ZNF415

gene
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Summary

ZNF415 (zinc finger protein 415, HGNC:20636) is a protein-coding gene on chromosome 19q13.42, encoding Zinc finger protein 415 (Q09FC8). Involved in transcriptional regulation.

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in fibrillar center and microtubule cytoskeleton.

Source: NCBI Gene 55786 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 103 total
  • MANE Select transcript: NM_018355

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:20636
Approved symbolZNF415
Namezinc finger protein 415
Location19q13.42
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000170954
Ensembl biotypeprotein_coding
OMIM619506
Entrez55786

Gene structure

Transcript identifiers

Ensembl transcripts: 31 — 20 protein_coding, 6 protein_coding_CDS_not_defined, 4 nonsense_mediated_decay, 1 retained_intron

ENST00000243643, ENST00000421033, ENST00000500065, ENST00000594011, ENST00000594286, ENST00000595174, ENST00000595193, ENST00000595359, ENST00000595813, ENST00000596051, ENST00000596106, ENST00000596683, ENST00000597503, ENST00000597748, ENST00000597877, ENST00000598024, ENST00000598578, ENST00000599261, ENST00000600098, ENST00000600120, ENST00000600574, ENST00000601110, ENST00000601215, ENST00000601493, ENST00000602024, ENST00000602110, ENST00000882509, ENST00000882510, ENST00000937691, ENST00000937692, ENST00000937693

RefSeq mRNA: 26 — MANE Select: NM_018355 NM_001136038, NM_001164309, NM_001330759, NM_001330766, NM_001352130, NM_001352131, NM_001352132, NM_001352133, NM_001352134, NM_001352135, NM_001352136, NM_001352137, NM_001352138, NM_001352139, NM_001352140, NM_001352141, NM_001352142, NM_001352143, NM_001352144, NM_001352146, NM_001352147, NM_001352148, NM_001352149, NM_001352150, NM_001352151, NM_018355

CCDS: CCDS12860, CCDS54313, CCDS82393

Canonical transcript exons

ENST00000243643 — 4 exons

ExonStartEnd
ENSE000035108365312266253122743
ENSE000035836945310787953109908
ENSE000037331785311631353116433
ENSE000039214625313285653132910

Expression profiles

Bgee: expression breadth ubiquitous, 261 present calls, max score 95.22.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 3.9561 / max 110.6103, expressed in 924 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1825533.9359924
1825520.01463
1825510.00563

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
spermCL:000001995.22gold quality
male germ cellCL:000001593.40gold quality
adrenal tissueUBERON:001830392.21gold quality
cortical plateUBERON:000534390.64gold quality
right adrenal gland cortexUBERON:003582789.09gold quality
right adrenal glandUBERON:000123388.90gold quality
left adrenal glandUBERON:000123488.72gold quality
right testisUBERON:000453488.59gold quality
left testisUBERON:000453388.53gold quality
left adrenal gland cortexUBERON:003582588.49gold quality
cerebellar hemisphereUBERON:000224588.20gold quality
cerebellar cortexUBERON:000212988.13gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099187.90gold quality
right hemisphere of cerebellumUBERON:001489087.81gold quality
adrenal glandUBERON:000236987.68gold quality
adrenal cortexUBERON:000123587.59gold quality
testisUBERON:000047387.57gold quality
C1 segment of cervical spinal cordUBERON:000646986.82gold quality
cerebellumUBERON:000203786.60gold quality
prefrontal cortexUBERON:000045185.69gold quality
ganglionic eminenceUBERON:000402385.64gold quality
Brodmann (1909) area 9UBERON:001354085.22gold quality
right frontal lobeUBERON:000281085.20gold quality
spinal cordUBERON:000224084.96gold quality
corpus callosumUBERON:000233684.76gold quality
right atrium auricular regionUBERON:000663184.34gold quality
heart left ventricleUBERON:000208484.20gold quality
amygdalaUBERON:000187684.06gold quality
putamenUBERON:000187484.03gold quality
dorsolateral prefrontal cortexUBERON:000983483.96gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no4.06

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

40 targeting ZNF415, 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-6833-3P100.0070.633197
HSA-MIR-4768-5P100.0069.492861
HSA-MIR-3064-3P100.0070.091254
HSA-MIR-6873-3P100.0071.422626
HSA-MIR-1277-5P100.0073.955056
HSA-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-98-3P100.0074.083907
HSA-MIR-5011-5P100.0083.465820
HSA-MIR-7110-3P100.0073.182486
HSA-MIR-511-3P99.9968.851467
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
HSA-MIR-3617-3P99.9867.86918
HSA-MIR-302C-5P99.9772.563642
HSA-MIR-6809-3P99.9171.453814
HSA-MIR-6817-3P99.7968.352126
HSA-MIR-451799.7669.191867
HSA-MIR-46699.6770.852863
HSA-MIR-449999.6267.291470
HSA-MIR-582-5P99.4770.792635
HSA-MIR-6739-3P99.2268.841843
HSA-MIR-4764-5P98.8865.53894
HSA-MIR-443998.5367.53793
HSA-MIR-3136-5P98.5367.68793
HSA-MIR-807898.3265.73361
HSA-MIR-6818-5P97.5067.101167
HSA-MIR-96-3P97.4768.03839
HSA-MIR-4433B-3P97.2263.62663

Literature-anchored findings (GeneRIF, showing 2)

  • ZNF415 isoforms in COS-7 cells inhibits the transcriptional activities of AP-1 and p53, suggesting that the ZNF415 protein may be involved in AP-1- and p53-mediated transcriptional activity. (PMID:17055453)
  • ZfLp is a zinc finger protein that functions as a drug carrier protein. (PMID:22863851)

Cross-species orthologs

0 orthologs

Paralogs (176): ZNF195 (ENSG00000005801), ZNF112 (ENSG00000062370), ZNF275 (ENSG00000063587), ZNF37A (ENSG00000075407), ZNF510 (ENSG00000081386), ZNF506 (ENSG00000081665), ZNF268 (ENSG00000090612), MZF1 (ENSG00000099326), ZNF629 (ENSG00000102870), ZNF175 (ENSG00000105497), ZNF85 (ENSG00000105750), ZFP30 (ENSG00000120784), ZNF45 (ENSG00000124459), ZNF391 (ENSG00000124613), ZNF436 (ENSG00000125945), ZNF484 (ENSG00000127081), ZNF835 (ENSG00000127903), ZNF780B (ENSG00000128000), ZSCAN10 (ENSG00000130182), ZNF317 (ENSG00000130803), ZNF331 (ENSG00000130844), ZNF227 (ENSG00000131115), ZNF141 (ENSG00000131127), ZNF132 (ENSG00000131849), ZNF189 (ENSG00000136870), ZIM3 (ENSG00000141946), ZFP14 (ENSG00000142065), ZNF514 (ENSG00000144026), ZNF300 (ENSG00000145908), RBAK (ENSG00000146587), ZNF157 (ENSG00000147117), ZNF182 (ENSG00000147118), ZNF41 (ENSG00000147124), ZNF7 (ENSG00000147789), ZNF117 (ENSG00000152926), ZNF221 (ENSG00000159905), ZNF235 (ENSG00000159917), ZNF714 (ENSG00000160352), ZNF577 (ENSG00000161551), ZNF12 (ENSG00000164631)

Protein

Protein identifiers

Zinc finger protein 415Q09FC8 (reviewed: Q09FC8)

All UniProt accessions (12): Q09FC8, M0QX59, M0QXZ4, M0QZ38, M0QZA6, M0R0D9, M0R0R1, M0R191, M0R1N1, M0R2I1, M0R2T6, M0R358

UniProt curated annotations — full annotation on UniProt →

Function. Involved in transcriptional regulation. Transcriptional activity differed among the various isoforms. All isoforms except isoform 3 seem to suppresses the transcriptional activities of AP-1 and p53/TP53.

Subcellular location. Nucleus. Cytoplasm.

Tissue specificity. Expressed in all tissues examined. Isoforms are differentially expressed. Isoform 3 and isoform 5 were highly expressed, isoform 4 moderately expressed, isoform 2 lower expression, the lowest expression level was seem with isoform 1.

Isoforms (6)

UniProt IDNamesCanonical?
Q09FC8-11, ZNF415-3yes
Q09FC8-22, ZNF415-2
Q09FC8-33, ZNF415-1
Q09FC8-44, ZNF415-4
Q09FC8-55, ZNF415-5
Q09FC8-66

RefSeq proteins (26): NP_001129510, NP_001157781, NP_001317688, NP_001317695, NP_001339059, NP_001339060, NP_001339061, NP_001339062, NP_001339063, NP_001339064, NP_001339065, NP_001339066, NP_001339067, NP_001339068, NP_001339069, NP_001339070, NP_001339071, NP_001339072, NP_001339073, NP_001339075, NP_001339076, NP_001339077, NP_001339078, NP_001339079, NP_001339080, NP_060825* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR013087Znf_C2H2_typeDomain
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096

UniProt features (23 total): zinc finger region 12, splice variant 5, sequence variant 5, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q09FC8-F158.950.23

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 56 (showing top): GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_MCMV_INFECTION_DN, BERENJENO_TRANSFORMED_BY_RHOA_UP, MARSON_BOUND_BY_E2F4_UNSTIMULATED, JAIN_NFKB_SIGNALING, GOCC_NUCLEOLUS, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, MIKKELSEN_ES_ICP_WITH_H3K4ME3, PEDRIOLI_MIR31_TARGETS_DN, ROESSLER_LIVER_CANCER_METASTASIS_DN, ONKEN_UVEAL_MELANOMA_DN, ZWANG_TRANSIENTLY_UP_BY_2ND_EGF_PULSE_ONLY, P53_DN.V1_UP, PIEPOLI_LGI1_TARGETS_DN, SHEN_SMARCA2_TARGETS_UP, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY

GO Biological Process (2): regulation of transcription by RNA polymerase II (GO:0006357), regulation of DNA-templated transcription (GO:0006355)

GO Molecular Function (6): RNA polymerase II cis-regulatory region sequence-specific DNA binding (GO:0000978), DNA-binding transcription factor activity, RNA polymerase II-specific (GO:0000981), zinc ion binding (GO:0008270), DNA binding (GO:0003677), protein binding (GO:0005515), metal ion binding (GO:0046872)

GO Cellular Component (5): fibrillar center (GO:0001650), nucleus (GO:0005634), cytoplasm (GO:0005737), microtubule cytoskeleton (GO:0015630), nucleolus (GO:0005730)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
RNA Polymerase II Transcription1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
RNA polymerase II transcription regulatory region sequence-specific DNA binding2
cellular anatomical structure2
regulation of DNA-templated transcription1
transcription by RNA polymerase II1
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
cis-regulatory region sequence-specific DNA binding1
chromatin1
DNA-binding transcription factor activity1
regulation of transcription by RNA polymerase II1
transition metal ion binding1
nucleic acid binding1
binding1
cation binding1
nucleolus1
intracellular membrane-bounded organelle1
intracellular anatomical structure1
cytoskeleton1
nuclear lumen1
intracellular membraneless organelle1

Protein interactions and networks

STRING

376 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF415ANHXE9PGG2419
ZNF415LRATD1Q96KN4396
ZNF415CALHM2Q9HA72389
ZNF415MDFIQ99750356
ZNF415LRRC70Q7Z2Q7348
ZNF415ELOVL4Q9GZR5311
ZNF415NBPF20P0DPF2302
ZNF415CCDC59Q9P031296
ZNF415CNTNAP2Q9UHC6288
ZNF415RNF141Q8WVD5272
ZNF415TMEM25Q86YD3270
ZNF415KRT37O76014258
ZNF415KRT38O76015252
ZNF415ABHD3Q8WU67252
ZNF415SOX14O95416252

IntAct

8 interactions, top by confidence:

ABTypeScore
MTUS2ZNF415psi-mi:“MI:0915”(physical association)0.560
KRTAP4-12ZNF415psi-mi:“MI:0915”(physical association)0.560
ZNF415KRTAP4-12psi-mi:“MI:0915”(physical association)0.560
ZNF415MTUS2psi-mi:“MI:0915”(physical association)0.560
Mpsi-mi:“MI:0914”(association)0.350

BioGRID (8): ZNF415 (Two-hybrid), KRTAP4-12 (Two-hybrid), ZNF415 (Synthetic Lethality), ZNF415 (Two-hybrid), ZNF415 (Affinity Capture-MS), ZNF415 (Negative Genetic), ZNF415 (Reconstituted Complex), ZNF415 (Two-hybrid)

ESM2 similar proteins: A0A087WUV0, A0JNB1, A2VDP4, B2RUI1, P0CG31, P10072, P17025, P17036, P17097, P18733, P51814, Q08ER8, Q09FC8, Q0VGE8, Q14590, Q15937, Q16600, Q2M3X9, Q4V8A8, Q5CZA5, Q5R8G9, Q5RBX0, Q5VIY5, Q68DI1, Q6J6I6, Q6NX49, Q6P1L6, Q6PG37, Q6ZMS4, Q6ZMW2, Q80YP6, Q86UD4, Q86Y25, Q8IZ26, Q8N184, Q8NB42, Q8NEK5, Q8TAF7, Q8TF47, Q8WXB4

Diamond homologs: A0A096LPI5, A6NIU2, A6NJG6, F2Z398, P0DTE4, P51957, Q09FC8, Q5H9K5, Q5T7P6, Q68CZ1, Q6B4Z3, Q6UX73, Q86U02, Q8IV13, Q8N7M2, Q8N9N2, Q8NDZ0, Q8NEM8, Q8TDM0, Q92918, Q96J02, Q96MD7, Q9BUA6, Q9NXG0, A0A1W2PQL4, A2RRD8, A2VDQ7, A6NHJ4, A6NK75, A6NN14, A6NNF4, A6NP11, B4DX44, B4DXR9, E9PW05, O14628, O43345, O75290, O75346, O75373

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance88
Likely benign5
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1027 predictions. Top by Δscore:

VariantEffectΔscore
19:53109904:CAGAT:Cacceptor_gain1.0000
19:53109905:AGAT:Aacceptor_gain1.0000
19:53109906:GAT:Gacceptor_gain1.0000
19:53109907:AT:Aacceptor_gain1.0000
19:53109907:ATCTA:Aacceptor_loss1.0000
19:53109908:TC:Tacceptor_loss1.0000
19:53109909:C:CCacceptor_gain1.0000
19:53109909:C:Tacceptor_loss1.0000
19:53109911:A:Cacceptor_gain1.0000
19:53109918:A:ACacceptor_gain1.0000
19:53109918:A:Cacceptor_gain1.0000
19:53116439:C:CTacceptor_gain1.0000
19:53116439:C:Tacceptor_gain1.0000
19:53109910:T:Cacceptor_loss0.9900
19:53109911:A:ACacceptor_gain0.9900
19:53116434:C:CCacceptor_gain0.9900
19:53116440:G:Cacceptor_gain0.9900
19:53122742:TG:Tacceptor_gain0.9900
19:53122744:C:CCacceptor_gain0.9900
19:53132855:CG:Cdonor_gain0.9900
19:53116431:CAA:Cacceptor_gain0.9800
19:53116440:G:GCacceptor_gain0.9800
19:53122739:CAATG:Cacceptor_gain0.9800
19:53132854:A:ACdonor_gain0.9800
19:53132855:C:CCdonor_gain0.9800
19:53109907:ATCT:Aacceptor_gain0.9700
19:53109908:TCTA:Tacceptor_gain0.9700
19:53116311:AC:Adonor_gain0.9700
19:53116312:CC:Cdonor_gain0.9700
19:53116352:C:Adonor_gain0.9700

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000156017 (19:53121936 G>C), RS1000220764 (19:53118123 T>C), RS1000494431 (19:53122942 ACTCCCTC>A), RS1000568842 (19:53115074 G>A), RS1000599906 (19:53114791 G>A), RS1000703636 (19:53117551 T>C), RS1000801155 (19:53111331 A>G,T), RS1001226258 (19:53120299 A>C), RS1001407479 (19:53131033 T>C), RS1001452506 (19:53114224 T>C), RS1001481541 (19:53113997 C>T), RS1001567427 (19:53134104 A>G), RS1001656363 (19:53120076 A>T), RS1001752586 (19:53107559 A>G), RS1001776468 (19:53129078 T>A,G)

Disease associations

OMIM: gene MIM:619506 | 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

23 total (human), top 23 by PubMed support.

ChemicalActions (top 5)PubMed papers
trichostatin Aaffects cotreatment, decreases expression2
Nickeldecreases expression2
Oxygendecreases expression, increases expression2
Valproic Aciddecreases expression2
GSK-J4decreases expression1
arseniteaffects binding, increases reaction1
aflatoxin B2decreases methylation1
avobenzonedecreases expression1
CGP 52608affects binding, increases reaction1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
dorsomorphinaffects cotreatment, decreases expression1
bisphenol Sdecreases expression1
Decitabinedecreases expression, decreases reaction1
Leflunomideincreases expression1
Acetaminophenincreases expression1
Air Pollutantsdecreases expression, increases abundance1
Atrazinedecreases expression1
Benzo(a)pyreneaffects methylation1
Doxorubicindecreases expression1
Smokedecreases expression, decreases reaction1
Cyclosporineincreases expression1
Aflatoxin B1affects expression1
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.