ZDHHC7

gene
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Also known as FLJ10792ZNF370FLJ20279SERZ-BSERZ1DHHC7

Summary

ZDHHC7 (zDHHC palmitoyltransferase 7, HGNC:18459) is a protein-coding gene on chromosome 16q24.1, encoding Palmitoyltransferase ZDHHC7 (Q9NXF8). Golgi-localized palmitoyltransferase that catalyzes the addition of palmitate onto various protein substrates and therefore functions in several unrelated biological processes.

Enables protein-cysteine S-palmitoyltransferase activity. Involved in several processes, including nuclear receptor-mediated steroid hormone signaling pathway; regulation of protein localization; and regulation of signal transduction. Located in Golgi apparatus and nucleoplasm.

Source: NCBI Gene 55625 — RefSeq curated summary.

At a glance

  • GWAS associations: 3
  • Clinical variants (ClinVar): 47 total
  • Druggable target: yes
  • MANE Select transcript: NM_017740

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:18459
Approved symbolZDHHC7
NamezDHHC palmitoyltransferase 7
Location16q24.1
Locus typegene with protein product
StatusApproved
AliasesFLJ10792, ZNF370, FLJ20279, SERZ-B, SERZ1, DHHC7
Ensembl geneENSG00000153786
Ensembl biotypeprotein_coding
OMIM614604
Entrez55625

Gene structure

Transcript identifiers

Ensembl transcripts: 22 — 18 protein_coding, 2 retained_intron, 1 nonsense_mediated_decay, 1 protein_coding_CDS_not_defined

ENST00000313732, ENST00000344861, ENST00000564466, ENST00000564526, ENST00000566909, ENST00000569017, ENST00000569377, ENST00000569488, ENST00000905028, ENST00000905029, ENST00000905030, ENST00000905031, ENST00000905032, ENST00000905033, ENST00000911294, ENST00000911295, ENST00000954815, ENST00000954816, ENST00000954817, ENST00000954818, ENST00000954819, ENST00000954820

RefSeq mRNA: 2 — MANE Select: NM_017740 NM_001145548, NM_017740

CCDS: CCDS10950, CCDS45538

Canonical transcript exons

ENST00000313732 — 8 exons

ExonStartEnd
ENSE000013521748499592284996007
ENSE000013521848501128685011535
ENSE000013761058499030484990635
ENSE000016326558498187084981994
ENSE000019336278497417584976519
ENSE000035865948497792484978005
ENSE000036097468497918984979285
ENSE000036491998497709584977225

Expression profiles

Bgee: expression breadth ubiquitous, 286 present calls, max score 99.13.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 51.7430 / max 291.9827, expressed in 1823 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
15837641.60461821
15837710.13841794

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
secondary oocyteCL:000065599.13gold quality
monocyteCL:000057697.75gold quality
mononuclear cellCL:000084297.74gold quality
leukocyteCL:000073897.63gold quality
pylorusUBERON:000116696.97gold quality
granulocyteCL:000009496.67gold quality
cardia of stomachUBERON:000116296.64gold quality
oocyteCL:000002395.99gold quality
ileal mucosaUBERON:000033195.94gold quality
stromal cell of endometriumCL:000225595.85gold quality
deciduaUBERON:000245095.75gold quality
calcaneal tendonUBERON:000370195.67gold quality
tracheaUBERON:000312695.53gold quality
synovial jointUBERON:000221795.42gold quality
body of tongueUBERON:001187695.32gold quality
renal medullaUBERON:000036295.25gold quality
tongueUBERON:000172394.85gold quality
dorsal root ganglionUBERON:000004494.82gold quality
tibialis anteriorUBERON:000138594.80silver quality
bloodUBERON:000017894.76gold quality
trigeminal ganglionUBERON:000167594.74gold quality
layer of synovial tissueUBERON:000761694.74gold quality
transverse colonUBERON:000115794.58gold quality
urethraUBERON:000005794.48gold quality
pharyngeal mucosaUBERON:000035594.45gold quality
body of stomachUBERON:000116194.43gold quality
saphenous veinUBERON:000731894.41gold quality
superior surface of tongueUBERON:000737194.40gold quality
endocervixUBERON:000045894.33gold quality
skeletal muscle tissue of rectus abdominisUBERON:000451194.30gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes9.60

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

73 targeting ZDHHC7, 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-4262100.0073.263931
HSA-MIR-8485100.0077.574731
HSA-MIR-3163100.0077.238605
HSA-MIR-3925-3P100.0069.951237
HSA-MIR-3613-3P100.0076.367965
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-453199.9969.703181
HSA-MIR-19A-3P99.9875.332762
HSA-MIR-19B-3P99.9875.442754
HSA-MIR-50799.9770.111915
HSA-MIR-146A-5P99.9668.93988
HSA-MIR-146B-5P99.9669.13977
HSA-MIR-55799.9670.011640
HSA-MIR-7153-5P99.9468.891006
HSA-MIR-1236-3P99.9468.041695
HSA-MIR-548AH-3P99.9372.544872
HSA-MIR-548AM-3P99.9372.544872
HSA-MIR-345-3P99.8970.231421
HSA-MIR-548E-5P99.8972.734486
HSA-MIR-467999.7669.191229
HSA-MIR-148A-3P99.7473.771700
HSA-MIR-148B-3P99.7473.751700
HSA-MIR-152-3P99.7473.751703
HSA-MIR-674599.7465.331321
HSA-MIR-120899.7068.281533
HSA-MIR-377-5P99.7065.28712
HSA-MIR-608699.7065.38699

Literature-anchored findings (GeneRIF, showing 6)

  • the DHHC-7 and -21 proteins are novel targets to selectively inhibit membrane sex steroid receptor localization and function (PMID:22031296)
  • DHHC7-mediated palmitoylation of Fas allows a proper Fas expression level by preventing its degradation through the lysosomes. (PMID:25301068)
  • The ZDHHC7-mediated SCRIB palmitoylation is critical for SCRIB membrane targeting, cell polarity and tumor suppression, providing new mechanistic insights of how dynamic protein palmitoylation regulates cell polarity and tumorigenesis. (PMID:27380321)
  • identified DHHC7 as a JAM-C palmitoylating enzyme (PMID:28196865)
  • demonstrated the importance of Zdhhc7 for assembling proper brain structure, function, and behavior on a system level in mice in a sex-related manner (PMID:31183559)
  • Palmitoyl acyltransferase ZDHHC7 inhibits androgen receptor and suppresses prostate cancer. (PMID:37198397)

Cross-species orthologs

12 orthologs

OrganismSymbolGene ID
danio_reriozdhhc7ENSDARG00000019484
mus_musculusZdhhc7ENSMUSG00000031823
rattus_norvegicusZdhhc7ENSRNOG00000017342
drosophila_melanogasterDnz1FBGN0027453
drosophila_melanogasterCG1407FBGN0033474
drosophila_melanogasterCG17287FBGN0034202
caenorhabditis_elegansdhhc-7WBGENE00007637
caenorhabditis_elegansdhhc-12WBGENE00010323
caenorhabditis_elegansdhhc-2WBGENE00012948
caenorhabditis_elegansWBGENE00014075
caenorhabditis_elegansWBGENE00016620
caenorhabditis_elegansWBGENE00020066

Paralogs (17): ZDHHC6 (ENSG00000023041), ZDHHC15 (ENSG00000102383), ZDHHC2 (ENSG00000104219), ZDHHC4 (ENSG00000136247), ZDHHC1 (ENSG00000159714), ZDHHC12 (ENSG00000160446), ZDHHC3 (ENSG00000163812), ZDHHC19 (ENSG00000163958), ZDHHC14 (ENSG00000175048), ZDHHC21 (ENSG00000175893), ZDHHC22 (ENSG00000177108), ZDHHC20 (ENSG00000180776), ZDHHC23 (ENSG00000184307), ZDHHC9 (ENSG00000188706), ZDHHC11 (ENSG00000188818), ZDHHC18 (ENSG00000204160), ZDHHC11B (ENSG00000206077)

Protein

Protein identifiers

Palmitoyltransferase ZDHHC7Q9NXF8 (reviewed: Q9NXF8)

Alternative names: Acyltransferase ZDHHC7, Zinc finger DHHC domain-containing protein 7

All UniProt accessions (3): Q9NXF8, H3BMI0, H3BNQ9

UniProt curated annotations — full annotation on UniProt →

Function. Golgi-localized palmitoyltransferase that catalyzes the addition of palmitate onto various protein substrates and therefore functions in several unrelated biological processes. Has no stringent fatty acid selectivity and in addition to palmitate can also transfer onto target proteins myristate from tetradecanoyl-CoA and stearate from octadecanoyl-CoA. Palmitoylates sex steroid hormone receptors, including ESR1, PGR and AR, thereby regulating their targeting to the plasma membrane and their function in rapid intracellular signaling upon binding of sex hormones. Palmitoylates GNAQ, a heterotrimeric G protein, regulating its dynamic localization at the plasma membrane and is thereby involved in GNAQ-dependent G protein-coupled receptor signaling pathways. Also functions in ligand-induced cell death by regulating the FAS signaling pathway through the palmitoylation and stabilization of the receptor at the plasma membrane. In epithelial cells, palmitoylates SCRIB and regulates its localization to the plasma membrane, regulating indirectly cell polarity and differentiation. Also palmitoylates JAM3 and promotes its expression at tight junctions and regulates its function in cell migration. Palmitoylates the glucose transporter GLUT4/SLC2A4 and controls the insulin-dependent translocation of GLUT4 to the plasma membrane. In brain, could also palmitoylate SNAP25 and DLG4/PSD95. Could also palmitoylate DNAJC5 and regulate its localization to the Golgi membrane. Could also palmitoylate NCDN. May play a role in follicle stimulation hormone (FSH) activation of testicular Sertoli cells. Activates pyroptosis by catalyzing palmitoylation of gasdermin-D (GSDMD).

Subunit / interactions. Homooligomers. Heterooligomers with ZDHHC3.

Subcellular location. Golgi apparatus membrane.

Post-translational modifications. Autopalmitoylated.

Domain organisation. The DHHC domain is required for palmitoyltransferase activity.

Similarity. Belongs to the DHHC palmitoyltransferase family.

Isoforms (2)

UniProt IDNamesCanonical?
Q9NXF8-11yes
Q9NXF8-22

RefSeq proteins (2): NP_001139020, NP_060210* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001594Palmitoyltrfase_DHHCDomain
IPR039859PFA4/ZDH16/20/ERF2-likeFamily

Pfam: PF01529

Catalyzed reactions (Rhea), 3 shown:

  • L-cysteinyl-[protein] + hexadecanoyl-CoA = S-hexadecanoyl-L-cysteinyl-[protein] + CoA (RHEA:36683)
  • L-cysteinyl-[protein] + tetradecanoyl-CoA = S-tetradecanoyl-L-cysteinyl-[protein] + CoA (RHEA:59736)
  • L-cysteinyl-[protein] + octadecanoyl-CoA = S-octadecanoyl-L-cysteinyl-[protein] + CoA (RHEA:59740)

UniProt features (16 total): topological domain 5, transmembrane region 4, sequence variant 2, chain 1, domain 1, active site 1, splice variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9NXF8-F183.850.65

Functional residue map

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

Catalytic / active sites (1): 160 (s-palmitoyl cysteine intermediate)

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-9009391Extra-nuclear estrogen signaling

MSigDB gene sets: 233 (showing top): GSE18804_SPLEEN_MACROPHAGE_VS_BRAIN_TUMORAL_MACROPHAGE_DN, GOBP_MORPHOGENESIS_OF_AN_EPITHELIUM, GOBP_RESPONSE_TO_NITROGEN_COMPOUND, GOBP_CARBOHYDRATE_TRANSPORT, GOBP_EPITHELIUM_DEVELOPMENT, GOBP_CELLULAR_RESPONSE_TO_LIPID, GOBP_LIPOPROTEIN_METABOLIC_PROCESS, GOBP_PROTEIN_TARGETING, GOBP_CELLULAR_RESPONSE_TO_OXYGEN_CONTAINING_COMPOUND, GOBP_PEPTIDYL_CYSTEINE_MODIFICATION, GOBP_PROTEIN_LOCALIZATION_TO_CELL_PERIPHERY, GOBP_POSITIVE_REGULATION_OF_TRANSMEMBRANE_TRANSPORT, GOBP_CELLULAR_RESPONSE_TO_INSULIN_STIMULUS, GOBP_HORMONE_MEDIATED_SIGNALING_PATHWAY, GOBP_PROTEIN_TARGETING_TO_MEMBRANE

GO Biological Process (17): protein targeting to membrane (GO:0006612), regulation of G protein-coupled receptor signaling pathway (GO:0008277), negative regulation of catabolic process (GO:0009895), positive regulation of D-glucose transmembrane transport (GO:0010828), peptidyl-L-cysteine S-palmitoylation (GO:0018230), protein palmitoylation (GO:0018345), androgen receptor signaling pathway (GO:0030521), polarized epithelial cell differentiation (GO:0030859), steroid hormone receptor signaling pathway (GO:0043401), glucose import in response to insulin stimulus (GO:0044381), progesterone receptor signaling pathway (GO:0050847), protein localization to plasma membrane (GO:0072659), regulation of protein localization to cell-cell junction (GO:0150106), regulation of Fas signaling pathway (GO:1902044), regulation of protein localization to plasma membrane (GO:1903076), positive regulation of epithelial to mesenchymal transition (GO:0010718), D-glucose transmembrane transport (GO:1904659)

GO Molecular Function (7): palmitoyltransferase activity (GO:0016409), protein-cysteine S-myristoyltransferase activity (GO:0019705), protein-cysteine S-palmitoyltransferase activity (GO:0019706), protein-cysteine S-stearoyltransferase activity (GO:0140439), protein binding (GO:0005515), transferase activity (GO:0016740), acyltransferase activity (GO:0016746)

GO Cellular Component (5): Golgi membrane (GO:0000139), nucleoplasm (GO:0005654), endoplasmic reticulum (GO:0005783), Golgi apparatus (GO:0005794), membrane (GO:0016020)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
ESR-mediated signaling1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
protein-cysteine S-acyltransferase activity3
regulation of signal transduction2
nuclear receptor-mediated steroid hormone signaling pathway2
cellular anatomical structure2
cytoplasm2
endomembrane system2
intracellular membrane-bounded organelle2
protein targeting1
establishment of protein localization to membrane1
G protein-coupled receptor signaling pathway1
catabolic process1
negative regulation of metabolic process1
regulation of catabolic process1
regulation of D-glucose transmembrane transport1
positive regulation of transmembrane transport1
D-glucose transmembrane transport1
peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine1
protein palmitoylation1
protein lipidation1
protein acylation1
morphogenesis of a polarized epithelium1
epithelial cell differentiation1
hormone-mediated signaling pathway1
cellular response to steroid hormone stimulus1
cellular response to insulin stimulus1
D-glucose import across plasma membrane1
protein localization to membrane1
protein localization to cell periphery1
regulation of protein localization1
protein localization to cell-cell junction1
Fas signaling pathway1
protein localization to plasma membrane1
regulation of protein localization to cell periphery1
regulation of protein localization to membrane1
epithelial to mesenchymal transition1
regulation of epithelial to mesenchymal transition1
positive regulation of cell differentiation1
positive regulation of multicellular organismal process1
hexose transmembrane transport1
acyltransferase activity, transferring groups other than amino-acyl groups1

Protein interactions and networks

STRING

712 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZDHHC7LYPLA2O95372597
ZDHHC7ABHD17AQ96GS6515
ZDHHC7PPT1P50897506
ZDHHC7PPT2Q9UMR5485
ZDHHC7ZDHHC8Q9ULC8483
ZDHHC7ZDHHC17Q8IUH5451
ZDHHC7ZDHHC13Q8IUH4446
ZDHHC7ABHD17BQ5VST6434
ZDHHC7SDR42E1Q8WUS8425
ZDHHC7LYPLA1O75608423
ZDHHC7ZDHHC3Q9NYG2422
ZDHHC7GOLGA7Q7Z5G4420
ZDHHC7ABHD17CQ6PCB6417
ZDHHC7ZDHHC14Q8IZN3413
ZDHHC7ZDHHC5Q9C0B5407

IntAct

38 interactions, top by confidence:

ABTypeScore
ZDHHC7psi-mi:“MI:0915”(physical association)0.370
CCL1ZDHHC7psi-mi:“MI:0915”(physical association)0.370
CCL2ZDHHC7psi-mi:“MI:0915”(physical association)0.370
CCL22ZDHHC7psi-mi:“MI:0915”(physical association)0.370
CCL3L1ZDHHC7psi-mi:“MI:0915”(physical association)0.370
CCL8ZDHHC7psi-mi:“MI:0915”(physical association)0.370
IFNL1ZDHHC7psi-mi:“MI:0915”(physical association)0.370
IFNL4ZDHHC7psi-mi:“MI:0915”(physical association)0.370
IL17AZDHHC7psi-mi:“MI:0915”(physical association)0.370
IL18ZDHHC7psi-mi:“MI:0915”(physical association)0.370
IL31ZDHHC7psi-mi:“MI:0915”(physical association)0.370
LTAZDHHC7psi-mi:“MI:0915”(physical association)0.370
PF4V1ZDHHC7psi-mi:“MI:0915”(physical association)0.370

BioGRID (32): ZDHHC7 (Affinity Capture-RNA), ZDHHC7 (Affinity Capture-RNA), CKM (Affinity Capture-MS), TMEM259 (Affinity Capture-MS), REEP5 (Affinity Capture-MS), NDFIP1 (Affinity Capture-MS), TMEM186 (Affinity Capture-MS), MARCH6 (Affinity Capture-MS), CKM (Affinity Capture-MS), MARCH6 (Affinity Capture-MS), TMEM186 (Affinity Capture-MS), NDFIP1 (Affinity Capture-MS), ZDHHC7 (Affinity Capture-RNA), ZDHHC7 (Two-hybrid), ZDHHC7 (Two-hybrid)

ESM2 similar proteins: A0A087WTH1, A0A125YWU9, A0PK84, A6PVL3, C9JQL5, F1QHM7, F1QX91, O15503, O41933, O70418, O88728, P0DI73, P13164, P26376, Q01628, Q01629, Q08755, Q0II74, Q21642, Q32L65, Q3UNB8, Q3YBM2, Q5FVR1, Q5FWL7, Q5I0I2, Q5R8D6, Q5RF75, Q5Y5T3, Q6DHI1, Q76IC6, Q7M734, Q7TQJ1, Q8BGI3, Q8CES1, Q8CFA6, Q8IYP9, Q8N6L7, Q8WVZ1, Q91WU6, Q921C1

Diamond homologs: A0A0R4IDP3, A2CEX1, A2VEY9, A5WVX9, B3DN87, C8VCL4, E1BLT8, E7F021, E7F587, E7FBS9, E7FH11, E9PTT0, E9QCD3, F1Q7H8, F1QAM1, F1QHM7, F1QX91, F1QXD3, F1R013, F1RE57, J9VJ99, O60069, O74384, O80685, P42836, P59267, P59268, Q04629, Q0VC89, Q10L01, Q2TGJ1, Q2TGJ4, Q2TGK3, Q2THW7, Q2THW8, Q2THW9, Q2THX0, Q2THX1, Q4R690, Q4WZL8

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 21 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

GO biological processes:

GO termPartnersFoldFDR
chemokine-mediated signaling pathway585.3×2e-07
antimicrobial humoral immune response mediated by antimicrobial peptide651.2×2e-07
positive regulation of cell migration619.5×1e-05
cell-cell signaling518.3×2e-04
inflammatory response815.9×6e-07

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance39
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1932 predictions. Top by Δscore:

VariantEffectΔscore
16:84977089:GCTT:Gdonor_loss1.0000
16:84977090:CTTAC:Cdonor_loss1.0000
16:84977091:TTACC:Tdonor_loss1.0000
16:84977094:C:CTdonor_loss1.0000
16:84978003:CAT:Cacceptor_gain1.0000
16:84979183:ACTT:Adonor_loss1.0000
16:84979184:CTT:Cdonor_loss1.0000
16:84979185:TT:Tdonor_loss1.0000
16:84979187:A:ACdonor_gain1.0000
16:84979187:A:Tdonor_loss1.0000
16:84979188:C:CAdonor_gain1.0000
16:84979188:CA:Cdonor_gain1.0000
16:84979188:CAG:Cdonor_gain1.0000
16:84979188:CAGT:Cdonor_gain1.0000
16:84979188:CAGTG:Cdonor_gain1.0000
16:84979281:AAATA:Aacceptor_gain1.0000
16:84979282:AATA:Aacceptor_gain1.0000
16:84979283:ATA:Aacceptor_gain1.0000
16:84979283:ATAC:Aacceptor_loss1.0000
16:84979284:TA:Tacceptor_gain1.0000
16:84979285:AC:Aacceptor_loss1.0000
16:84979286:C:CCacceptor_gain1.0000
16:84979286:CTGAA:Cacceptor_loss1.0000
16:84981867:TACCT:Tdonor_loss1.0000
16:84981868:AC:Adonor_loss1.0000
16:84981869:C:CTdonor_loss1.0000
16:84981991:CCCC:Cacceptor_gain1.0000
16:84981992:CCCC:Cacceptor_gain1.0000
16:84981993:CC:Cacceptor_gain1.0000
16:84981993:CCCT:Cacceptor_loss1.0000

AlphaMissense

2020 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:84979201:A:CF175L1.000
16:84979201:A:TF175L1.000
16:84979203:A:GF175L1.000
16:84979223:C:AG168V1.000
16:84979223:C:TG168E1.000
16:84979228:A:CC166W1.000
16:84979229:C:TC166Y1.000
16:84979230:A:GC166R1.000
16:84979231:A:CN165K1.000
16:84979231:A:TN165K1.000
16:84979234:G:CN164K1.000
16:84979234:G:TN164K1.000
16:84979242:A:GW162R1.000
16:84979242:A:TW162R1.000
16:84979246:G:CC160W1.000
16:84979247:C:GC160S1.000
16:84979247:C:TC160Y1.000
16:84979248:A:GC160R1.000
16:84979248:A:TC160S1.000
16:84979249:G:CH159Q1.000
16:84979249:G:TH159Q1.000
16:84979251:G:CH159D1.000
16:84979251:G:TH159N1.000
16:84979252:A:CH158Q1.000
16:84979252:A:TH158Q1.000
16:84979253:T:AH158L1.000
16:84979254:G:CH158D1.000
16:84979254:G:TH158N1.000
16:84979255:A:CD157E1.000
16:84979255:A:TD157E1.000

dbSNP variants (sampled 300 via entrez): RS1000044375 (16:85011854 G>A), RS1000132206 (16:84998927 G>A,C), RS1000239549 (16:84995085 C>A,G), RS1000243452 (16:85015588 C>T), RS1000393313 (16:85019884 C>G,T), RS1000418835 (16:85000171 C>T), RS1000467133 (16:84990737 G>A,C,T), RS1000468272 (16:85019497 C>A,T), RS1000472241 (16:85027522 C>T), RS1000550247 (16:85004207 C>T), RS1000561113 (16:85024261 T>C), RS1000566693 (16:84996631 A>C,G), RS1000662508 (16:85000230 G>A,C), RS1000663401 (16:85028713 C>G,T), RS1000732809 (16:85000047 G>A)

Disease associations

OMIM: gene MIM:614604 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

3 associations (top):

StudyTraitp-value
GCST000175_24Height8.000000e-07
GCST002647_117Height5.000000e-10
GCST008507_2Stress sensitivity (neuroticism score x major depressive disorder status interaction)2.000000e-06

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0007660neuroticism measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: yes

ChEMBL targets (1): CHEMBL6066246 (SINGLE PROTEIN)

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

PharmGKB clinical annotations

1 annotations.

VariantTypeLevelDrugsPhenotypes
rs3210967Efficacy3methylphenidateAttention Deficit Disorder with Hyperactivity

PharmGKB variants

1 variants.

VariantGenesLevelScore#Clin annotsDrugs
rs3210967ZDHHC730.001methylphenidate

ChEMBL bioactivities

1 potent at pChembl≥5 of 2 total, top 1 by pChembl (potency: 10 = 0.1 nM, 6 = 1 µM).

pChemblTypeValueUnitMolecule
5.36IC504400nMCHEMBL5567020

PubChem BioAssay actives

1 with measured affinity, of 2 total; 1 most potent distinct compounds. Largely complementary to BindingDB; screening values are coarse (µM, 4 dp), so sub-nM hits tie at the floor.

CompoundAssayTypeValueUnit
S-(2-acetamidoethyl) 2-bromohexadecanethioate2084115: Inhibition of ZDHHC7 (unknown origin)ic504.4000uM

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
Valproic Acidincreases expression, increases methylation, affects cotreatment3
Resveratrolaffects cotreatment, decreases expression, increases expression2
Arsenicaffects methylation, decreases expression, increases abundance2
Estradioldecreases expression2
aristolochic acid Idecreases expression1
triphenyl phosphateaffects expression1
bisphenol Adecreases methylation1
beta-lapachoneincreases expression1
sodium arseniteincreases abundance, decreases expression1
2,3-bis(3’-hydroxybenzyl)butyrolactoneaffects cotreatment, decreases expression1
perfluorooctane sulfonic aciddecreases expression1
Temozolomidedecreases expression1
Air Pollutantsaffects expression, increases abundance1
Benzo(a)pyreneaffects methylation1
Caffeinedecreases phosphorylation1
Coumestrolaffects cotreatment, decreases expression1
Hydralazineaffects cotreatment, increases expression1
Ozoneaffects expression, increases abundance1
Plant Extractsaffects cotreatment, increases expression1
Smokeincreases expression1
Thiramdecreases expression1
Tretinoinincreases expression1
Urethaneincreases expression1
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxidedecreases expression1
Aflatoxin B1decreases methylation1
Cadmium Chloridedecreases expression1

ChEMBL screening assays

1 unique, capped per target: 1 binding

Representative assays (with source publication via chembl_document):

Assay IDTypeDescriptionSource paper
CHEMBL5524588BindingInhibition of ZDHHC7 (unknown origin)Modulators for palmitoylation of proteins and small molecules. — Eur J Med Chem

Cellosaurus cell lines

3 cell lines: 3 cancer cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_B2LQAbcam HeLa ZDHHC7 KOCancer cell lineFemale
CVCL_TZ04HAP1 ZDHHC7 (-) 1Cancer cell lineMale
CVCL_TZ05HAP1 ZDHHC7 (-) 2Cancer cell lineMale

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.