ZNF625

gene
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Summary

ZNF625 (zinc finger protein 625, HGNC:30571) is a protein-coding gene on chromosome 19p13.2, encoding Zinc finger protein 625 (Q96I27). 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 90589 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 36 total
  • MANE Select transcript: NM_145233

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:30571
Approved symbolZNF625
Namezinc finger protein 625
Location19p13.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000257591
Ensembl biotypeprotein_coding
Entrez90589

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 3 protein_coding

ENST00000414892, ENST00000439556, ENST00000455799

RefSeq mRNA: 1 — MANE Select: NM_145233 NM_145233

CCDS: CCDS12269

Canonical transcript exons

ENST00000439556 — 4 exons

ExonStartEnd
ENSE000016280581214489012146224
ENSE000023532311215655612156734
ENSE000034673031214767612147802
ENSE000036224381214739512147455

Expression profiles

Bgee: expression breadth ubiquitous, 160 present calls, max score 86.07.

FANTOM5 (CAGE): breadth broad, TPM avg 0.6641 / max 22.7727, expressed in 358 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1792915.48301413
1792900.4125214
1792920.2516115

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
ventricular zoneUBERON:000305386.07gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099185.80gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.00gold quality
ganglionic eminenceUBERON:000402381.63gold quality
cortical plateUBERON:000534377.23gold quality
calcaneal tendonUBERON:000370175.06gold quality
adrenal tissueUBERON:001830373.55gold quality
stromal cell of endometriumCL:000225572.83gold quality
metanephros cortexUBERON:001053370.22gold quality
granulocyteCL:000009469.78gold quality
right hemisphere of cerebellumUBERON:001489069.70gold quality
islet of LangerhansUBERON:000000669.68gold quality
cerebellar cortexUBERON:000212969.56gold quality
cerebellar hemisphereUBERON:000224569.49gold quality
right lobe of thyroid glandUBERON:000111969.42gold quality
sural nerveUBERON:001548869.38gold quality
right adrenal gland cortexUBERON:003582768.87gold quality
left adrenal glandUBERON:000123468.71gold quality
left adrenal gland cortexUBERON:003582568.58gold quality
adenohypophysisUBERON:000219668.51gold quality
left lobe of thyroid glandUBERON:000112068.38gold quality
right adrenal glandUBERON:000123368.18gold quality
smooth muscle tissueUBERON:000113568.14gold quality
olfactory segment of nasal mucosaUBERON:000538668.11gold quality
tendonUBERON:000004368.08gold quality
hypothalamusUBERON:000189868.02gold quality
cerebellumUBERON:000203767.95gold quality
thyroid glandUBERON:000204667.78gold quality
adrenal glandUBERON:000236967.62gold quality
descending thoracic aortaUBERON:000234567.51gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.64

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

13 targeting ZNF625, 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-150-5P99.9966.691976
HSA-MIR-2681-5P99.7567.641655
HSA-MIR-6815-3P99.1368.981530
HSA-MIR-939-3P98.9765.072347
HSA-MIR-6895-3P98.7965.69996
HSA-MIR-60698.7267.34960
HSA-MIR-619-5P98.5764.971988
HSA-MIR-4799-3P97.7865.97893
HSA-MIR-4720-5P97.4665.67893
HSA-MIR-5588-5P97.4665.70913
HSA-MIR-134-5P97.1166.52976
HSA-MIR-311897.1166.58984
HSA-MIR-450A-5P93.8964.5750

Cross-species orthologs

0 orthologs

Paralogs (51): WIZ (ENSG00000011451), ZNF416 (ENSG00000083817), MYNN (ENSG00000085274), PRDM4 (ENSG00000110851), PRDM2 (ENSG00000116731), ZBTB17 (ENSG00000116809), ZNF644 (ENSG00000122482), GZF1 (ENSG00000125812), ZNF426 (ENSG00000130818), ZNF287 (ENSG00000141040), ZNF697 (ENSG00000143067), ZNF687 (ENSG00000143373), ZNF214 (ENSG00000149050), ZNF547 (ENSG00000152433), ZNF776 (ENSG00000152443), ZNF230 (ENSG00000159882), ZNF222 (ENSG00000159885), ZNF233 (ENSG00000159915), ZNF333 (ENSG00000160961), ZNF319 (ENSG00000166188), ZNF592 (ENSG00000166716), ZNF646 (ENSG00000167395), ZNF507 (ENSG00000168813), ZNF768 (ENSG00000169957), ZNF417 (ENSG00000173480), ZNF408 (ENSG00000175213), ZBTB41 (ENSG00000177888), ZNF223 (ENSG00000178386), ZNF852 (ENSG00000178917), ZNF784 (ENSG00000179922), ZNF572 (ENSG00000180938), ZNF707 (ENSG00000181135), ZNF746 (ENSG00000181220), ZNF467 (ENSG00000181444), ZNF530 (ENSG00000183647), ZNF17 (ENSG00000186272), ZNF527 (ENSG00000189164), ZKSCAN7 (ENSG00000196345), ZNF34 (ENSG00000196378), ZNF774 (ENSG00000196391)

Protein

Protein identifiers

Zinc finger protein 625Q96I27 (reviewed: Q96I27)

All UniProt accessions (3): Q96I27, F2Z3I2, H7C2C9

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 (2)

UniProt IDNamesCanonical?
Q96I27-11yes
Q96I27-22

RefSeq proteins (1): NP_660276* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR013087Znf_C2H2_typeDomain
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF13912

UniProt features (14 total): zinc finger region 9, chain 1, region of interest 1, modified residue 1, splice variant 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96I27-F176.260.52

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (1): 209

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 18 (showing top): GOZGIT_ESR1_TARGETS_DN, chr19p13, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ZNF350_TARGET_GENES, ZNF513_TARGET_GENES, GSE11864_CSF1_IFNG_VS_CSF1_PAM3CYS_IN_MAC_DN, MIR6895_3P, SMN1_SMN2_TARGET_GENES, SCHERER_PBMC_APSV_WETVAX_AGE_18_32YO_50_TO_60DY_UP, GSE17974_0H_VS_0.5H_IN_VITRO_ACT_CD4_TCELL_UP, GSE17974_0H_VS_1H_IN_VITRO_ACT_CD4_TCELL_UP, GOMF_DNA_BINDING_TRANSCRIPTION_FACTOR_ACTIVITY, GSE26928_NAIVE_VS_CXCR5_POS_CD4_TCELL_DN, GSE29614_CTRL_VS_TIV_FLU_VACCINE_PBMC_2007_DN

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 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), protein binding (GO:0005515), 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
binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

306 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF625A0A087WYV9A0A087WYV9507
ZNF625A0A0A6YYL1A0A0A6YYL1447
ZNF625BEND5Q7L4P6397
ZNF625MDFIQ99750348
ZNF625CCDC180Q9P1Z9348
ZNF625DMRTC2Q8IXT2347
ZNF625ZGLP1P0C6A0334
ZNF625AMER2Q8N7J2323
ZNF625TMEM240Q5SV17322
ZNF625LRRC31Q6UY01317
ZNF625TAF6LQ9Y6J9306
ZNF625GNA15P30679303
ZNF625RUNDC3BQ96NL0293
ZNF625MIER3Q7Z3K6278
ZNF625ZNF385BQ569K4274

IntAct

19 interactions, top by confidence:

ABTypeScore
ZNF625KRTAP10-4psi-mi:“MI:0915”(physical association)0.560
KRTAP10-7ZNF625psi-mi:“MI:0915”(physical association)0.560
KRTAP10-9ZNF625psi-mi:“MI:0915”(physical association)0.560
ZNF625KRT40psi-mi:“MI:0915”(physical association)0.560
ZNF625psi-mi:“MI:0915”(physical association)0.560
KRTAP10-4ZNF625psi-mi:“MI:0915”(physical association)0.560
ZNF625psi-mi:“MI:0915”(physical association)0.560
ZNF625KRTAP10-9psi-mi:“MI:0915”(physical association)0.560
ECE1ZNF625psi-mi:“MI:0915”(physical association)0.370
CBX5ZNF568psi-mi:“MI:0914”(association)0.350
ZNF625GGPS1psi-mi:“MI:0914”(association)0.350

BioGRID (14): KRT40 (Two-hybrid), KRTAP10-4 (Two-hybrid), KRTAP10-7 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-3 (Two-hybrid), ZNF625 (Reconstituted Complex), ZNF625 (Two-hybrid), ZNF625 (Two-hybrid), ZNF625 (Proximity Label-MS), RRBP1 (Proximity Label-MS), KPRP (Affinity Capture-MS), GGPS1 (Affinity Capture-MS), ZNF625 (Affinity Capture-MS), ZNF625 (Affinity Capture-MS)

ESM2 similar proteins: A0A1W2PQL4, A6NK53, A8MUZ8, A8MWA4, B1APH4, E7ETH6, O14628, O60384, P0CH99, P0CI00, P17024, P21506, P51502, P52741, P52743, P52744, Q0D2J5, Q13360, Q14593, Q15940, Q15973, Q4R882, Q5FWF6, Q5HY98, Q5JVG8, Q5RES8, Q6NX49, Q6P280, Q6V9R5, Q6ZN79, Q7L945, Q8BZW4, Q8IVC4, Q8IW36, Q8IZC7, Q8N587, Q8NDP4, Q8NE65, Q96H40, Q96I27

Diamond homologs: A0JPK3, A2RRD8, A2VDQ7, A3KN32, A8MUZ8, A8MWA4, C9JN71, E9QAG8, O60384, O60765, O75820, P0CH99, P0CI00, P10076, P10755, P15621, P16374, P16415, P17017, P17024, P51523, P52737, P52740, Q06730, Q06732, Q08AG5, Q0D2J5, Q13106, Q13360, Q15928, Q15935, Q15973, Q32M78, Q3KP31, Q4R4C7, Q4R6J4, Q4R882, Q5R9F0, Q5RC79, Q5REI6

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance36
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

862 predictions. Top by Δscore:

VariantEffectΔscore
19:12146223:CT:Cacceptor_gain1.0000
19:12146225:C:CCacceptor_gain1.0000
19:12147671:CTTA:Cdonor_loss1.0000
19:12147672:TTA:Tdonor_loss1.0000
19:12147673:TACCT:Tdonor_loss1.0000
19:12147674:A:ACdonor_gain1.0000
19:12147675:C:CCdonor_gain1.0000
19:12147675:C:CTdonor_loss1.0000
19:12147675:CCTA:Cdonor_gain1.0000
19:12147801:TC:Tacceptor_gain1.0000
19:12147802:CC:Cacceptor_gain1.0000
19:12147813:CCACA:Cacceptor_gain1.0000
19:12147814:C:CTacceptor_gain1.0000
19:12147814:C:Tacceptor_gain1.0000
19:12147814:CACA:Cacceptor_gain1.0000
19:12147816:CA:Cacceptor_gain1.0000
19:12147817:A:Cacceptor_gain1.0000
19:12147819:G:Cacceptor_gain1.0000
19:12156553:CAC:Cdonor_loss1.0000
19:12156554:A:ACdonor_gain1.0000
19:12156554:AC:Adonor_gain1.0000
19:12156554:ACCA:Adonor_loss1.0000
19:12156554:ACCAT:Adonor_loss1.0000
19:12156555:C:Adonor_loss1.0000
19:12156555:C:CCdonor_gain1.0000
19:12156555:CC:Cdonor_gain1.0000
19:12156555:CCA:Cdonor_gain1.0000
19:12146220:GACCT:Gacceptor_gain0.9900
19:12146221:ACCTC:Aacceptor_loss0.9900
19:12146224:TCTGT:Tacceptor_loss0.9900

AlphaMissense

2472 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000235145 (19:12155969 GC>G,GCC), RS1000247500 (19:12150132 A>G,T), RS1000319240 (19:12149762 G>A), RS1000548840 (19:12147508 G>A), RS1000700716 (19:12154454 G>A), RS1000757280 (19:12154087 G>A), RS1000837389 (19:12154212 C>T), RS1001211295 (19:12150902 G>A), RS1001263635 (19:12150550 C>T), RS1001591273 (19:12149228 T>C), RS1001737016 (19:12155160 A>C), RS1001772156 (19:12157294 C>T), RS1002213567 (19:12149239 C>G,T), RS1002267696 (19:12148873 C>G,T), RS1002367101 (19:12156067 A>G)

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

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

13 total (human), top 13 by PubMed support.

ChemicalActions (top 5)PubMed papers
Phenylmercuric Acetateaffects cotreatment, decreases expression2
butyraldehydeincreases expression1
cupric oxideincreases expression1
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 Sincreases methylation1
Leflunomideincreases expression1
Atrazinedecreases expression1
Benzo(a)pyreneincreases methylation, decreases methylation1
Folic Aciddecreases expression1
Tobacco Smoke Pollutionincreases expression1
Urethaneincreases expression1
Acrylamideincreases 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.