStartEnd
ENSE00001519553111631334111631743
ENSE00003543457111653100111654345
ENSE00003636179111647107111647259
ENSE00003670574111649453111649923

Expression profiles

Bgee: expression breadth ubiquitous, 256 present calls, max score 96.32.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 7.0045 / max 348.3202, expressed in 1707 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
980168.35491797
980177.00451707

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
epithelial cell of pancreasCL:000008396.32gold quality
pancreatic ductal cellCL:000207992.42gold quality
right lobe of liverUBERON:000111490.78gold quality
liverUBERON:000210789.81gold quality
cartilage tissueUBERON:000241887.36gold quality
germinal epithelium of ovaryUBERON:000130486.33gold quality
left adrenal glandUBERON:000123484.78gold quality
left ventricle myocardiumUBERON:000656684.41silver quality
left adrenal gland cortexUBERON:003582584.35gold quality
right adrenal gland cortexUBERON:003582784.08gold quality
kidney epitheliumUBERON:000481984.02silver quality
calcaneal tendonUBERON:000370184.00gold quality
right adrenal glandUBERON:000123383.83gold quality
adrenal cortexUBERON:000123583.76gold quality
adrenal glandUBERON:000236983.50gold quality
islet of LangerhansUBERON:000000682.10gold quality
tibiaUBERON:000097981.32gold quality
stromal cell of endometriumCL:000225580.99gold quality
parietal pleuraUBERON:000240080.97gold quality
pigmented layer of retinaUBERON:000178280.79gold quality
ileal mucosaUBERON:000033180.62gold quality
omental fat padUBERON:001041480.46gold quality
peritoneumUBERON:000235880.43gold quality
adrenal tissueUBERON:001830380.34gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099180.05gold quality
adipose tissue of abdominal regionUBERON:000780880.02gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047380.00gold quality
pancreasUBERON:000126479.74gold quality
lower esophagus mucosaUBERON:003583479.41gold quality
adult mammalian kidneyUBERON:000008279.08gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.39

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

91 targeting DNAJC25, 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-340-5P100.0072.504437
HSA-MIR-3163100.0077.238605
HSA-MIR-3924100.0072.092394
HSA-MIR-656-3P100.0072.152788
HSA-MIR-6758-5P100.0066.211470
HSA-MIR-5692B100.0071.322622
HSA-MIR-5692C100.0071.322622
HSA-MIR-6856-5P100.0065.471298
HSA-MIR-5692A100.0074.406850
HSA-MIR-4789-3P99.9970.752484
HSA-MIR-428299.9975.366408
HSA-MIR-453199.9969.703181
HSA-MIR-499A-5P99.9870.791323
HSA-MIR-56899.9869.862084
HSA-MIR-548AT-5P99.9670.832666
HSA-MIR-570-3P99.9672.414910
HSA-MIR-568099.9169.833421
HSA-MIR-367199.9073.043897
HSA-MIR-374A-5P99.9071.342923
HSA-MIR-374B-5P99.9069.982734
HSA-MIR-808799.9069.551351
HSA-MIR-576-5P99.8470.462582
HSA-MIR-4799-5P99.8270.602663
HSA-MIR-129999.7771.242389
HSA-MIR-451799.7669.191867
HSA-MIR-7856-5P99.7569.992901
HSA-MIR-197699.7465.481127
HSA-MIR-430699.7270.503630
HSA-MIR-4699-3P99.7170.153142
HSA-MIR-580-3P99.6769.231841

Cross-species orthologs

8 orthologs

OrganismSymbolGene ID
danio_reriodnajc25ENSDARG00000067613
mus_musculusDnajc25ENSMUSG00000070972
rattus_norvegicusDnajc25ENSRNOG00000015340
drosophila_melanogasterCG7872FBGN0030658
caenorhabditis_elegansWBGENE00001020
caenorhabditis_elegansWBGENE00001025
caenorhabditis_elegansdnj-28WBGENE00001046
caenorhabditis_elegansWBGENE00008122

Paralogs (20): DNAJC11 (ENSG00000007923), DNAJC10 (ENSG00000077232), DNAJC5 (ENSG00000101152), DNAJC3 (ENSG00000102580), DNAJC17 (ENSG00000104129), DNAJC2 (ENSG00000105821), DNAJC12 (ENSG00000108176), DNAJC4 (ENSG00000110011), DNAJC16 (ENSG00000116138), DNAJC14 (ENSG00000135392), DNAJC1 (ENSG00000136770), DNAJC13 (ENSG00000138246), DNAJC5B (ENSG00000147570), DNAJC5G (ENSG00000163793), DNAJC7 (ENSG00000168259), DNAJC21 (ENSG00000168724), DNAJC18 (ENSG00000170464), DNAJC24 (ENSG00000170946), DNAJC30 (ENSG00000176410), DNAJC9 (ENSG00000213551)

Protein

Protein identifiers

DnaJ homolog subfamily C member 25Q9H1X3 (reviewed: Q9H1X3)

All UniProt accessions (3): Q9H1X3, F2Z3D1, J3QR79

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the DNAJC25 family.

Isoforms (3)

UniProt IDNamesCanonical?
Q9H1X3-11yes
Q9H1X3-22
Q9H1X3-33

RefSeq proteins (1): NP_001015882* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001623DnaJ_domainDomain
IPR036869J_dom_sfHomologous_superfamily
IPR044632DNAJC25-likeFamily

Pfam: PF00226

UniProt features (8 total): transmembrane region 3, splice variant 3, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9H1X3-F183.630.54

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 90 (showing top): GOBP_PROTEIN_MATURATION, GOBP_PROTEIN_FOLDING, ACTTTAT_MIR1425P, GOCC_NUCLEAR_OUTER_MEMBRANE_ENDOPLASMIC_RETICULUM_MEMBRANE_NETWORK, GOCC_ORGANELLE_SUBCOMPARTMENT, KOINUMA_TARGETS_OF_SMAD2_OR_SMAD3, ALKBH3_TARGET_GENES, DACH1_TARGET_GENES, DIDO1_TARGET_GENES, DROSHA_TARGET_GENES, E2F2_TARGET_GENES, FOXN3_TARGET_GENES, GLI4_TARGET_GENES, KLF7_TARGET_GENES, NKX2_3_TARGET_GENES

GO Biological Process (1): protein folding (GO:0006457)

GO Molecular Function (0):

GO Cellular Component (2): endoplasmic reticulum membrane (GO:0005789), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular process1
protein maturation1
organelle membrane1
nuclear outer membrane-endoplasmic reticulum membrane network1
endoplasmic reticulum subcompartment1
cellular anatomical structure1

Protein interactions and networks

STRING

2001 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
DNAJC25DNAJC9Q8WXX5639
DNAJC25DNAJC8O75937585
DNAJC25DNAJC27Q9NZQ0550
DNAJC25DNAJC12Q9UKB3541
DNAJC25HSPA4P34932535
DNAJC25DNAJC28Q9NX36524
DNAJC25DNAJC22Q8N4W6511
DNAJC25DNAJC15Q9Y5T4497
DNAJC25DNAJC2Q99543449
DNAJC25FBXO36Q8NEA4428
DNAJC25CTXN1P60606420
DNAJC25DNAJC7Q99615415
DNAJC25DNAJC13O75165402
DNAJC25SPATS1Q496A3400
DNAJC25PIH1D2Q8WWB5398

IntAct

11 interactions, top by confidence:

ABTypeScore
CXCR4TMEM120Bpsi-mi:“MI:0914”(association)0.530
Sesn2CASTOR2psi-mi:“MI:0914”(association)0.350
Mpsi-mi:“MI:0914”(association)0.350
RAMP2GXYLT2psi-mi:“MI:0914”(association)0.350
CMTM5TMEM120Bpsi-mi:“MI:0914”(association)0.350
DNAJC25BRCC3psi-mi:“MI:0914”(association)0.350
DNAJC25TUBAL3psi-mi:“MI:0914”(association)0.350
TMEM169PTGES3L-AARSD1psi-mi:“MI:0914”(association)0.350
SLC15A3GXYLT2psi-mi:“MI:0914”(association)0.350
SLC39A14ESYT2psi-mi:“MI:0914”(association)0.350

BioGRID (314): DNAJC25 (Affinity Capture-MS), DNAJC25 (Proximity Label-MS), DNAJC25 (Proximity Label-MS), HAX1 (Affinity Capture-MS), NOP56 (Affinity Capture-MS), YME1L1 (Affinity Capture-MS), PGRMC1 (Affinity Capture-MS), SEC61B (Affinity Capture-MS), DNMT1 (Affinity Capture-MS), EMD (Affinity Capture-MS), PPP6R1 (Affinity Capture-MS), SPG20 (Affinity Capture-MS), SIRT1 (Affinity Capture-MS), RPL13A (Affinity Capture-MS), SRRM2 (Affinity Capture-MS)

ESM2 similar proteins: A1A4P4, A1CH36, A2ALW5, A5AAL8, B0BN56, O42911, O70279, P0C2B7, P58468, P83565, Q0CLE8, Q1ECT8, Q290P4, Q2GVC2, Q3SZ86, Q4G0I0, Q4V7Q1, Q5B4U6, Q5BJW9, Q5RFR4, Q5XJW2, Q61733, Q6RUT7, Q753F1, Q7SDU5, Q7SHR9, Q80ZS3, Q86TS9, Q8BGX2, Q8BK72, Q8CHP5, Q8SPE7, Q8TAE8, Q8VD26, Q8WUQ7, Q96AN5, Q96DF8, Q9BRP8, Q9BSF4, Q9BYN8

Diamond homologs: A0LJ41, A1V9Q3, A1WAR7, A1WX30, A2ALW5, A3DF24, A4IR30, A5ITA7, A5WBF8, A6QHC2, A6U251, A7GT07, A7X2Y0, A7Z6W0, A8FFD1, A8Z4B8, A9KE65, A9NDK6, A9VHU0, B0JW23, B0VQ00, B1HUD0, B1WVR2, B1Y787, B1YKT0, B2GBQ6, B2I2G6, B2J3J3, B3EE31, B7GV08, B7HPL2, B7I2B2, B7JN38, B8CXL0, B8FUN3, B9DNJ9, B9IY80, C1ESK7, C3L5R6, C3P8L9

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance16
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1015 predictions. Top by Δscore:

VariantEffectΔscore
9:111631740:CAAGG:Cdonor_loss1.0000
9:111631741:AAGGT:Adonor_loss1.0000
9:111631742:AGG:Adonor_loss1.0000
9:111631743:GGT:Gdonor_loss1.0000
9:111631744:G:GAdonor_loss1.0000
9:111631745:T:Adonor_loss1.0000
9:111631745:T:Gdonor_loss1.0000
9:111632592:G:GTdonor_gain1.0000
9:111647101:TTACA:Tacceptor_loss1.0000
9:111647102:TACA:Tacceptor_loss1.0000
9:111647103:A:AGacceptor_gain1.0000
9:111647104:CA:Cacceptor_loss1.0000
9:111647104:CAGGA:Cacceptor_loss1.0000
9:111647105:A:AGacceptor_gain1.0000
9:111647105:AG:Aacceptor_gain1.0000
9:111647105:AGG:Aacceptor_loss1.0000
9:111647106:G:GAacceptor_gain1.0000
9:111647106:G:GGacceptor_gain1.0000
9:111647106:GG:Gacceptor_gain1.0000
9:111647106:GGAT:Gacceptor_gain1.0000
9:111647258:AGG:Adonor_loss1.0000
9:111647259:GGT:Gdonor_loss1.0000
9:111647260:G:GAdonor_loss1.0000
9:111647260:G:GGdonor_gain1.0000
9:111647261:T:Gdonor_loss1.0000
9:111649451:A:AGacceptor_gain1.0000
9:111649452:G:GTacceptor_gain1.0000
9:111649452:GT:Gacceptor_gain1.0000
9:111649452:GTT:Gacceptor_gain1.0000
9:111649615:G:GTdonor_gain1.0000

AlphaMissense

2347 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
9:111631739:T:AL111H0.999
9:111631708:T:CF101L0.998
9:111631710:C:AF101L0.998
9:111631710:C:GF101L0.998
9:111647120:G:CR117P0.998
9:111647233:A:CS155R0.998
9:111647235:C:AS155R0.998
9:111647235:C:GS155R0.998
9:111649517:G:CR185P0.998
9:111631636:C:GH77D0.997
9:111631727:C:AA107D0.997
9:111631739:T:CL111P0.997
9:111649525:G:CA188P0.997
9:111653174:A:CR345S0.997
9:111653174:A:TR345S0.997
9:111631612:T:GY69D0.996
9:111631625:C:AA73D0.996
9:111649538:C:AA192D0.996
9:111649903:T:AW314R0.996
9:111649903:T:CW314R0.996
9:111653173:G:CR345T0.996
9:111631555:T:CC50R0.995
9:111631557:C:GC50W0.995
9:111631638:C:AH77Q0.995
9:111631638:C:GH77Q0.995
9:111631709:T:GF101C0.995
9:111631720:G:CA105P0.995
9:111649526:C:AA188D0.995
9:111653171:G:CR344S0.995
9:111653171:G:TR344S0.995

dbSNP variants (sampled 300 via entrez): RS1000459009 (9:111634178 G>A), RS1000810321 (9:111634482 G>A,C), RS1000841848 (9:111654599 G>A,T), RS1000843696 (9:111653449 T>G), RS1000915842 (9:111647010 T>C), RS1001120179 (9:111647534 C>T), RS1001205123 (9:111637945 T>C), RS1001210309 (9:111646770 C>T), RS1001346544 (9:111643433 C>A,T), RS1001357782 (9:111646006 G>T), RS1001397442 (9:111643134 C>T), RS1001429589 (9:111646423 T>C), RS1001981861 (9:111634892 A>G), RS1002172500 (9:111648375 C>T), RS1002300412 (9:111642436 A>C)

Disease associations

OMIM: gene `` | 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

21 total (human), top 21 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arseniteincreases abundance, increases expression2
Cyclosporineincreases expression2
GSK-J4increases expression1
triphenyl phosphateaffects expression1
glycidyl methacrylatedecreases expression1
zinc chromateincreases abundance, increases expression1
chromium hexavalent ionincreases abundance, increases expression1
2-palmitoylglycerolincreases expression1
K 7174increases expression1
abrineincreases expression1
PCI 5002affects cotreatment, increases expression1
Air Pollutantsdecreases expression, increases abundance1
Arsenicincreases abundance, increases expression1
Benzo(a)pyrenedecreases expression1
Thiramincreases expression1
Tobacco Smoke Pollutionincreases expression1
Tunicamycinincreases expression1
Valproic Acidincreases expression1
Zincaffects cotreatment, increases expression1
Aflatoxin B1decreases expression, decreases methylation1
Particulate Matterdecreases expression, increases abundance1

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.