ZNF177

gene
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Summary

ZNF177 (zinc finger protein 177, HGNC:12966) is a protein-coding gene on chromosome 19p13.2, encoding Zinc finger protein 177 (Q13360). May be involved in transcriptional regulation.

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in blood microparticle.

Source: NCBI Gene 7730 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 36 total
  • MANE Select transcript: NM_001172651

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:12966
Approved symbolZNF177
Namezinc finger protein 177
Location19p13.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000188629
Ensembl biotypeprotein_coding
OMIM601276
Entrez7730

Gene structure

Transcript identifiers

Ensembl transcripts: 7 — 7 protein_coding

ENST00000343499, ENST00000589262, ENST00000590616, ENST00000592912, ENST00000683217, ENST00000888362, ENST00000920310

RefSeq mRNA: 4 — MANE Select: NM_001172651 NM_001172651, NM_001384658, NM_001384659, NM_003451

CCDS: CCDS54214

Canonical transcript exons

ENST00000683217 — 8 exons

ExonStartEnd
ENSE0000345959593763169376423
ENSE0000347020193782599378344
ENSE0000347961493648629364948
ENSE0000349351193789629379088
ENSE0000353380593800579380139
ENSE0000354767493795279379619
ENSE0000391674493806689382617
ENSE0000391948993630139363084

Expression profiles

Bgee: expression breadth ubiquitous, 133 present calls, max score 89.62.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.3452 / max 14.3536, expressed in 166 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1736960.3452166

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099189.62gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047386.02gold quality
right uterine tubeUBERON:000130283.87gold quality
cerebellar hemisphereUBERON:000224580.20gold quality
corpus callosumUBERON:000233680.10gold quality
cerebellar cortexUBERON:000212980.04gold quality
cerebellumUBERON:000203779.91gold quality
right hemisphere of cerebellumUBERON:001489079.74gold quality
right testisUBERON:000453479.28gold quality
ventricular zoneUBERON:000305378.82gold quality
testisUBERON:000047378.78gold quality
left testisUBERON:000453378.66gold quality
amygdalaUBERON:000187677.95gold quality
temporal lobeUBERON:000187177.77gold quality
ganglionic eminenceUBERON:000402377.70gold quality
left ovaryUBERON:000211977.66gold quality
cortical plateUBERON:000534377.59gold quality
Ammon’s hornUBERON:000195477.42gold quality
right ovaryUBERON:000211877.38gold quality
caudate nucleusUBERON:000187377.29gold quality
nucleus accumbensUBERON:000188277.20gold quality
ovaryUBERON:000099277.17gold quality
apex of heartUBERON:000209877.13gold quality
substantia nigraUBERON:000203877.12gold quality
C1 segment of cervical spinal cordUBERON:000646977.11gold quality
brainUBERON:000095576.84gold quality
hypothalamusUBERON:000189876.66gold quality
body of uterusUBERON:000985376.56gold quality
putamenUBERON:000187476.50gold quality
pituitary glandUBERON:000000776.49gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.36

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

69 targeting ZNF177, 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-5193100.0067.261744
HSA-MIR-188-3P100.0068.761240
HSA-MIR-4789-3P99.9970.752484
HSA-MIR-6891-5P99.9866.531372
HSA-MIR-365899.9673.874379
HSA-MIR-314399.9371.963104
HSA-MIR-497-5P99.9271.832674
HSA-MIR-454-3P99.9174.011925
HSA-MIR-15A-5P99.9072.802787
HSA-MIR-15B-5P99.9072.782798
HSA-MIR-16-5P99.9072.802780
HSA-MIR-195-5P99.9072.812805
HSA-MIR-130A-3P99.9073.311861
HSA-MIR-130B-3P99.9073.271850
HSA-MIR-301A-3P99.9073.151839
HSA-MIR-301B-3P99.9073.191836
HSA-MIR-366699.9073.241833
HSA-MIR-429599.9073.111838
HSA-MIR-424-5P99.8971.902641
HSA-MIR-6838-5P99.8971.942690
HSA-MIR-4671-3P99.8872.461045
HSA-MIR-7845-5P99.8864.88771
HSA-MIR-132199.8465.301811
HSA-MIR-473999.8465.251832
HSA-MIR-4756-5P99.8464.981809
HSA-MIR-139-5P99.8069.501399
HSA-MIR-548AU-3P99.7068.221373
HSA-MIR-472999.6972.184233
HSA-MIR-379-3P99.6969.601524
HSA-MIR-411-3P99.6969.631524

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
drosophila_melanogasterCG2712FBGN0024975
drosophila_melanogasterPhsFBGN0036522
drosophila_melanogasterCG3281FBGN0260741

Paralogs (62): ZNF582 (ENSG00000018869), ZNF264 (ENSG00000083844), ZNF343 (ENSG00000088876), ZNF684 (ENSG00000117010), ZNF133 (ENSG00000125846), ZNF557 (ENSG00000130544), ZNF337 (ENSG00000130684), ZNF20 (ENSG00000132010), ZFP37 (ENSG00000136866), ZNF614 (ENSG00000142556), KRBOX4 (ENSG00000147121), ZNF599 (ENSG00000153896), ZNF19 (ENSG00000157429), ZNF589 (ENSG00000164048), PRDM9 (ENSG00000164256), ZNF180 (ENSG00000167384), ZNF558 (ENSG00000167785), ZNF35 (ENSG00000169981), ZNF778 (ENSG00000170100), ZNF439 (ENSG00000171291), ZNF440 (ENSG00000171295), ZNF556 (ENSG00000172000), ZNF554 (ENSG00000172006), ZNF596 (ENSG00000172748), ZNF80 (ENSG00000174255), ZNF266 (ENSG00000174652), ZNF25 (ENSG00000175395), ZNF77 (ENSG00000175691), ZNF169 (ENSG00000175787), ZNF404 (ENSG00000176222), ZNF491 (ENSG00000177599), ZNF620 (ENSG00000177842), ZNF619 (ENSG00000177873), ZNF875 (ENSG00000181666), ZNF329 (ENSG00000181894), ZFP90 (ENSG00000184939), ZNF566 (ENSG00000186017), ZNF529 (ENSG00000186020), ZNF749 (ENSG00000186230), ZNF555 (ENSG00000186300)

Protein

Protein identifiers

Zinc finger protein 177Q13360 (reviewed: Q13360)

All UniProt accessions (3): Q13360, K7EK36, K7EQU1

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?
Q13360-11yes
Q13360-22
Q13360-33

RefSeq proteins (4): NP_001166122, NP_001371587, NP_001371588, NP_003442 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050752C2H2-ZF_domainFamily

Pfam: PF00096, PF01352, PF13465, PF13912

UniProt features (20 total): zinc finger region 10, splice variant 3, sequence variant 3, sequence conflict 2, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q13360-F161.420.25

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 60 (showing top): SHEDDEN_LUNG_CANCER_GOOD_SURVIVAL_A5, MORF_ZNF10, MODULE_123, MORF_EPHA7, BROWNE_HCMV_INFECTION_10HR_UP, DEURIG_T_CELL_PROLYMPHOCYTIC_LEUKEMIA_UP, MORF_DCC, NUYTTEN_EZH2_TARGETS_DN, GOCC_BLOOD_MICROPARTICLE, chr19p13, MORF_FRK, GAZDA_DIAMOND_BLACKFAN_ANEMIA_ERYTHROID_DN, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, HATADA_METHYLATED_IN_LUNG_CANCER_UP, GOBP_NEGATIVE_REGULATION_OF_TRANSCRIPTION_BY_RNA_POLYMERASE_II

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

GO Molecular Function (7): 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), sequence-specific double-stranded DNA binding (GO:1990837), DNA binding (GO:0003677), protein binding (GO:0005515), metal ion binding (GO:0046872)

GO Cellular Component (2): nucleus (GO:0005634), blood microparticle (GO:0072562)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
regulation of transcription by RNA polymerase II2
transcription by RNA polymerase II2
negative regulation of DNA-templated transcription1
regulation of DNA-templated transcription1
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
transition metal ion binding1
double-stranded DNA binding1
sequence-specific DNA binding1
nucleic acid binding1
binding1
cation binding1
intracellular membrane-bounded organelle1
extracellular region1
cellular anatomical structure1

Protein interactions and networks

STRING

400 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF177SHKBP1Q8TBC3925
ZNF177CDO1P78513581
ZNF177BCAT1P54687571
ZNF177TRIM58Q8NG06570
ZNF177OR6S1Q8NH40474
ZNF177SLC27A5Q9Y2P5412
ZNF177CPXM1Q96SM3399
ZNF177DEPDC4Q8N2C3396
ZNF177ANKRD53Q8N9V6395
ZNF177FSD1Q9BTV5366
ZNF177ZC3H6P61129329
ZNF177CCDC184Q52MB2311
ZNF177DPYSL4O14531306
ZNF177ADCY4Q8NFM4305
ZNF177CLXNQ9HAE3301
ZNF177CCDC181Q5TID7301

IntAct

8 interactions, top by confidence:

ABTypeScore
ZNF177ARHGAP21psi-mi:“MI:0915”(physical association)0.560
ARHGAP21ZNF177psi-mi:“MI:0915”(physical association)0.560
ZNF177CANXpsi-mi:“MI:0915”(physical association)0.400
ZNF177psi-mi:“MI:0915”(physical association)0.370
SLC37A3ZNF177psi-mi:“MI:0915”(physical association)0.370
Cdca5ATP5MF-PTCD1psi-mi:“MI:0914”(association)0.350

BioGRID (41): ARHGAP21 (Two-hybrid), ZNF177 (Affinity Capture-MS), ZNF177 (Reconstituted Complex), ZNF177 (Two-hybrid), ZNF559-ZNF177 (Two-hybrid), ZNF177 (Two-hybrid), ZNF559-ZNF177 (Two-hybrid), ZNF177 (Two-hybrid), ZNF559-ZNF177 (Two-hybrid), ZNF177 (Two-hybrid), ZNF559-ZNF177 (Two-hybrid), ZNF177 (Two-hybrid), ZNF559-ZNF177 (Two-hybrid), ZNF177 (Two-hybrid), ZNF559-ZNF177 (Two-hybrid)

ESM2 similar proteins: A0A1W2PQL4, A0JPL0, A2RRD8, A6NHJ4, A6NP11, B4DX44, O75346, O95780, P0CB33, P21506, P51508, P52738, Q0D2J5, Q0VGE8, Q12901, Q13360, Q14593, Q15973, Q2M218, Q2M3X9, Q2VY69, Q3SXZ3, Q5HY98, Q5RCJ2, Q5VIY5, Q6J6I6, Q7L2R6, Q86XU0, Q86Y25, Q8IW36, Q8IYN0, Q8IYX0, Q8N782, Q8N883, Q8N9Z0, Q8NDP4, Q95K49, Q969W8, Q96H40, Q96N58

Diamond homologs: A0A1W2PQL4, A0JNB1, A0JPL0, A6NK53, A6QLU5, A6QPT6, A7MBI1, A8MT65, A8MUV8, A8MWA4, B2RXC5, B4DU55, B4DX44, E9PYI1, O14628, O75346, P0CH99, P0CI00, P17014, P17030, P17032, P17098, P51786, P85977, Q02386, Q06730, Q06732, Q0VAW7, Q12901, Q13360, Q14586, Q14588, Q14590, Q16587, Q2M3X9, Q2VY69, Q32M78, Q3ZCX4, Q49AA0, Q4R6J4

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 significance34
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1880 predictions. Top by Δscore:

VariantEffectΔscore
19:9379504:A:AGacceptor_gain1.0000
19:9379505:T:Gacceptor_gain1.0000
19:9379516:T:Aacceptor_gain1.0000
19:9379518:C:CAacceptor_gain1.0000
19:9379525:AG:Aacceptor_gain1.0000
19:9379525:AGG:Aacceptor_gain1.0000
19:9379526:GG:Gacceptor_gain1.0000
19:9379526:GGG:Gacceptor_gain1.0000
19:9364475:GGAA:Gdonor_gain0.9900
19:9364476:G:Tdonor_gain0.9900
19:9364856:TTTCA:Tacceptor_loss0.9900
19:9364857:TTCA:Tacceptor_loss0.9900
19:9364858:TCA:Tacceptor_loss0.9900
19:9364859:CAGGG:Cacceptor_loss0.9900
19:9364860:A:AGacceptor_gain0.9900
19:9364860:A:ATacceptor_loss0.9900
19:9364860:AG:Aacceptor_gain0.9900
19:9364861:G:GGacceptor_gain0.9900
19:9364861:GG:Gacceptor_gain0.9900
19:9364861:GGGCT:Gacceptor_gain0.9900
19:9364947:GG:Gdonor_gain0.9900
19:9364948:GG:Gdonor_gain0.9900
19:9378257:A:AGacceptor_gain0.9900
19:9378258:G:GGacceptor_gain0.9900
19:9378339:TCAC:Tdonor_gain0.9900
19:9379503:C:Gacceptor_gain0.9900
19:9379509:T:Aacceptor_gain0.9900
19:9379520:T:TAacceptor_gain0.9900
19:9379524:CAGGG:Cacceptor_loss0.9900
19:9379525:A:AGacceptor_gain0.9900

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000102397 (19:9362998 C>T), RS1000181985 (19:9379328 G>A), RS1000316701 (19:9379276 T>C), RS1000485563 (19:9380641 A>C,G), RS1000604933 (19:9379515 C>T), RS1000875858 (19:9369205 CT>C,CTT), RS1000926289 (19:9368952 C>T), RS1001023952 (19:9375079 C>T), RS1001246311 (19:9369655 C>T), RS1001297259 (19:9370122 A>G), RS1001312006 (19:9362791 C>A,G), RS1001432279 (19:9376117 T>C), RS1001772375 (19:9363355 T>C), RS1002116597 (19:9365277 T>G), RS1002149985 (19:9381898 G>T)

Disease associations

OMIM: gene MIM:601276 | 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

18 total (human), top 18 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects cotreatment, decreases expression, affects expression5
fluorene-9-bisphenolincreases expression1
tris(1,3-dichloro-2-propyl)phosphateincreases expression1
CGP 52608affects binding, increases reaction1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
dorsomorphindecreases expression, affects cotreatment1
Decitabineincreases expression1
Benzo(a)pyreneaffects methylation, decreases methylation1
Cisplatindecreases expression1
Formaldehydeincreases expression1
Leadincreases expression1
Methyl Methanesulfonateincreases expression1
Nickeldecreases expression1
Phenylmercuric Acetateaffects cotreatment, decreases expression1
Cyclosporineincreases expression1
Aflatoxin B1increases methylation1
Genisteinincreases 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.