DNAJC22

gene
On this page

Also known as wusFLJ13236

Summary

DNAJC22 (DnaJ heat shock protein family (Hsp40) member C22, HGNC:25802) is a protein-coding gene on chromosome 12q13.12, encoding DnaJ homolog subfamily C member 22 (Q8N4W6). May function as a co-chaperone.

Predicted to be active in membrane.

Source: NCBI Gene 79962 — RefSeq curated summary.

At a glance

  • GWAS associations: 6
  • Clinical variants (ClinVar): 66 total
  • MANE Select transcript: NM_001304944

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25802
Approved symbolDNAJC22
NameDnaJ heat shock protein family (Hsp40) member C22
Location12q13.12
Locus typegene with protein product
StatusApproved
Aliaseswus, FLJ13236
Ensembl geneENSG00000178401
Ensembl biotypeprotein_coding
Entrez79962

Gene structure

Transcript identifiers

Ensembl transcripts: 8 — 5 protein_coding, 1 retained_intron, 1 protein_coding_CDS_not_defined, 1 nonsense_mediated_decay

ENST00000395069, ENST00000549441, ENST00000551153, ENST00000552651, ENST00000647553, ENST00000851339, ENST00000851340, ENST00000851341

RefSeq mRNA: 2 — MANE Select: NM_001304944 NM_001304944, NM_024902

CCDS: CCDS8785

Canonical transcript exons

ENST00000549441 — 4 exons

ExonStartEnd
ENSE000012645644934876649349712
ENSE000015204844935131749353690
ENSE000023306424934764449348105
ENSE000023670864934688849347551

Expression profiles

Bgee: expression breadth ubiquitous, 238 present calls, max score 94.90.

FANTOM5 (CAGE): breadth broad, TPM avg 1.9728 / max 39.2197, expressed in 673 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
1253291.5095605
1253280.1999121
1253270.1965113
1253300.066927

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right lobe of liverUBERON:000111494.90gold quality
liverUBERON:000210791.00gold quality
heart right ventricleUBERON:000208090.69silver quality
jejunal mucosaUBERON:000039989.82gold quality
body of tongueUBERON:001187689.72silver quality
lateral nuclear group of thalamusUBERON:000273689.56silver quality
skeletal muscle tissue of rectus abdominisUBERON:000451189.40silver quality
vena cavaUBERON:000408789.28silver quality
ponsUBERON:000098888.95gold quality
subthalamic nucleusUBERON:000190688.69gold quality
cardia of stomachUBERON:000116288.66silver quality
duodenumUBERON:000211488.61gold quality
pylorusUBERON:000116688.14gold quality
inferior vagus X ganglionUBERON:000536388.00silver quality
jejunumUBERON:000211587.97gold quality
ventral tegmental areaUBERON:000269187.74silver quality
lateral globus pallidusUBERON:000247687.33gold quality
pharyngeal mucosaUBERON:000035587.20silver quality
pancreatic ductal cellCL:000207986.98silver quality
mucosa of transverse colonUBERON:000499186.95gold quality
tongueUBERON:000172386.74silver quality
pericardiumUBERON:000240786.60silver quality
superior vestibular nucleusUBERON:000722786.49silver quality
substantia nigra pars reticulataUBERON:000196686.41gold quality
superior surface of tongueUBERON:000737186.41silver quality
endometrium epitheliumUBERON:000481186.20gold quality
substantia nigra pars compactaUBERON:000196586.19silver quality
gall bladderUBERON:000211085.86gold quality
renal medullaUBERON:000036285.77gold quality
saphenous veinUBERON:000731885.18silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.50

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

83 targeting DNAJC22, 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-4425100.0067.591049
HSA-MIR-3163100.0077.238605
HSA-MIR-5011-5P100.0083.465820
HSA-MIR-6798-5P100.0065.77699
HSA-MIR-5692B100.0071.322622
HSA-MIR-5692C100.0071.322622
HSA-MIR-150-5P99.9966.691976
HSA-MIR-453199.9969.703181
HSA-MIR-477599.9875.006394
HSA-MIR-302C-5P99.9772.563642
HSA-MIR-365899.9673.874379
HSA-MIR-302E99.9670.742669
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-3912-5P99.9566.11925
HSA-MIR-374A-5P99.9071.342923
HSA-MIR-374B-5P99.9069.982734
HSA-MIR-124-3P99.8973.743043
HSA-MIR-506-3P99.8973.553057
HSA-MIR-990299.8969.152250
HSA-MIR-7845-5P99.8864.88771
HSA-MIR-576-5P99.8470.462582
HSA-MIR-6756-5P99.8267.972466
HSA-MIR-4694-3P99.7969.532640
HSA-MIR-4713-5P99.7867.801794
HSA-MIR-3913-5P99.7867.26968
HSA-MIR-2116-3P99.7464.32889
HSA-MIR-674599.7465.331321
HSA-MIR-4524A-3P99.7266.852406
HSA-MIR-6766-5P99.6867.702325
HSA-MIR-46699.6770.852863

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriodnajc22ENSDARG00000037067
mus_musculusDnajc22ENSMUSG00000038009
rattus_norvegicusDnajc22ENSRNOG00000053498
drosophila_melanogasterwusFBGN0030805

Protein

Protein identifiers

DnaJ homolog subfamily C member 22Q8N4W6 (reviewed: Q8N4W6)

All UniProt accessions (1): Q8N4W6

UniProt curated annotations — full annotation on UniProt →

Function. May function as a co-chaperone.

Subcellular location. Membrane.

RefSeq proteins (2): NP_001291873, NP_079178 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001623DnaJ_domainDomain
IPR007829TM2Domain
IPR036869J_dom_sfHomologous_superfamily

Pfam: PF00226, PF05154

UniProt features (10 total): transmembrane region 7, domain 2, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8N4W6-F181.460.39

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 122 (showing top): MORF_ITGA2, WANG_CLIM2_TARGETS_UP, BENPORATH_ES_WITH_H3K27ME3, NKX25_02, LUCAS_HNF4A_TARGETS_UP, MORF_RAD51L3, MODULE_205, MORF_CTSB, YY1_02, ROZANOV_MMP14_TARGETS_UP, MORF_IL4, MORF_PRKCA, HNF4_DR1_Q3, MORF_THPO, MORF_ATF2

GO Biological Process (0):

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (1): membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding1
cellular anatomical structure1

Protein interactions and networks

STRING

1671 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
DNAJC22DNAJC18Q9H819559
DNAJC22DNAJC28Q9NX36558
DNAJC22DNAJC9Q8WXX5552
DNAJC22DNAJC27Q9NZQ0545
DNAJC22DNAJC24Q6P3W2540
DNAJC22DNAJC25Q9H1X3511
DNAJC22LBX1P52954510
DNAJC22DNAJC8O75937495
DNAJC22LMBR1LQ6UX01490
DNAJC22DNAJB13P59910472
DNAJC22DNAJC4Q9NNZ3463
DNAJC22DNAJC13O75165448
DNAJC22DNAJC1Q96KC8448
DNAJC22DNAJC2Q99543446
DNAJC22SEPTIN3Q9UH03445

IntAct

6 interactions, top by confidence:

ABTypeScore
MEOX2DNAJC22psi-mi:“MI:0915”(physical association)0.560
DNAJC22UNC13Bpsi-mi:“MI:0914”(association)0.350
LYPD3NEMP1psi-mi:“MI:0914”(association)0.350
DNAJC22MEOX2psi-mi:“MI:0915”(physical association)0.000

BioGRID (39): DNAJC22 (Two-hybrid), ENSA (Affinity Capture-MS), RPN1 (Affinity Capture-MS), SDHA (Affinity Capture-MS), RANBP3 (Affinity Capture-MS), CMAS (Affinity Capture-MS), LARP7 (Affinity Capture-MS), TRIM13 (Proximity Label-MS), CKAP4 (Proximity Label-MS), ADCY9 (Proximity Label-MS), TMEM199 (Proximity Label-MS), ECH1 (Proximity Label-MS), EMD (Proximity Label-MS), STT3B (Proximity Label-MS), EMC1 (Proximity Label-MS)

ESM2 similar proteins: A9ULE9, B0K025, B1X3F0, E2RKN8, F1LXS7, O06752, O24301, O28116, O29246, O30092, P18033, P27709, P29574, P31924, P49036, P55522, P61165, P61166, P64445, P64446, P64447, P86218, Q01390, Q17QW0, Q28IL7, Q2HJ69, Q2KID7, Q32P84, Q3AKY6, Q3AYG7, Q43009, Q57938, Q5M9B7, Q5PR00, Q5RBD7, Q5ZJR3, Q5ZLR7, Q6GLZ9, Q6GNY6, Q6PBS6

Diamond homologs: A0A0P0VG31, A5IIT4, A9ULE9, B1LCI2, B7IFE0, B9KAB9, Q17QW0, Q54YM7, Q5PR00, Q5RBD7, Q8CHS2, Q8N4W6, Q97BG9, Q9GPR3, Q9HJ83, Q9WZV3, A0Q1R3, A4XKA5, A5EYE5, A6LJ63, A9VHU0, B0SHT0, B0SRF0, B2TLZ8, B2V2I6, B7HCT9, B7HPL2, B7IYG6, B7JN38, B9E6X0, B9IY80, B9MJZ0, C1ESK7, C3L5R6, C3P8L9, O35723, O54946, O75190, O94625, P30725

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance56
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

749 predictions. Top by Δscore:

VariantEffectΔscore
12:49347198:G:GTdonor_gain1.0000
12:49347199:A:Tdonor_gain1.0000
12:49349713:GTAA:Gdonor_loss1.0000
12:49351312:A:AGacceptor_gain1.0000
12:49351312:ATAAG:Aacceptor_gain1.0000
12:49351313:T:Gacceptor_gain1.0000
12:49351314:A:AGacceptor_gain1.0000
12:49351314:AAG:Aacceptor_gain1.0000
12:49351315:A:Gacceptor_gain1.0000
12:49347549:GAGG:Gdonor_loss0.9900
12:49347550:AGGT:Adonor_loss0.9900
12:49347552:GTGAG:Gdonor_loss0.9900
12:49347553:T:Adonor_loss0.9900
12:49348872:G:GTdonor_gain0.9900
12:49349593:C:Aacceptor_gain0.9900
12:49349714:T:Gdonor_loss0.9900
12:49351313:TAA:Tacceptor_loss0.9900
12:49351315:A:ACacceptor_loss0.9900
12:49351316:G:Aacceptor_gain0.9900
12:49351316:G:GGacceptor_gain0.9900
12:49351316:GG:Gacceptor_loss0.9900
12:49347116:G:GTdonor_gain0.9800
12:49347552:G:GGdonor_gain0.9800
12:49347557:G:GTdonor_gain0.9800
12:49347558:G:Tdonor_gain0.9800
12:49348764:AG:Aacceptor_gain0.9800
12:49348765:GG:Gacceptor_gain0.9800
12:49348834:C:Tdonor_gain0.9800
12:49348837:G:GGdonor_gain0.9800
12:49349713:G:GGdonor_gain0.9800

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000174322 (12:49346525 C>G), RS1000204610 (12:49347873 A>C), RS1000278259 (12:49348186 C>A,T), RS1000796956 (12:49351339 C>A,T), RS1001275416 (12:49347298 C>G), RS1001569756 (12:49353823 C>T), RS1001580795 (12:49347560 G>A), RS1001793811 (12:49352762 A>G), RS1001857595 (12:49347837 C>T), RS1002305202 (12:49348666 A>T), RS1002336416 (12:49348999 C>A,G,T), RS1003117365 (12:49346723 T>C), RS1003282586 (12:49349858 G>C), RS1003598785 (12:49350165 C>T), RS1004148071 (12:49348115 C>T)

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

6 associations (top):

StudyTraitp-value
GCST008075_191HDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df)3.000000e-08
GCST008075_73HDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df)1.000000e-08
GCST008084_175HDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df)2.000000e-07
GCST008084_97HDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df)3.000000e-08
GCST008085_171HDL cholesterol levels in current drinkers4.000000e-08
GCST008085_93HDL cholesterol levels in current drinkers2.000000e-08

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0004612high density lipoprotein cholesterol measurement
EFO:0004329alcohol drinking

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

26 total (human), top 26 by PubMed support.

ChemicalActions (top 5)PubMed papers
Tetrachlorodibenzodioxinaffects expression, increases expression3
sodium arseniteincreases expression, increases abundance2
Cyclosporinedecreases expression2
pirinixic acidaffects binding, decreases expression, increases activity1
2-methyl-4-isothiazolin-3-oneincreases expression1
manganese chlorideincreases abundance, increases expression1
abrinedecreases expression1
(+)-JQ1 compounddecreases expression1
Vorinostatdecreases expression1
Acetaminophendecreases expression1
Arsenicincreases abundance, increases expression1
Benzo(a)pyreneaffects methylation, decreases methylation1
Estradioldecreases expression1
Formaldehydeincreases expression1
Hydrogen Peroxideaffects expression1
Manganeseincreases abundance, increases expression1
Niclosamideincreases expression1
Rotenonedecreases expression1
Silicon Dioxidedecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Triclosanincreases expression1
Valproic Aciddecreases expression1
1-Methyl-4-phenylpyridiniumdecreases expression1
Cadmium Chloridedecreases expression1
Copper Sulfatedecreases expression1
Particulate Matterincreases expression1

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.