ZNF98
geneOn this page
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:13174 |
| Approved symbol | ZNF98 |
| Name | zinc finger protein 98 |
| Location | 19p12 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | ZNF739, F7175 |
| Ensembl gene | ENSG00000197360 |
| Ensembl biotype | protein_coding |
| OMIM | 603980 |
| Entrez | 148198 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00001433568 | 22391019 | 22392981 |
| ENSE00001549541 | 22422195 | 22422346 |
| ENSE00002283366 | 22402789 | 22402884 |
| ENSE00003650572 | 22403386 | 22403512 |
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 ID | TPM avg | Samples expressed |
|---|---|---|
| 180253 | 0.6358 | 118 |
| 180252 | 0.3191 | 121 |
| 180251 | 0.2054 | 73 |
Top tissues by expression
136 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 89.69 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 85.67 | gold quality |
| body of pancreas | UBERON:0001150 | 81.31 | gold quality |
| pancreas | UBERON:0001264 | 77.87 | gold quality |
| caudate nucleus | UBERON:0001873 | 77.57 | gold quality |
| quadriceps femoris | UBERON:0001377 | 75.83 | gold quality |
| putamen | UBERON:0001874 | 75.32 | gold quality |
| cerebellar vermis | UBERON:0004720 | 74.40 | gold quality |
| testis | UBERON:0000473 | 73.74 | gold quality |
| left ovary | UBERON:0002119 | 72.07 | gold quality |
| left testis | UBERON:0004533 | 72.07 | gold quality |
| right testis | UBERON:0004534 | 72.03 | gold quality |
| ovary | UBERON:0000992 | 71.75 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 71.53 | gold quality |
| islet of Langerhans | UBERON:0000006 | 71.50 | gold quality |
| primary visual cortex | UBERON:0002436 | 71.36 | gold quality |
| right frontal lobe | UBERON:0002810 | 70.67 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 69.79 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 69.32 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 68.92 | gold quality |
| right ovary | UBERON:0002118 | 68.44 | gold quality |
| cerebral cortex | UBERON:0000956 | 68.38 | gold quality |
| ventricular zone | UBERON:0003053 | 67.99 | gold quality |
| frontal cortex | UBERON:0001870 | 67.97 | gold quality |
| adrenal tissue | UBERON:0018303 | 66.51 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 66.33 | gold quality |
| prefrontal cortex | UBERON:0000451 | 65.75 | gold quality |
| nucleus accumbens | UBERON:0001882 | 65.19 | gold quality |
| ganglionic eminence | UBERON:0004023 | 63.98 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 63.94 | gold quality |
Single-cell (SCXA)
Detected in 3 experiment(s), a significant marker in 2.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-MTAB-6819 | yes | 132.09 |
| E-ANND-3 | yes | 7.23 |
| E-HCAD-30 | no | 491.37 |
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):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-3064-3P | 100.00 | 70.09 | 1254 |
| HSA-MIR-4776-3P | 100.00 | 68.73 | 1340 |
| HSA-MIR-548AN | 99.97 | 70.91 | 2817 |
| HSA-MIR-493-5P | 99.96 | 72.47 | 2382 |
| HSA-MIR-1297 | 99.91 | 73.41 | 3162 |
| HSA-MIR-3529-3P | 99.90 | 73.55 | 3045 |
| HSA-MIR-383-3P | 99.85 | 65.84 | 1359 |
| HSA-MIR-4645-3P | 99.76 | 69.33 | 993 |
| HSA-MIR-7156-5P | 99.64 | 68.81 | 1369 |
| HSA-MIR-7152-5P | 99.60 | 69.33 | 2094 |
| HSA-MIR-6740-3P | 99.48 | 68.49 | 1392 |
| HSA-MIR-4728-3P | 99.47 | 68.94 | 981 |
| HSA-MIR-4273 | 99.45 | 67.93 | 1206 |
| HSA-MIR-19A-5P | 99.36 | 66.93 | 1675 |
| HSA-MIR-19B-1-5P | 99.36 | 67.07 | 1669 |
| HSA-MIR-19B-2-5P | 99.36 | 67.07 | 1669 |
| HSA-MIR-155-5P | 99.35 | 70.16 | 1509 |
| HSA-MIR-12113 | 99.32 | 67.54 | 1072 |
| HSA-MIR-6768-3P | 99.14 | 67.38 | 1319 |
| HSA-MIR-140-3P | 99.04 | 67.69 | 1324 |
| HSA-MIR-4539 | 98.78 | 67.18 | 888 |
| HSA-MIR-34B-3P | 98.70 | 67.40 | 1171 |
| HSA-MIR-216B-3P | 98.55 | 67.19 | 1223 |
| HSA-MIR-1914-5P | 97.83 | 66.21 | 807 |
| HSA-MIR-8055 | 97.62 | 66.09 | 1023 |
| HSA-MIR-500A-3P | 97.60 | 67.48 | 595 |
| HSA-MIR-6500-3P | 97.42 | 67.20 | 867 |
| HSA-MIR-3152-5P | 96.98 | 66.88 | 819 |
| HSA-MIR-4680-5P | 96.43 | 67.15 | 893 |
| HSA-MIR-4484 | 96.35 | 64.08 | 382 |
Cross-species orthologs
1 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | ENSDARG00000099025 |
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 98 — A6NK75 (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)
| ID | Name | Type |
|---|---|---|
| IPR001909 | KRAB | Domain |
| IPR013087 | Znf_C2H2_type | Domain |
| IPR036051 | KRAB_dom_sf | Homologous_superfamily |
| IPR036236 | Znf_C2H2_sf | Homologous_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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A6NK75-F1 | 72.72 | 0.24 |
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:
| Category | Terms |
|---|---|
| RNA polymerase II transcription regulatory region sequence-specific DNA binding | 3 |
| regulation of transcription by RNA polymerase II | 2 |
| transcription by RNA polymerase II | 2 |
| DNA-templated transcription | 1 |
| regulation of gene expression | 1 |
| regulation of RNA biosynthetic process | 1 |
| negative regulation of DNA-templated transcription | 1 |
| regulation of DNA-templated transcription | 1 |
| cis-regulatory region sequence-specific DNA binding | 1 |
| chromatin | 1 |
| DNA-binding transcription factor activity | 1 |
| negative regulation of transcription by RNA polymerase II | 1 |
| DNA-binding transcription factor activity, RNA polymerase II-specific | 1 |
| DNA-binding transcription repressor activity | 1 |
| transition metal ion binding | 1 |
| nucleic acid binding | 1 |
| cation binding | 1 |
| intracellular membrane-bounded organelle | 1 |
Protein interactions and networks
STRING
334 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| ZNF98 | DTWD1 | Q8N5C7 | 567 |
| ZNF98 | TMEM14B | Q9NUH8 | 471 |
| ZNF98 | SACK1F | Q8NEG4 | 447 |
| ZNF98 | ANKRD20A4P | Q4UJ75 | 447 |
| ZNF98 | ANKRD20A2P | Q5SQ80 | 447 |
| ZNF98 | RNF166 | Q96A37 | 398 |
| ZNF98 | GLIPR1L2 | Q4G1C9 | 392 |
| ZNF98 | FAM72B | Q86X60 | 387 |
| ZNF98 | VCF2 | Q5XKR9 | 377 |
| ZNF98 | FAM72C | H0Y354 | 373 |
| ZNF98 | KRTAP9-2 | Q9BYQ4 | 370 |
| ZNF98 | FAM72A | Q5TYM5 | 367 |
| ZNF98 | DHRS13 | Q6UX07 | 366 |
| ZNF98 | FRG2C | A6NGY1 | 359 |
| ZNF98 | ZNG1F | Q4V339 | 358 |
| ZNF98 | ZNG1C | Q5JTY5 | 358 |
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):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 89 |
| Likely benign | 10 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
656 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 19:22403425:T:A | donor_gain | 1.0000 |
| 19:22392979:CAA:C | acceptor_gain | 0.9900 |
| 19:22392982:C:CC | acceptor_gain | 0.9900 |
| 19:22402882:TAC:T | acceptor_gain | 0.9900 |
| 19:22402883:ACCTG:A | acceptor_loss | 0.9900 |
| 19:22402884:CCTGT:C | acceptor_loss | 0.9900 |
| 19:22402887:G:C | acceptor_loss | 0.9900 |
| 19:22403378:ATCCT:A | donor_loss | 0.9900 |
| 19:22403380:CCTCA:C | donor_loss | 0.9900 |
| 19:22403381:CTCA:C | donor_loss | 0.9900 |
| 19:22403382:TCAC:T | donor_loss | 0.9900 |
| 19:22403383:C:CA | donor_loss | 0.9900 |
| 19:22403384:A:AC | donor_gain | 0.9900 |
| 19:22403384:A:AT | donor_loss | 0.9900 |
| 19:22403384:AC:A | donor_gain | 0.9900 |
| 19:22403385:C:CA | donor_loss | 0.9900 |
| 19:22403385:C:CC | donor_gain | 0.9900 |
| 19:22403385:CC:C | donor_gain | 0.9900 |
| 19:22403385:CCCA:C | donor_gain | 0.9900 |
| 19:22403509:CTCC:C | acceptor_gain | 0.9900 |
| 19:22403511:CC:C | acceptor_gain | 0.9900 |
| 19:22403512:CC:C | acceptor_gain | 0.9900 |
| 19:22403512:CCTG:C | acceptor_loss | 0.9900 |
| 19:22403513:CTGAA:C | acceptor_loss | 0.9900 |
| 19:22403514:T:A | acceptor_loss | 0.9900 |
| 19:22405206:A:AC | donor_gain | 0.9900 |
| 19:22405207:C:CC | donor_gain | 0.9900 |
| 19:22392977:TACAA:T | acceptor_gain | 0.9800 |
| 19:22402784:CCTA:C | donor_loss | 0.9800 |
| 19:22402786:TACC:T | donor_loss | 0.9800 |
AlphaMissense
3803 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 19:22391822:A:C | F471L | 0.993 |
| 19:22391822:A:T | F471L | 0.993 |
| 19:22391824:A:G | F471L | 0.993 |
| 19:22391906:A:C | F443L | 0.993 |
| 19:22391906:A:T | F443L | 0.993 |
| 19:22391908:A:G | F443L | 0.993 |
| 19:22391738:A:C | F499L | 0.991 |
| 19:22391738:A:T | F499L | 0.991 |
| 19:22391740:A:G | F499L | 0.991 |
| 19:22391654:A:C | F527L | 0.984 |
| 19:22391654:A:T | F527L | 0.984 |
| 19:22391656:A:G | F527L | 0.984 |
| 19:22391889:A:G | L449P | 0.983 |
| 19:22392494:A:C | F247L | 0.981 |
| 19:22392494:A:T | F247L | 0.981 |
| 19:22392496:A:G | F247L | 0.981 |
| 19:22391721:A:G | L505P | 0.980 |
| 19:22392326:A:C | F303L | 0.976 |
| 19:22392326:A:T | F303L | 0.976 |
| 19:22392328:A:G | F303L | 0.976 |
| 19:22392242:A:C | F331L | 0.974 |
| 19:22392242:A:T | F331L | 0.974 |
| 19:22392244:A:G | F331L | 0.974 |
| 19:22392410:A:C | F275L | 0.973 |
| 19:22392410:A:T | F275L | 0.973 |
| 19:22392412:A:G | F275L | 0.973 |
| 19:22391990:A:C | F415L | 0.969 |
| 19:22391990:A:T | F415L | 0.969 |
| 19:22391992:A:G | F415L | 0.969 |
| 19:22392158:A:C | F359L | 0.969 |
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):
| Study | Trait | p-value |
|---|---|---|
| GCST001408_8 | Response to statins (LDL cholesterol change) | 3.000000e-07 |
| GCST001713_26 | Dental caries | 1.000000e-06 |
| GCST001786_25 | Dental caries | 3.000000e-06 |
| GCST004138_7 | Early-onset Parkinson’s disease | 6.000000e-25 |
| GCST006186_7 | Systolic blood pressure x smoking status (current vs non-current) interaction (1df test) | 2.000000e-07 |
| GCST006195_93 | Systolic blood pressure x smoking status (current vs non-current) interaction (2df test) | 4.000000e-08 |
| GCST90093092_5 | DHEAS levels | 2.000000e-06 |
EFO canonical traits (4, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0007804 | LDL cholesterol change measurement |
| EFO:0006335 | systolic blood pressure |
| EFO:0006527 | smoking status measurement |
| EFO:0007001 | dehydroepiandrosterone 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.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): dental caries