ZNF98

gene
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Also known as ZNF739F7175

Summary

ZNF98 (zinc finger protein 98, HGNC:13174) is a protein-coding gene on chromosome 19p12, encoding Zinc finger protein 98 (A6NK75). May be 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 DNA-templated transcription. Predicted to be located in nucleus.

Source: NCBI Gene 148198 — RefSeq curated summary.

At a glance

  • GWAS associations: 7
  • Clinical variants (ClinVar): 103 total
  • MANE Select transcript: NM_001098626

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:13174
Approved symbolZNF98
Namezinc finger protein 98
Location19p12
Locus typegene with protein product
StatusApproved
AliasesZNF739, F7175
Ensembl geneENSG00000197360
Ensembl biotypeprotein_coding
OMIM603980
Entrez148198

Gene structure

Transcript identifiers

Ensembl transcripts: 5 — 4 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000357774, ENST00000593657, ENST00000593802, ENST00000599879, ENST00000601553

RefSeq mRNA: 1 — MANE Select: NM_001098626 NM_001098626

CCDS: CCDS46031

Canonical transcript exons

ENST00000357774 — 4 exons

ExonStartEnd
ENSE000014335682239101922392981
ENSE000015495412242219522422346
ENSE000022833662240278922402884
ENSE000036505722240338622403512

Expression profiles

Bgee: expression breadth ubiquitous, 128 present calls, max score 89.69.

FANTOM5 (CAGE): breadth broad, TPM avg 1.1603 / max 114.8289, expressed in 204 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1802530.6358118
1802520.3191121
1802510.205473

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047389.69gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099185.67gold quality
body of pancreasUBERON:000115081.31gold quality
pancreasUBERON:000126477.87gold quality
caudate nucleusUBERON:000187377.57gold quality
quadriceps femorisUBERON:000137775.83gold quality
putamenUBERON:000187475.32gold quality
cerebellar vermisUBERON:000472074.40gold quality
testisUBERON:000047373.74gold quality
left ovaryUBERON:000211972.07gold quality
left testisUBERON:000453372.07gold quality
right testisUBERON:000453472.03gold quality
ovaryUBERON:000099271.75gold quality
dorsolateral prefrontal cortexUBERON:000983471.53gold quality
islet of LangerhansUBERON:000000671.50gold quality
primary visual cortexUBERON:000243671.36gold quality
right frontal lobeUBERON:000281070.67gold quality
anterior cingulate cortexUBERON:000983569.79gold quality
superior frontal gyrusUBERON:000266169.32gold quality
Brodmann (1909) area 9UBERON:001354068.92gold quality
right ovaryUBERON:000211868.44gold quality
cerebral cortexUBERON:000095668.38gold quality
ventricular zoneUBERON:000305367.99gold quality
frontal cortexUBERON:000187067.97gold quality
adrenal tissueUBERON:001830366.51gold quality
smooth muscle tissueUBERON:000113566.33gold quality
prefrontal cortexUBERON:000045165.75gold quality
nucleus accumbensUBERON:000188265.19gold quality
ganglionic eminenceUBERON:000402363.98gold quality
descending thoracic aortaUBERON:000234563.94gold quality

Single-cell (SCXA)

Detected in 3 experiment(s), a significant marker in 2.

ExperimentMarker?Max mean expression
E-MTAB-6819yes132.09
E-ANND-3yes7.23
E-HCAD-30no491.37

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

30 targeting ZNF98, 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-3064-3P100.0070.091254
HSA-MIR-4776-3P100.0068.731340
HSA-MIR-548AN99.9770.912817
HSA-MIR-493-5P99.9672.472382
HSA-MIR-129799.9173.413162
HSA-MIR-3529-3P99.9073.553045
HSA-MIR-383-3P99.8565.841359
HSA-MIR-4645-3P99.7669.33993
HSA-MIR-7156-5P99.6468.811369
HSA-MIR-7152-5P99.6069.332094
HSA-MIR-6740-3P99.4868.491392
HSA-MIR-4728-3P99.4768.94981
HSA-MIR-427399.4567.931206
HSA-MIR-19A-5P99.3666.931675
HSA-MIR-19B-1-5P99.3667.071669
HSA-MIR-19B-2-5P99.3667.071669
HSA-MIR-155-5P99.3570.161509
HSA-MIR-1211399.3267.541072
HSA-MIR-6768-3P99.1467.381319
HSA-MIR-140-3P99.0467.691324
HSA-MIR-453998.7867.18888
HSA-MIR-34B-3P98.7067.401171
HSA-MIR-216B-3P98.5567.191223
HSA-MIR-1914-5P97.8366.21807
HSA-MIR-805597.6266.091023
HSA-MIR-500A-3P97.6067.48595
HSA-MIR-6500-3P97.4267.20867
HSA-MIR-3152-5P96.9866.88819
HSA-MIR-4680-5P96.4367.15893
HSA-MIR-448496.3564.08382

Cross-species orthologs

1 orthologs

OrganismSymbolGene ID
danio_rerioENSDARG00000099025

Paralogs (18): ZNF430 (ENSG00000118620), ZNF92 (ENSG00000146757), ZNF66 (ENSG00000160229), ZNF22 (ENSG00000165512), ZNF680 (ENSG00000173041), ZNF114 (ENSG00000178150), ZFP41 (ENSG00000181638), ZNF730 (ENSG00000183850), ZNF479 (ENSG00000185177), ZNF626 (ENSG00000188171), ZNF431 (ENSG00000196705), ZNF100 (ENSG00000197020), ZNF257 (ENSG00000197134), ZNF675 (ENSG00000197372), ZNF273 (ENSG00000198039), ZNF737 (ENSG00000237440), ZNF253 (ENSG00000256771), ZNF723 (ENSG00000268696)

Protein

Protein identifiers

Zinc finger protein 98A6NK75 (reviewed: A6NK75)

Alternative names: Zinc finger protein 739, Zinc finger protein F7175

All UniProt accessions (4): A6NK75, M0QZH9, M0QZS3, M0R243

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 (1): NP_001092096* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (16 total): zinc finger region 13, chain 1, domain 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A6NK75-F172.720.24

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 18 (showing top): chr19p12, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOBP_NEGATIVE_REGULATION_OF_TRANSCRIPTION_BY_RNA_POLYMERASE_II, GOBP_NEGATIVE_REGULATION_OF_NUCLEOBASE_CONTAINING_COMPOUND_METABOLIC_PROCESS, GOMF_DNA_BINDING_TRANSCRIPTION_REPRESSOR_ACTIVITY, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, MIR155_5P, MIR7156_5P, MIR216B_3P, MIR4273, MIR383_3P, MIR500A_3P, MIR1914_5P, DESCARTES_MAIN_FETAL_ADRENOCORTICAL_CELLS, GOMF_DNA_BINDING_TRANSCRIPTION_FACTOR_ACTIVITY

GO Biological Process (3): regulation of DNA-templated transcription (GO:0006355), negative regulation of transcription by RNA polymerase II (GO:0000122), regulation of transcription by RNA polymerase II (GO:0006357)

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), DNA-binding transcription repressor activity, RNA polymerase II-specific (GO:0001227), zinc ion binding (GO:0008270), DNA binding (GO:0003677), metal ion binding (GO:0046872)

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

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
RNA polymerase II transcription regulatory region sequence-specific DNA binding3
regulation of transcription by RNA polymerase II2
transcription by RNA polymerase II2
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
negative regulation of DNA-templated transcription1
regulation of DNA-templated transcription1
cis-regulatory region sequence-specific DNA binding1
chromatin1
DNA-binding transcription factor activity1
negative regulation of transcription by RNA polymerase II1
DNA-binding transcription factor activity, RNA polymerase II-specific1
DNA-binding transcription repressor activity1
transition metal ion binding1
nucleic acid binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

334 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF98DTWD1Q8N5C7567
ZNF98TMEM14BQ9NUH8471
ZNF98SACK1FQ8NEG4447
ZNF98ANKRD20A4PQ4UJ75447
ZNF98ANKRD20A2PQ5SQ80447
ZNF98RNF166Q96A37398
ZNF98GLIPR1L2Q4G1C9392
ZNF98FAM72BQ86X60387
ZNF98VCF2Q5XKR9377
ZNF98FAM72CH0Y354373
ZNF98KRTAP9-2Q9BYQ4370
ZNF98FAM72AQ5TYM5367
ZNF98DHRS13Q6UX07366
ZNF98FRG2CA6NGY1359
ZNF98ZNG1FQ4V339358
ZNF98ZNG1CQ5JTY5358

IntAct

0 interactions, top by confidence:

BioGRID (1): ZNF98 (Affinity Capture-MS)

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: A0A1W2PQL4, A6NK75, A6NN14, A6NNF4, A6NP11, A8MQ14, A8MTY0, A8MUV8, A8MXY4, B4DX44, B4DXR9, E9PYI1, O14628, O43345, O75290, O75346, O75373, O75437, O95780, P0CB33, P0DKX0, P0DPD5, P16373, P17019, P17038, P21506, P35789, P52736, P52738, P52744, Q03923, Q03924, Q03936, Q03938, Q05481, Q14586, Q14593, Q14929, Q15928, Q3KNS6

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 significance89
Likely benign10
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

656 predictions. Top by Δscore:

VariantEffectΔscore
19:22403425:T:Adonor_gain1.0000
19:22392979:CAA:Cacceptor_gain0.9900
19:22392982:C:CCacceptor_gain0.9900
19:22402882:TAC:Tacceptor_gain0.9900
19:22402883:ACCTG:Aacceptor_loss0.9900
19:22402884:CCTGT:Cacceptor_loss0.9900
19:22402887:G:Cacceptor_loss0.9900
19:22403378:ATCCT:Adonor_loss0.9900
19:22403380:CCTCA:Cdonor_loss0.9900
19:22403381:CTCA:Cdonor_loss0.9900
19:22403382:TCAC:Tdonor_loss0.9900
19:22403383:C:CAdonor_loss0.9900
19:22403384:A:ACdonor_gain0.9900
19:22403384:A:ATdonor_loss0.9900
19:22403384:AC:Adonor_gain0.9900
19:22403385:C:CAdonor_loss0.9900
19:22403385:C:CCdonor_gain0.9900
19:22403385:CC:Cdonor_gain0.9900
19:22403385:CCCA:Cdonor_gain0.9900
19:22403509:CTCC:Cacceptor_gain0.9900
19:22403511:CC:Cacceptor_gain0.9900
19:22403512:CC:Cacceptor_gain0.9900
19:22403512:CCTG:Cacceptor_loss0.9900
19:22403513:CTGAA:Cacceptor_loss0.9900
19:22403514:T:Aacceptor_loss0.9900
19:22405206:A:ACdonor_gain0.9900
19:22405207:C:CCdonor_gain0.9900
19:22392977:TACAA:Tacceptor_gain0.9800
19:22402784:CCTA:Cdonor_loss0.9800
19:22402786:TACC:Tdonor_loss0.9800

AlphaMissense

3803 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:22391822:A:CF471L0.993
19:22391822:A:TF471L0.993
19:22391824:A:GF471L0.993
19:22391906:A:CF443L0.993
19:22391906:A:TF443L0.993
19:22391908:A:GF443L0.993
19:22391738:A:CF499L0.991
19:22391738:A:TF499L0.991
19:22391740:A:GF499L0.991
19:22391654:A:CF527L0.984
19:22391654:A:TF527L0.984
19:22391656:A:GF527L0.984
19:22391889:A:GL449P0.983
19:22392494:A:CF247L0.981
19:22392494:A:TF247L0.981
19:22392496:A:GF247L0.981
19:22391721:A:GL505P0.980
19:22392326:A:CF303L0.976
19:22392326:A:TF303L0.976
19:22392328:A:GF303L0.976
19:22392242:A:CF331L0.974
19:22392242:A:TF331L0.974
19:22392244:A:GF331L0.974
19:22392410:A:CF275L0.973
19:22392410:A:TF275L0.973
19:22392412:A:GF275L0.973
19:22391990:A:CF415L0.969
19:22391990:A:TF415L0.969
19:22391992:A:GF415L0.969
19:22392158:A:CF359L0.969

dbSNP variants (sampled 300 via entrez): RS1000141332 (19:22390777 C>A), RS1000201478 (19:22390579 TA>T,TAA), RS1000285273 (19:22403042 T>C), RS1000311900 (19:22396648 T>C), RS1000443447 (19:22402649 T>C), RS1000619349 (19:22401656 T>C), RS1000968036 (19:22407432 G>A), RS1001108250 (19:22422600 G>A), RS1001393658 (19:22412201 A>T), RS1001422475 (19:22418108 A>G), RS1001544140 (19:22421372 T>C), RS1001696669 (19:22423483 G>A), RS1001910524 (19:22416495 T>C), RS1002057019 (19:22421639 T>C), RS1002279672 (19:22422680 T>C)

Disease associations

OMIM: gene MIM:603980 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

7 associations (top):

StudyTraitp-value
GCST001408_8Response to statins (LDL cholesterol change)3.000000e-07
GCST001713_26Dental caries1.000000e-06
GCST001786_25Dental caries3.000000e-06
GCST004138_7Early-onset Parkinson’s disease6.000000e-25
GCST006186_7Systolic blood pressure x smoking status (current vs non-current) interaction (1df test)2.000000e-07
GCST006195_93Systolic blood pressure x smoking status (current vs non-current) interaction (2df test)4.000000e-08
GCST90093092_5DHEAS levels2.000000e-06

EFO canonical traits (4, from GWAS)

EFO IDTrait name
EFO:0007804LDL cholesterol change measurement
EFO:0006335systolic blood pressure
EFO:0006527smoking status measurement
EFO:0007001dehydroepiandrosterone sulphate measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): dental caries