DRC11
gene geneOn this page
Also known as FLJ22527
Summary
DRC11 (dynein regulatory complex subunit 11, HGNC:26195) is a protein-coding gene on chromosome 2q37.2-q37.3, encoding Dynein regulatory complex subunit 11 (Q86XH1). Component of the nexin-dynein regulatory complex (N-DRC), a key regulator of ciliary/flagellar motility which maintains the alignment and integrity of the distal axoneme and regulates microtubule sliding in motile axonemes.
The protein encoded by this gene is a member of the ATPases Associated with diverse cellular Activities (AAA) superfamily. Members of this superfamily, found in all organisms, participate in a large number of cellular processes and contain the ATPase module consisting of an alpha-beta-alpha core domain and the Walker A and B motifs of the P-loop NTPases. Alternative splicing results in multiple transcript variants that encode different protein isoforms.
Source: NCBI Gene 79781 — RefSeq curated summary.
At a glance
- GWAS associations: 1
- Clinical variants (ClinVar): 89 total
- MANE Select transcript:
NM_024726
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:26195 |
| Approved symbol | DRC11 |
| Name | dynein regulatory complex subunit 11 |
| Location | 2q37.2-q37.3 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | FLJ22527 |
| Ensembl gene | ENSG00000132321 |
| Ensembl biotype | protein_coding |
| Entrez | 79781 |
Gene structure
Transcript identifiers
Ensembl transcripts: 13 — 7 protein_coding, 3 protein_coding_CDS_not_defined, 2 retained_intron, 1 nonsense_mediated_decay
ENST00000254653, ENST00000309507, ENST00000409100, ENST00000409907, ENST00000418802, ENST00000431676, ENST00000465621, ENST00000467572, ENST00000479471, ENST00000479783, ENST00000857593, ENST00000857594, ENST00000919534
RefSeq mRNA: 3 — MANE Select: NM_024726
NM_001270584, NM_001270585, NM_024726
CCDS: CCDS46549, CCDS59441, CCDS74677
Canonical transcript exons
ENST00000409907 — 19 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001036378 | 236377103 | 236377185 |
| ENSE00001036384 | 236368194 | 236368301 |
| ENSE00001036387 | 236363780 | 236363979 |
| ENSE00001073615 | 236488000 | 236488191 |
| ENSE00001073625 | 236465505 | 236465710 |
| ENSE00001270370 | 236486829 | 236486900 |
| ENSE00001270387 | 236493768 | 236493887 |
| ENSE00001584437 | 236380569 | 236380633 |
| ENSE00001905180 | 236507257 | 236507476 |
| ENSE00003470651 | 236338205 | 236338382 |
| ENSE00003516048 | 236399413 | 236399488 |
| ENSE00003554235 | 236331359 | 236331597 |
| ENSE00003560106 | 236419149 | 236419271 |
| ENSE00003621529 | 236344557 | 236344643 |
| ENSE00003630372 | 236391976 | 236392071 |
| ENSE00003637010 | 236392244 | 236392350 |
| ENSE00003675637 | 236441040 | 236441124 |
| ENSE00003681200 | 236324151 | 236324783 |
| ENSE00003727278 | 236497163 | 236497487 |
Expression profiles
Bgee: expression breadth ubiquitous, 218 present calls, max score 98.77.
FANTOM5 (CAGE): breadth broad, TPM avg 3.3670 / max 162.0869, expressed in 568 samples.
FANTOM5 promoters (4 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 34661 | 2.6449 | 546 |
| 34663 | 0.4746 | 169 |
| 34662 | 0.1276 | 75 |
| 34660 | 0.1199 | 52 |
Top tissues by expression
286 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sperm | CL:0000019 | 98.77 | gold quality |
| male germ cell | CL:0000015 | 95.93 | gold quality |
| bronchial epithelial cell | CL:0002328 | 94.67 | gold quality |
| oocyte | CL:0000023 | 93.62 | gold quality |
| secondary oocyte | CL:0000655 | 92.94 | gold quality |
| epithelium of bronchus | UBERON:0002031 | 91.57 | gold quality |
| right uterine tube | UBERON:0001302 | 91.45 | gold quality |
| caudate nucleus | UBERON:0001873 | 90.85 | gold quality |
| bronchus | UBERON:0002185 | 90.67 | gold quality |
| medial globus pallidus | UBERON:0002477 | 90.62 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 90.58 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 90.39 | gold quality |
| thyroid gland | UBERON:0002046 | 90.20 | gold quality |
| mucosa of paranasal sinus | UBERON:0005030 | 90.05 | gold quality |
| Brodmann (1909) area 23 | UBERON:0013554 | 89.63 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 89.44 | gold quality |
| putamen | UBERON:0001874 | 89.04 | gold quality |
| globus pallidus | UBERON:0001875 | 88.79 | gold quality |
| germinal epithelium of ovary | UBERON:0001304 | 88.71 | gold quality |
| nucleus accumbens | UBERON:0001882 | 88.50 | gold quality |
| lateral globus pallidus | UBERON:0002476 | 86.60 | gold quality |
| amygdala | UBERON:0001876 | 86.10 | gold quality |
| middle temporal gyrus | UBERON:0002771 | 85.97 | gold quality |
| primary visual cortex | UBERON:0002436 | 85.53 | gold quality |
| pituitary gland | UBERON:0000007 | 85.40 | gold quality |
| adenohypophysis | UBERON:0002196 | 85.08 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 83.87 | gold quality |
| cingulate cortex | UBERON:0003027 | 83.80 | gold quality |
| hypothalamus | UBERON:0001898 | 83.57 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 83.49 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 8.10 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
17 targeting DRC11, 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-3163 | 100.00 | 77.23 | 8605 |
| HSA-MIR-9-3P | 99.96 | 70.88 | 2068 |
| HSA-MIR-9983-3P | 99.94 | 71.48 | 3631 |
| HSA-MIR-627-3P | 99.90 | 71.42 | 3316 |
| HSA-MIR-4802-3P | 99.72 | 70.13 | 1273 |
| HSA-MIR-549A-3P | 99.54 | 68.17 | 825 |
| HSA-MIR-4318 | 99.38 | 66.94 | 1505 |
| HSA-MIR-3978 | 99.24 | 68.39 | 2201 |
| HSA-MIR-4528 | 99.18 | 69.77 | 1936 |
| HSA-MIR-661 | 99.09 | 65.94 | 2062 |
| HSA-MIR-4477A | 98.83 | 69.75 | 2952 |
| HSA-MIR-7114-5P | 98.51 | 67.87 | 1349 |
| HSA-MIR-6773-3P | 98.17 | 65.51 | 1213 |
| HSA-MIR-1278 | 97.75 | 67.55 | 628 |
| HSA-MIR-708-3P | 97.50 | 68.67 | 1082 |
| HSA-MIR-890 | 97.47 | 68.67 | 982 |
| HSA-MIR-490-5P | 96.75 | 65.81 | 661 |
Cross-species orthologs
5 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | iqca1 | ENSDARG00000057276 |
| mus_musculus | Iqca1 | ENSMUSG00000026301 |
| rattus_norvegicus | Iqca1 | ENSRNOG00000019592 |
| drosophila_melanogaster | CG14183 | FBGN0036931 |
| drosophila_melanogaster | CG16789 | FBGN0037712 |
Paralogs (1): IQCA1L (ENSG00000278685)
Protein
Protein identifiers
Dynein regulatory complex subunit 11 — Q86XH1 (reviewed: Q86XH1)
Alternative names: IQ and AAA domain-containing protein 1
All UniProt accessions (3): A0A0A0MSY6, H7BZR5, Q86XH1
UniProt curated annotations — full annotation on UniProt →
Function. Component of the nexin-dynein regulatory complex (N-DRC), a key regulator of ciliary/flagellar motility which maintains the alignment and integrity of the distal axoneme and regulates microtubule sliding in motile axonemes.
Subunit / interactions. Component of the nexin-dynein regulatory complex (N-DRC).
Subcellular location. Cytoplasm. Cytoskeleton. Flagellum axoneme.
Miscellaneous. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay.
Similarity. Belongs to the AAA ATPase family. DRC11 subfamily.
Isoforms (3)
| UniProt ID | Names | Canonical? |
|---|---|---|
| Q86XH1-1 | 1 | yes |
| Q86XH1-2 | 2 | |
| Q86XH1-5 | 3 |
RefSeq proteins (3): NP_001257513, NP_001257514, NP_079002* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR003959 | ATPase_AAA_core | Domain |
| IPR027417 | P-loop_NTPase | Homologous_superfamily |
| IPR052267 | N-DRC_Component | Family |
Pfam: PF00004
UniProt features (19 total): splice variant 4, sequence conflict 4, sequence variant 3, compositionally biased region 3, region of interest 2, chain 1, domain 1, binding site 1
Structure
Experimental structures (PDB)
1 structures.
| PDB | Method | Resolution (Å) |
|---|---|---|
| 8J07 | ELECTRON MICROSCOPY | 4.1 |
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q86XH1-F1 | 79.87 | 0.35 |
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 (1): 575–582
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 0 (showing top):
GO Biological Process (1): microtubule severing (GO:0051013)
GO Molecular Function (4): ATP binding (GO:0005524), microtubule severing ATPase activity (GO:0008568), ATP hydrolysis activity (GO:0016887), nucleotide binding (GO:0000166)
GO Cellular Component (6): nucleus (GO:0005634), cytoplasm (GO:0005737), cytoskeleton (GO:0005856), cilium (GO:0005929), motile cilium (GO:0031514), cell projection (GO:0042995)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| microtubule cytoskeleton organization | 2 |
| ATP-dependent activity | 2 |
| cellular anatomical structure | 2 |
| adenyl ribonucleotide binding | 1 |
| purine ribonucleoside triphosphate binding | 1 |
| polypeptide conformation or assembly isomerase activity | 1 |
| catalytic activity, acting on a protein | 1 |
| microtubule destabilizing activity | 1 |
| ribonucleoside triphosphate phosphatase activity | 1 |
| nucleoside phosphate binding | 1 |
| heterocyclic compound binding | 1 |
| intracellular membrane-bounded organelle | 1 |
| intracellular anatomical structure | 1 |
| intracellular membraneless organelle | 1 |
| intraciliary transport particle | 1 |
| membrane-bounded organelle | 1 |
| plasma membrane bounded cell projection | 1 |
| cilium | 1 |
Protein interactions and networks
STRING
1760 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| DRC11 | DRC5 | Q5JU00 | 668 |
| DRC11 | DRC7 | Q8IY82 | 622 |
| DRC11 | DRC8 | Q5VUJ9 | 578 |
| DRC11 | CCDC149 | Q6ZUS6 | 531 |
| DRC11 | DRC4 | O95995 | 523 |
| DRC11 | LRCOL1 | A6NCL2 | 520 |
| DRC11 | DAW1 | Q8N136 | 518 |
| DRC11 | CALM1 | P02593 | 507 |
| DRC11 | ULK4 | Q96C45 | 502 |
| DRC11 | CALML6 | Q8TD86 | 488 |
| DRC11 | CALML3 | P27482 | 488 |
| DRC11 | CALML5 | Q9NZT1 | 488 |
| DRC11 | CALML4 | Q96GE6 | 488 |
| DRC11 | DRC2 | Q8IXS2 | 486 |
| DRC11 | ADGB | Q8N7X0 | 480 |
IntAct
4 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| KLHL22 | TRAV18 | psi-mi:“MI:0914”(association) | 0.350 |
| FTL | psi-mi:“MI:0914”(association) | 0.350 | |
| ZCCHC10 | ARHGAP10 | psi-mi:“MI:0914”(association) | 0.350 |
BioGRID (5): IQCA1 (Affinity Capture-MS), IQCA1 (Cross-Linking-MS (XL-MS)), ATP5A1 (Cross-Linking-MS (XL-MS)), IQCA1 (Affinity Capture-MS), NEFM (Cross-Linking-MS (XL-MS))
ESM2 similar proteins: A1A5P5, A6H690, A6NCM1, A7SK48, B2RY04, E7EXT2, O70481, P97393, P97564, Q12874, Q13017, Q14185, Q14738, Q1LXZ7, Q24087, Q2KI89, Q2TAA8, Q3SYG4, Q3U0M1, Q45GW3, Q4R8Y5, Q5GJ77, Q5R629, Q5ZL77, Q68F70, Q6AX60, Q6AXQ7, Q6NU25, Q7ZYV9, Q811G0, Q86XH1, Q8BUR4, Q8BWR8, Q8C3J5, Q8CDK3, Q8CIM8, Q8IUC4, Q8IWV7, Q8T773, Q92608
Diamond homologs: A2VDN5, A6H690, A6NCM1, A8IHT2, A8QFF6, A8XV40, B2RYN7, B3M301, B3P8A3, B4G437, B4HGG6, B4JII0, B4K799, B4M0H8, B4NBP4, B4PL32, B4QSF0, B7PXE3, O60058, P40328, Q298L4, Q5HY92, Q5ZK92, Q6AXQ7, Q6AZT2, Q719N1, Q7QBW0, Q86XH1, Q8I0P1, Q9CUL5, Q9ERZ6, Q9QYY8, Q9UBP0, Q6NW58, Q05AS3
SIGNOR signaling
1 interactions.
| A | Effect | B | Mechanism |
|---|---|---|---|
| IQCA1 | “form complex” | “Nexin-dynein regulatory complex” | binding |
Disease & clinical
Clinical variants and AI predictions
ClinVar
89 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 66 |
| Likely benign | 3 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
5450 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 2:236331592:A:G | W714R | 0.996 |
| 2:236331592:A:T | W714R | 0.996 |
| 2:236363925:C:T | G575E | 0.994 |
| 2:236363926:C:A | G575W | 0.993 |
| 2:236363926:C:G | G575R | 0.993 |
| 2:236363926:C:T | G575R | 0.993 |
| 2:236392046:A:G | L448P | 0.992 |
| 2:236497254:C:G | R82P | 0.991 |
| 2:236488124:C:G | R175P | 0.990 |
| 2:236497242:A:G | L86P | 0.990 |
| 2:236363869:C:G | A594P | 0.989 |
| 2:236363890:C:G | A587P | 0.989 |
| 2:236338304:C:A | G679W | 0.988 |
| 2:236344639:G:T | A625D | 0.987 |
| 2:236324780:A:G | W793R | 0.986 |
| 2:236324780:A:T | W793R | 0.986 |
| 2:236363934:A:G | L572P | 0.986 |
| 2:236344640:C:G | A625P | 0.985 |
| 2:236363895:A:T | V585D | 0.984 |
| 2:236338303:C:T | G679E | 0.983 |
| 2:236465526:C:G | R302P | 0.983 |
| 2:236344618:A:T | V632E | 0.982 |
| 2:236344587:G:C | F642L | 0.981 |
| 2:236344587:G:T | F642L | 0.981 |
| 2:236344589:A:G | F642L | 0.981 |
| 2:236338288:G:T | P684H | 0.980 |
| 2:236363925:C:A | G575V | 0.980 |
| 2:236338312:A:G | L676P | 0.979 |
| 2:236338225:G:C | P705R | 0.978 |
| 2:236338304:C:G | G679R | 0.978 |
dbSNP variants (sampled 300 via entrez): RS1000000758 (2:236401732 G>A), RS1000004888 (2:236506175 A>C,G,T), RS1000015202 (2:236312926 C>A), RS1000017138 (2:236453442 C>G), RS1000030593 (2:236402003 A>G), RS1000030912 (2:236375373 C>T), RS1000062105 (2:236352344 G>A), RS1000101127 (2:236498333 C>T), RS1000101711 (2:236442998 C>G,T), RS1000122088 (2:236409617 T>C), RS1000133788 (2:236348021 A>G), RS1000150009 (2:236367660 C>T), RS1000160343 (2:236490807 G>A), RS1000195973 (2:236462603 G>A), RS1000212399 (2:236395693 A>G)
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
1 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST000635_22 | Response to statin therapy | 2.000000e-07 |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
30 total (human), top 30 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Valproic Acid | affects cotreatment, increases expression, affects expression, increases methylation | 7 |
| methylmercuric chloride | decreases expression | 2 |
| methacrylaldehyde | increases abundance, affects cotreatment, decreases expression | 2 |
| Panobinostat | affects cotreatment, increases expression | 2 |
| Acrolein | affects cotreatment, decreases expression, increases abundance | 2 |
| Ozone | decreases expression, increases abundance, affects cotreatment | 2 |
| alpha-pinene | affects cotreatment, decreases expression, increases abundance | 1 |
| bisphenol A | increases expression | 1 |
| trichostatin A | increases expression | 1 |
| sodium arsenite | decreases expression | 1 |
| benzo(e)pyrene | decreases methylation, increases methylation | 1 |
| aflatoxin B2 | decreases methylation | 1 |
| CGP 52608 | affects binding, increases reaction | 1 |
| entinostat | increases expression, affects cotreatment | 1 |
| 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide | increases expression, affects cotreatment | 1 |
| dorsomorphin | affects cotreatment, increases expression | 1 |
| bisphenol S | affects methylation | 1 |
| Sunitinib | decreases expression | 1 |
| Air Pollutants | affects cotreatment, decreases expression, increases abundance | 1 |
| Benzo(a)pyrene | increases methylation | 1 |
| Calcitriol | affects cotreatment, increases expression | 1 |
| Methapyrilene | decreases methylation, increases methylation | 1 |
| Rifampin | decreases expression | 1 |
| Testosterone | affects cotreatment, increases expression, decreases expression | 1 |
| Tobacco Smoke Pollution | decreases expression | 1 |
| Tretinoin | increases expression | 1 |
| Vanadates | decreases expression | 1 |
| 1-Methyl-4-phenylpyridinium | increases expression | 1 |
| Lithium Chloride | increases expression | 1 |
| Volatile Organic Compounds | decreases expression, affects cotreatment | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.