ZNF615

gene
On this page

Also known as FLJ33710

Summary

ZNF615 (zinc finger protein 615, HGNC:24740) is a protein-coding gene on chromosome 19q13.41, encoding Zinc finger protein 615 (Q8N8J6). May be involved in transcriptional regulation.

Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.

Source: NCBI Gene 284370 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 101 total
  • MANE Select transcript: NM_001199324

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:24740
Approved symbolZNF615
Namezinc finger protein 615
Location19q13.41
Locus typegene with protein product
StatusApproved
AliasesFLJ33710
Ensembl geneENSG00000197619
Ensembl biotypeprotein_coding
Entrez284370

Gene structure

Transcript identifiers

Ensembl transcripts: 19 — 15 protein_coding, 2 protein_coding_CDS_not_defined, 2 nonsense_mediated_decay

ENST00000376716, ENST00000391795, ENST00000593650, ENST00000594083, ENST00000595114, ENST00000597747, ENST00000597905, ENST00000598071, ENST00000599115, ENST00000599177, ENST00000599631, ENST00000601178, ENST00000602063, ENST00000618487, ENST00000884687, ENST00000946691, ENST00000946692, ENST00000946693, ENST00000946694

RefSeq mRNA: 9 — MANE Select: NM_001199324 NM_001199324, NM_001321317, NM_001321318, NM_001321319, NM_001321320, NM_001321321, NM_001321322, NM_001321323, NM_198480

CCDS: CCDS12846, CCDS59418, CCDS82387

Canonical transcript exons

ENST00000598071 — 7 exons

ExonStartEnd
ENSE000014032715200369752003900
ENSE000014073485200181352001908
ENSE000025263975200215552002281
ENSE000029776155200814152008211
ENSE000030474475200034652000378
ENSE000031901225199133251994837
ENSE000035531915200729352007330

Expression profiles

Bgee: expression breadth ubiquitous, 237 present calls, max score 89.95.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 5.3706 / max 129.1825, expressed in 1448 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1825115.37061448

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
cardiac muscle of right atriumUBERON:000337989.95silver quality
left ventricle myocardiumUBERON:000656689.41gold quality
kidney epitheliumUBERON:000481987.09silver quality
deltoidUBERON:000147686.80silver quality
tibialis anteriorUBERON:000138586.43silver quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099186.01gold quality
calcaneal tendonUBERON:000370184.00gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.72gold quality
corpus callosumUBERON:000233682.39gold quality
epithelial cell of pancreasCL:000008382.01silver quality
cortical plateUBERON:000534381.98gold quality
ganglionic eminenceUBERON:000402381.85gold quality
colonic epitheliumUBERON:000039781.54gold quality
prostate glandUBERON:000236781.49gold quality
superficial temporal arteryUBERON:000161480.67silver quality
ventricular zoneUBERON:000305380.52gold quality
upper arm skinUBERON:000426380.33gold quality
islet of LangerhansUBERON:000000680.07gold quality
mucosa of paranasal sinusUBERON:000503080.06silver quality
oviduct epitheliumUBERON:000480479.84gold quality
germinal epithelium of ovaryUBERON:000130479.62silver quality
ileal mucosaUBERON:000033179.53gold quality
pigmented layer of retinaUBERON:000178279.38gold quality
myocardiumUBERON:000234979.07silver quality
smooth muscle tissueUBERON:000113579.02gold quality
descending thoracic aortaUBERON:000234578.48gold quality
popliteal arteryUBERON:000225078.41gold quality
tibial arteryUBERON:000761078.40gold quality
ovaryUBERON:000099278.33gold quality
sural nerveUBERON:001548878.28gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-MTAB-6142no50.16
E-ANND-3no4.17

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): YY1

miRNA regulators (miRDB)

100 targeting ZNF615, 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-432-3P100.0067.86705
HSA-MIR-6748-5P100.0065.811057
HSA-MIR-3163100.0077.238605
HSA-MIR-4510100.0066.602050
HSA-MIR-6127100.0066.762188
HSA-MIR-6129100.0066.462080
HSA-MIR-6130100.0066.692012
HSA-MIR-6133100.0066.482064
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-7110-3P100.0073.182486
HSA-MIR-33A-5P99.9968.621055
HSA-MIR-33B-5P99.9968.581062
HSA-MIR-433-3P99.9869.371203
HSA-MIR-56899.9869.862084
HSA-MIR-4666A-3P99.9671.713434
HSA-MIR-9-3P99.9670.882068
HSA-MIR-548AJ-3P99.9673.385345
HSA-MIR-548X-3P99.9673.385345
HSA-MIR-495-3P99.9672.814197
HSA-MIR-568899.9673.234504
HSA-LET-7C-3P99.9573.422862
HSA-MIR-548J-3P99.9472.614881
HSA-MIR-548AE-3P99.9372.664867
HSA-MIR-548AH-3P99.9372.544872
HSA-MIR-548AM-3P99.9372.544872
HSA-MIR-548AQ-3P99.9372.664867
HSA-MIR-338-5P99.9272.342951

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 615Q8N8J6 (reviewed: Q8N8J6)

All UniProt accessions (7): A0A0G2JLJ6, Q8N8J6, H9KV89, M0QZR2, M0QZZ4, M0R0F8, M0R130

UniProt curated annotations — full annotation on UniProt →

Function. May be involved in transcriptional regulation.

Subcellular location. Nucleus.

Similarity. Belongs to the krueppel C2H2-type zinc-finger protein family.

Isoforms (3)

UniProt IDNamesCanonical?
Q8N8J6-11yes
Q8N8J6-22
Q8N8J6-33

RefSeq proteins (9): NP_001186253, NP_001308246, NP_001308247, NP_001308248, NP_001308249, NP_001308250, NP_001308251, NP_001308252, NP_940882 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050636C2H2-ZF_domain-containingFamily

Pfam: PF00096, PF01352

UniProt features (27 total): zinc finger region 19, sequence variant 3, splice variant 2, chain 1, domain 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8N8J6-F173.940.20

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 45 (showing top): BASAKI_YBX1_TARGETS_DN, NOUZOVA_TRETINOIN_AND_H4_ACETYLATION, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, CIITA_TARGET_GENES, E2F5_TARGET_GENES, FOXE1_TARGET_GENES, ZNF197_TARGET_GENES, ZNF711_TARGET_GENES, ZNF766_TARGET_GENES, MIR4666A_3P, MIR374A_5P, MIR374B_5P, MIR1323, MIR9_3P, MIR548O_3P

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

GO Molecular Function (4): zinc ion binding (GO:0008270), sequence-specific DNA binding (GO:0043565), DNA binding (GO:0003677), metal ion binding (GO:0046872)

GO Cellular Component (1): nucleus (GO:0005634)

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
regulation of DNA-templated transcription1
transcription by RNA polymerase II1
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
transition metal ion binding1
DNA binding1
nucleic acid binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

534 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF615CCDC158Q5M9N0419
ZNF615C5orf63A6NC05377
ZNF615SPATA12Q7Z6I5376
ZNF615CEACAM18A8MTB9375
ZNF615CCDC59Q9P031358
ZNF615SDR42E1Q8WUS8355
ZNF615ANKMY2Q8IV38348
ZNF615GIN1Q9NXP7333
ZNF615ANKRD33BA6NCL7325
ZNF615WDR36Q8NI36311
ZNF615SERPINB12Q96P63307
ZNF615GARIN6Q8NEG0293
ZNF615ANKRD49Q8WVL7289
ZNF615THSD7BQ9C0I4288
ZNF615TUBD1Q9UJT1286

IntAct

2 interactions, top by confidence:

ABTypeScore
FYNZNF615psi-mi:“MI:0915”(physical association)0.000

BioGRID (7): ZNF615 (Affinity Capture-RNA), ZNF615 (Proximity Label-MS), ZNF615 (Affinity Capture-MS), ZNF615 (Affinity Capture-MS), ZNF615 (Affinity Capture-MS), ZNF615 (Cross-Linking-MS (XL-MS)), ZNF615 (Proximity Label-MS)

ESM2 similar proteins: A2VDP4, A6NHJ4, O94892, P0CJ79, P17014, P17021, P17025, P17032, P17035, P18733, P51508, P51814, Q06730, Q06732, Q09FC8, Q0VGE8, Q14586, Q32M78, Q3MIS6, Q5JVG2, Q5R4K8, Q5R9S5, Q5RBQ3, Q5RCJ2, Q5RER9, Q5TYW1, Q5VIY5, Q6P560, Q6PDB4, Q6ZMW2, Q6ZN06, Q6ZNA1, Q76KX8, Q7L2R6, Q86Y25, Q8N184, Q8N823, Q8N883, Q8N8J6, Q8NEP9

Diamond homologs: A0JPL0, A2VDP4, A6QLU5, A6QPT6, A8MQ14, A8MUZ8, A8MWA4, B1APH4, B2RXC5, E9PYI1, E9Q8G5, O75290, O94892, P08042, P0CH99, P0CI00, P17014, P17025, P17030, P17031, P17032, P17098, P21506, P51508, P51523, P51786, P51814, P52736, P52738, Q02525, Q03923, Q03936, Q06730, Q06732, Q0VCB0, Q13401, Q14587, Q16587, Q2M218, Q2M3X9

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance91
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1118 predictions. Top by Δscore:

VariantEffectΔscore
19:51994838:C:CCacceptor_gain1.0000
19:52001810:CA:Cdonor_loss1.0000
19:52001811:A:ACdonor_gain1.0000
19:52001812:C:CCdonor_gain1.0000
19:52001812:C:Tdonor_loss1.0000
19:52001905:TACC:Tacceptor_gain1.0000
19:52001906:ACC:Aacceptor_gain1.0000
19:52001907:CC:Cacceptor_gain1.0000
19:52001907:CCC:Cacceptor_gain1.0000
19:52001907:CCCTG:Cacceptor_loss1.0000
19:52001908:CCTG:Cacceptor_gain1.0000
19:52001909:C:CCacceptor_gain1.0000
19:52001910:T:Aacceptor_loss1.0000
19:52001914:CA:Cacceptor_gain1.0000
19:52001915:A:ACacceptor_gain1.0000
19:52001915:A:Cacceptor_gain1.0000
19:52002150:CTCA:Cdonor_loss1.0000
19:52002151:TCA:Tdonor_loss1.0000
19:52002153:A:ACdonor_gain1.0000
19:52002153:A:AGdonor_loss1.0000
19:52002153:AC:Adonor_gain1.0000
19:52002154:C:CCdonor_gain1.0000
19:52002154:CC:Cdonor_gain1.0000
19:52002154:CCCA:Cdonor_gain1.0000
19:52002157:A:ACdonor_gain1.0000
19:52002158:C:CCdonor_gain1.0000
19:52002159:TGC:Tdonor_gain1.0000
19:52002161:C:CTdonor_gain1.0000
19:52002162:C:CTdonor_gain1.0000
19:52002193:T:TAdonor_gain1.0000

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000050007 (19:52006617 T>C), RS1000236821 (19:51995109 C>A,T), RS1000534207 (19:51994169 G>A), RS1001159209 (19:52001332 A>G), RS1001224813 (19:52006911 G>A), RS1001247757 (19:52009362 G>A,T), RS1001250272 (19:52002793 A>G), RS1001383853 (19:52000831 T>C), RS1001396448 (19:52001646 T>A,C,G), RS1001572860 (19:52006732 A>G), RS1001904145 (19:51995285 T>G), RS1001990285 (19:51991029 G>A,T), RS1002172539 (19:52008056 C>T), RS1002238717 (19:51998193 T>C), RS1002305230 (19:52004485 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

1 associations (top):

StudyTraitp-value
GCST007277_24Tourette syndrome9.000000e-07

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

29 total (human), top 29 by PubMed support.

ChemicalActions (top 5)PubMed papers
Tobacco Smoke Pollutionincreases expression2
Cadmium Chloridedecreases expression, increases abundance, increases expression2
3-((6-(2-methoxyphenyl)pyrimidin-4-yl)amino)phenyl)methane sulfonamidedecreases expression1
dicrotophosdecreases expression1
urushioldecreases expression1
triphenyl phosphateaffects expression1
pirinixic acidaffects binding, decreases expression, increases activity1
arseniteaffects binding, decreases reaction1
butyraldehydeincreases expression1
perfluorooctanoic aciddecreases expression1
di-n-butylphosphoric acidaffects expression1
perfluorooctane sulfonic aciddecreases expression1
CGP 52608affects binding, increases reaction1
perfluoro-n-nonanoic aciddecreases expression1
2-palmitoylglycerolincreases expression1
perfluorohexanesulfonic aciddecreases expression1
abrineincreases expression1
bisphenol Sdecreases methylation1
jinfukangdecreases expression1
Resveratrolaffects cotreatment, increases expression1
Temozolomideincreases expression1
Vehicle Emissionsincreases abundance, increases expression1
Benzeneincreases expression1
Benzo(a)pyreneaffects methylation, decreases methylation1
Cadmiumincreases abundance, increases expression1
Methyl Methanesulfonateincreases expression1
Plant Extractsaffects cotreatment, increases expression1
Urethaneincreases expression1
Particulate Matterincreases abundance, increases 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.