ZNF700

gene
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Also known as DKFZp434I1610

Summary

ZNF700 (zinc finger protein 700, HGNC:25292) is a protein-coding gene on chromosome 19p13.2, encoding Zinc finger protein 700 (Q9H0M5). May be involved in transcriptional regulation.

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.

Source: NCBI Gene 90592 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • MANE Select transcript: NM_144566

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25292
Approved symbolZNF700
Namezinc finger protein 700
Location19p13.2
Locus typegene with protein product
StatusApproved
AliasesDKFZp434I1610
Ensembl geneENSG00000196757
Ensembl biotypeprotein_coding
Entrez90592

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 3 protein_coding

ENST00000254321, ENST00000482090, ENST00000622593

RefSeq mRNA: 2 — MANE Select: NM_144566 NM_001271848, NM_144566

CCDS: CCDS32915, CCDS74289

Canonical transcript exons

ENST00000254321 — 4 exons

ExonStartEnd
ENSE000016708581194718111947307
ENSE000018132481194827611950763
ENSE000028202981194751411947574
ENSE000038480961192510711925273

Expression profiles

Bgee: expression breadth ubiquitous, 135 present calls, max score 87.83.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 7.6401 / max 106.2182, expressed in 1633 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1739736.68191616
1739721.6083901
1739740.9582472

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
granulocyteCL:000009487.83gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099187.74gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047387.53gold quality
metanephros cortexUBERON:001053387.22gold quality
body of pancreasUBERON:000115086.93gold quality
spleenUBERON:000210686.85gold quality
right lobe of liverUBERON:000111485.80gold quality
small intestine Peyer’s patchUBERON:000345485.59gold quality
lower esophagus mucosaUBERON:003583485.49gold quality
mucosa of transverse colonUBERON:000499185.27gold quality
transverse colonUBERON:000115785.02gold quality
endometriumUBERON:000129584.97gold quality
cortex of kidneyUBERON:000122584.68gold quality
skin of abdomenUBERON:000141684.62gold quality
zone of skinUBERON:000001484.53gold quality
calcaneal tendonUBERON:000370184.48gold quality
skin of legUBERON:000151184.47gold quality
small intestineUBERON:000210884.06gold quality
tonsilUBERON:000237283.66gold quality
body of stomachUBERON:000116183.60gold quality
pancreasUBERON:000126483.46gold quality
right ovaryUBERON:000211883.43gold quality
right adrenal gland cortexUBERON:003582783.05gold quality
right adrenal glandUBERON:000123383.02gold quality
esophagus mucosaUBERON:000246982.98gold quality
left ovaryUBERON:000211982.95gold quality
intestineUBERON:000016082.94gold quality
bone marrowUBERON:000237182.94gold quality
thoracic mammary glandUBERON:000520082.93gold quality
vaginaUBERON:000099682.81gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no3.28

Regulation

Is transcription factor: yes

JASPAR motifs

MotifNameFamily
MA2595.1ZNF700More than 3 adjacent zinc fingers

JASPAR matrix evidence (PMIDs): PMID:39605530

miRNA regulators (miRDB)

37 targeting ZNF700, 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-3064-3P100.0070.091254
HSA-MIR-188-3P100.0068.761240
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-186-5P99.9970.833707
HSA-MIR-150-5P99.9966.691976
HSA-MIR-433-3P99.9869.371203
HSA-MIR-548AA99.9670.643753
HSA-MIR-548AP-3P99.9670.643753
HSA-MIR-548T-3P99.9670.643753
HSA-MIR-3912-5P99.9566.11925
HSA-MIR-449399.9066.48977
HSA-MIR-605-3P99.8869.221833
HSA-MIR-629-3P99.8567.991875
HSA-MIR-4713-5P99.7867.801794
HSA-MIR-7154-5P99.6970.521900
HSA-MIR-875-3P99.6369.472548
HSA-MIR-612699.6268.09996
HSA-MIR-199A-5P99.5169.711107
HSA-MIR-199B-5P99.5169.741098
HSA-MIR-6507-5P99.3670.462524
HSA-MIR-296-3P99.2166.56474
HSA-MIR-376A-3P99.0669.171128
HSA-MIR-376B-3P99.0669.171128
HSA-MIR-806699.0568.661532
HSA-MIR-4742-3P98.7369.821803
HSA-MIR-548AO-5P98.5569.571362

Literature-anchored findings (GeneRIF, showing 1)

  • High ZNF700 expression is associated with colorectal cancer. (PMID:25875936)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusZfp961ENSMUSG00000052446
rattus_norvegicusZfp617ENSRNOG00000049856

Paralogs (15): ZNF14 (ENSG00000105708), ZNF57 (ENSG00000171970), ZNF791 (ENSG00000173875), ZNF443 (ENSG00000180855), ZNF101 (ENSG00000181896), ZNF563 (ENSG00000188868), ZNF799 (ENSG00000196466), ZNF441 (ENSG00000197044), ZNF433 (ENSG00000197647), ZNF44 (ENSG00000197857), ZNF823 (ENSG00000197933), ZNF442 (ENSG00000198342), ZNF844 (ENSG00000223547), ZNF709 (ENSG00000242852), ZNF878 (ENSG00000257446)

Protein

Protein identifiers

Zinc finger protein 700Q9H0M5 (reviewed: Q9H0M5)

All UniProt accessions (3): Q9H0M5, A0A087WVH9, K7EQV7

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.

RefSeq proteins (2): NP_001258777, NP_653167* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050758Znf_C2H2-typeFamily

Pfam: PF00096, PF01352

UniProt features (24 total): zinc finger region 18, sequence variant 2, chain 1, domain 1, region of interest 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9H0M5-F172.270.03

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 42 (showing top): GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_UP, GSE18804_SPLEEN_MACROPHAGE_VS_BRAIN_TUMORAL_MACROPHAGE_DN, GSE37336_LY6C_POS_VS_NEG_NAIVE_CD4_TCELL_UP, GSE18804_SPLEEN_MACROPHAGE_VS_TUMORAL_MACROPHAGE_DN, RODRIGUES_THYROID_CARCINOMA_ANAPLASTIC_UP, chr19p13, HAMAI_APOPTOSIS_VIA_TRAIL_UP, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, TOYOTA_TARGETS_OF_MIR34B_AND_MIR34C, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, FEV_TARGET_GENES, ZFP91_TARGET_GENES, ZNF350_TARGET_GENES, ZNF513_TARGET_GENES, ZNF561_TARGET_GENES

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

GO Molecular Function (5): RNA polymerase II transcription regulatory region sequence-specific DNA binding (GO:0000977), DNA-binding transcription factor activity, RNA polymerase II-specific (GO:0000981), zinc ion binding (GO:0008270), 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
transcription cis-regulatory region binding1
chromatin1
RNA polymerase II transcription regulatory region sequence-specific DNA binding1
DNA-binding transcription factor activity1
regulation of transcription by RNA polymerase II1
transition metal ion binding1
nucleic acid binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

376 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF700GPBP1L1Q9HC44571
ZNF700ZNF638Q14966474
ZNF700LINC03040Q8N319411
ZNF700ZNF346Q9UL40394
ZNF700BLTP3BA0JNW5392
ZNF700TADA2AO75478380
ZNF700NT5DC1Q5TFE4371
ZNF700NXPE4Q6UWF7371
ZNF700REP15Q6BDI9370
ZNF700FAM53AQ6NSI3368
ZNF700MAST2Q6P0Q8350
ZNF700CTDSPL2Q05D32325
ZNF700TDRPQ86YL5323
ZNF700GALNTL6Q49A17311
ZNF700SCPEP1Q9HB40302

IntAct

5 interactions, top by confidence:

ABTypeScore
ZNF700ECE1psi-mi:“MI:0915”(physical association)0.370
ECE1ZNF700psi-mi:“MI:0915”(physical association)0.370
pyrDZNF700psi-mi:“MI:0915”(physical association)0.000

BioGRID (1): ZNF700 (Affinity Capture-RNA)

ESM2 similar proteins: A6NDX5, A6NK75, A6NNF4, A6NP11, B4DXR9, B7Z6K7, C9JN71, O43361, O75290, O75373, P0CJ79, P0DKX0, P17019, P17021, P17035, P17039, P35789, Q02386, Q03938, Q08AN1, Q13106, Q15928, Q3ZCX4, Q5R9F0, Q5SXM1, Q68EA5, Q6P9A1, Q6PDB4, Q6ZN06, Q6ZN08, Q6ZNG1, Q76KX8, Q86V71, Q86XN6, Q8IYB9, Q8N4W9, Q8NEP9, Q8TBZ8, Q8TC21, Q8TF32

Diamond homologs: A2RRD8, A6NFI3, A6NM28, A8MUZ8, A8MWA4, B2RUI1, B4DU55, E9Q8G5, O43296, O43361, O75467, O75820, P0CH99, P0CI00, P10078, P16373, P16374, P17021, P17023, P17032, P17097, P17098, P21506, P51786, P52740, Q06732, Q08ER8, Q13106, Q13360, Q13398, Q14592, Q147U1, Q32M78, Q3KQV3, Q3MIS6, Q3SY52, Q571J5, Q5CZA5, Q5HY98, Q5R7I8

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

822 predictions. Top by Δscore:

VariantEffectΔscore
19:11948266:T:Gacceptor_gain1.0000
19:11948272:ACAG:Aacceptor_gain1.0000
19:11948273:CA:Cacceptor_loss1.0000
19:11948274:A:AGacceptor_gain1.0000
19:11948274:AG:Aacceptor_gain1.0000
19:11948275:G:GGacceptor_gain1.0000
19:11948275:G:GTacceptor_gain1.0000
19:11948275:GG:Gacceptor_gain1.0000
19:11948275:GGA:Gacceptor_gain1.0000
19:11948275:GGAGT:Gacceptor_gain1.0000
19:11947163:A:AGacceptor_gain0.9900
19:11947163:ACAT:Aacceptor_gain0.9900
19:11947164:C:Gacceptor_gain0.9900
19:11947165:AT:Aacceptor_gain0.9900
19:11947165:ATGT:Aacceptor_gain0.9900
19:11947166:T:Gacceptor_gain0.9900
19:11947304:ATAGG:Adonor_loss0.9900
19:11947305:TAGGT:Tdonor_loss0.9900
19:11947306:AGGT:Adonor_loss0.9900
19:11947307:GGTA:Gdonor_loss0.9900
19:11947308:G:Cdonor_loss0.9900
19:11947308:G:GGdonor_gain0.9900
19:11947309:T:Adonor_loss0.9900
19:11948265:A:AGacceptor_gain0.9900
19:11948265:AT:Aacceptor_gain0.9900
19:11948266:T:TAacceptor_gain0.9900
19:11948272:A:AGacceptor_gain0.9900
19:11948273:C:Gacceptor_gain0.9900
19:11948273:CAGG:Cacceptor_gain0.9900
19:11948274:AGGA:Aacceptor_gain0.9900

AlphaMissense

4976 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:11949825:T:CF601L0.994
19:11949827:C:AF601L0.994
19:11949827:C:GF601L0.994
19:11948799:T:CF259L0.992
19:11948801:T:AF259L0.992
19:11948801:T:GF259L0.992
19:11949909:T:CF629L0.992
19:11949911:C:AF629L0.992
19:11949911:C:GF629L0.992
19:11949741:T:CF573L0.991
19:11949743:C:AF573L0.991
19:11949743:C:GF573L0.991
19:11949657:T:CF545L0.986
19:11949659:C:AF545L0.986
19:11949659:C:GF545L0.986
19:11950077:T:CF685L0.985
19:11950079:C:AF685L0.985
19:11950079:C:GF685L0.985
19:11949915:T:CS631P0.984
19:11949928:T:CL635P0.983
19:11949993:T:CF657L0.982
19:11949995:C:AF657L0.982
19:11949995:C:GF657L0.982
19:11949387:T:CF455L0.980
19:11949389:C:AF455L0.980
19:11949389:C:GF455L0.980
19:11949747:T:CS575P0.980
19:11948967:T:CF315L0.979
19:11948969:T:AF315L0.979
19:11948969:T:GF315L0.979

dbSNP variants (sampled 300 via entrez): RS1000057418 (19:11945987 G>C), RS1000118339 (19:11941121 G>A), RS1000430019 (19:11945837 G>C), RS1000536597 (19:11923777 G>A,C), RS1000541068 (19:11941326 C>A), RS1000969615 (19:11923507 C>A), RS1001063807 (19:11929263 A>G), RS1001164018 (19:11928203 C>G,T), RS1001295190 (19:11926216 T>C,G), RS1001338425 (19:11934988 T>C,G), RS1001362078 (19:11951248 T>C), RS1001530813 (19:11942847 T>C), RS1001549126 (19:11929032 C>T), RS1001666042 (19:11951026 C>T), RS1001690762 (19:11923475 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
GCST002337_47Amyotrophic lateral sclerosis (sporadic)4.000000e-06

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

21 total (human), top 21 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Aciddecreases expression2
aristolochic acid Idecreases expression1
TAK-243increases sumoylation1
trichostatin Aaffects expression1
sodium arseniteincreases expression1
aflatoxin B2increases methylation1
Temozolomideincreases expression1
Leflunomideincreases expression1
Air Pollutantsdecreases expression, increases abundance1
Benzeneincreases expression1
Benzo(a)pyrenedecreases methylation1
Cisplatinincreases expression1
Estradiolaffects expression1
Formaldehydedecreases expression1
Hydrogen Peroxideaffects cotreatment, decreases expression1
Quercetindecreases expression1
Theophyllineaffects cotreatment, decreases expression1
Tobacco Smoke Pollutiondecreases expression1
Aflatoxin B1increases methylation1
Lactic Aciddecreases 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.