ZNF775

gene
On this page

Also known as MGC33584

Summary

ZNF775 (zinc finger protein 775, HGNC:28501) is a protein-coding gene on chromosome 7q36.1, encoding Zinc finger protein 775 (Q96BV0). 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 transcription by RNA polymerase II. Predicted to be active in nucleus.

Source: NCBI Gene 285971 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 116 total
  • MANE Select transcript: NM_173680

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:28501
Approved symbolZNF775
Namezinc finger protein 775
Location7q36.1
Locus typegene with protein product
StatusApproved
AliasesMGC33584
Ensembl geneENSG00000196456
Ensembl biotypeprotein_coding
Entrez285971

Gene structure

Transcript identifiers

Ensembl transcripts: 16 — 16 protein_coding

ENST00000329630, ENST00000478789, ENST00000490973, ENST00000937963, ENST00000937964, ENST00000937965, ENST00000937966, ENST00000937967, ENST00000937968, ENST00000937969, ENST00000968864, ENST00000968865, ENST00000968866, ENST00000968867, ENST00000968868, ENST00000968869

RefSeq mRNA: 1 — MANE Select: NM_173680 NM_173680

CCDS: CCDS43678

Canonical transcript exons

ENST00000329630 — 3 exons

ExonStartEnd
ENSE00001330710150396513150398630
ENSE00001900789150379330150379392
ENSE00003863569150388422150388501

Expression profiles

Bgee: expression breadth ubiquitous, 196 present calls, max score 91.83.

FANTOM5 (CAGE): breadth broad, TPM avg 0.6655 / max 9.6722, expressed in 370 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
819365.07161602
819300.6655370

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
tendon of biceps brachiiUBERON:000818891.83gold quality
medial globus pallidusUBERON:000247787.60gold quality
globus pallidusUBERON:000187586.21gold quality
ganglionic eminenceUBERON:000402384.11gold quality
upper arm skinUBERON:000426383.97gold quality
ventricular zoneUBERON:000305382.94gold quality
buccal mucosa cellCL:000233682.93gold quality
cortical plateUBERON:000534381.77gold quality
mucosa of transverse colonUBERON:000499181.00gold quality
C1 segment of cervical spinal cordUBERON:000646980.88gold quality
cardiac muscle of right atriumUBERON:000337980.83gold quality
spinal cordUBERON:000224080.62gold quality
left ventricle myocardiumUBERON:000656680.33gold quality
inferior vagus X ganglionUBERON:000536380.18gold quality
lateral globus pallidusUBERON:000247679.86silver quality
ventral tegmental areaUBERON:000269179.65silver quality
putamenUBERON:000187479.30gold quality
transverse colonUBERON:000115779.22gold quality
subthalamic nucleusUBERON:000190678.89silver quality
substantia nigraUBERON:000203878.84gold quality
muscle layer of sigmoid colonUBERON:003580578.84gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099178.83gold quality
midbrainUBERON:000189178.81gold quality
vena cavaUBERON:000408778.68gold quality
lower esophagus muscularis layerUBERON:003583378.58gold quality
lower esophagusUBERON:001347378.53gold quality
dorsal plus ventral thalamusUBERON:000189778.52silver quality
substantia nigra pars reticulataUBERON:000196678.42gold quality
prefrontal cortexUBERON:000045178.41gold quality
body of tongueUBERON:001187678.10gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.93

Regulation

Is transcription factor: yes

JASPAR motifs

MotifNameFamily
MA2531.1ZNF775Factors with multiple dispersed zinc fingers

JASPAR matrix evidence (PMIDs): PMID:39605320

miRNA regulators (miRDB)

4 targeting ZNF775, 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-532-3P99.3465.761195
HSA-MIR-4667-3P99.2665.451608
HSA-MIR-129196.2865.891224
HSA-MIR-6775-3P95.7665.91982

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
mus_musculusZfp719ENSMUSG00000030469
mus_musculusZfp141ENSMUSG00000092416
mus_musculusB020011L13RikENSMUSG00000101303
drosophila_melanogasterMeicsFBGN0025874

Paralogs (176): ZNF195 (ENSG00000005801), ZNF112 (ENSG00000062370), ZNF275 (ENSG00000063587), ZNF37A (ENSG00000075407), ZNF510 (ENSG00000081386), ZNF506 (ENSG00000081665), ZNF268 (ENSG00000090612), MZF1 (ENSG00000099326), ZNF629 (ENSG00000102870), ZNF175 (ENSG00000105497), ZNF85 (ENSG00000105750), ZFP30 (ENSG00000120784), ZNF45 (ENSG00000124459), ZNF391 (ENSG00000124613), ZNF436 (ENSG00000125945), ZNF484 (ENSG00000127081), ZNF835 (ENSG00000127903), ZNF780B (ENSG00000128000), ZSCAN10 (ENSG00000130182), ZNF317 (ENSG00000130803), ZNF331 (ENSG00000130844), ZNF227 (ENSG00000131115), ZNF141 (ENSG00000131127), ZNF132 (ENSG00000131849), ZNF189 (ENSG00000136870), ZIM3 (ENSG00000141946), ZFP14 (ENSG00000142065), ZNF514 (ENSG00000144026), ZNF300 (ENSG00000145908), RBAK (ENSG00000146587), ZNF157 (ENSG00000147117), ZNF182 (ENSG00000147118), ZNF41 (ENSG00000147124), ZNF7 (ENSG00000147789), ZNF117 (ENSG00000152926), ZNF221 (ENSG00000159905), ZNF235 (ENSG00000159917), ZNF714 (ENSG00000160352), ZNF577 (ENSG00000161551), ZNF12 (ENSG00000164631)

Protein

Protein identifiers

Zinc finger protein 775Q96BV0 (reviewed: Q96BV0)

All UniProt accessions (3): C9JAM7, C9JVG2, Q96BV0

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_775951* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR013087Znf_C2H2_typeDomain
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096

UniProt features (18 total): zinc finger region 11, region of interest 2, compositionally biased region 2, chain 1, cross-link 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96BV0-F163.770.00

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): 533

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 78 (showing top): GSE45365_NK_CELL_VS_CD8A_DC_MCMV_INFECTION_DN, GSE18804_BRAIN_VS_COLON_TUMORAL_MACROPHAGE_DN, TGACCTY_ERR1_Q2, CACCAGC_MIR138, CCATCCA_MIR432, LEF1_Q6, OSF2_Q6, YOSHIMURA_MAPK8_TARGETS_DN, TCANNTGAY_SREBP1_01, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, PR_01, KOYAMA_SEMA3B_TARGETS_DN, ZWANG_TRANSIENTLY_UP_BY_2ND_EGF_PULSE_ONLY, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ARID5B_TARGET_GENES

GO Biological Process (1): regulation of transcription by RNA polymerase II (GO:0006357)

GO Molecular Function (7): 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 factor activity (GO:0003700), 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 transcription2
RNA polymerase II transcription regulatory region sequence-specific DNA binding2
transcription by RNA polymerase II1
cis-regulatory region sequence-specific DNA binding1
chromatin1
DNA-binding transcription factor activity1
regulation of transcription by RNA polymerase II1
transcription cis-regulatory region binding1
transcription regulator activity1
transition metal ion binding1
nucleic acid binding1
binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

500 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF775GIMAP8Q8ND71507
ZNF775GIMAP2Q9UG22500
ZNF775A0A087WTJ2A0A087WTJ2493
ZNF775GIMAP7Q8NHV1483
ZNF775TMEM176BQ3YBM2482
ZNF775SYCE1LA8MT33450
ZNF775GIMAP6Q6P9H5449
ZNF775C7orf33Q8WU49448
ZNF775DRC11LA6NCM1445
ZNF775GIMAP5Q96F15440
ZNF775TMEM120AQ9BXJ8425
ZNF775URB2Q14146400
ZNF775ZBED10PQ96FA7398
ZNF775DENND2CQ68D51385
ZNF775TTLL8A6PVC2381

IntAct

45 interactions, top by confidence:

ABTypeScore
ZNF775ZRANB1psi-mi:“MI:0915”(physical association)0.560
CEP70ZNF775psi-mi:“MI:0915”(physical association)0.560
KRTAP10-8ZNF775psi-mi:“MI:0915”(physical association)0.560
ZNF775CARD10psi-mi:“MI:0915”(physical association)0.560
ZNF775EHMT2psi-mi:“MI:0915”(physical association)0.560
CYSRT1ZNF775psi-mi:“MI:0915”(physical association)0.560
MTUS2ZNF775psi-mi:“MI:0915”(physical association)0.560
ZNF775TSPYL2psi-mi:“MI:0915”(physical association)0.560
DVL3ZNF775psi-mi:“MI:0915”(physical association)0.560
FAM9AZNF775psi-mi:“MI:0915”(physical association)0.560
CACNG5ZNF316psi-mi:“MI:0914”(association)0.530
ZNF775DAP3psi-mi:“MI:0915”(physical association)0.400
FESZNF775psi-mi:“MI:0915”(physical association)0.370
ZNF775MAPK6psi-mi:“MI:0915”(physical association)0.370
OSGEPZNF775psi-mi:“MI:0915”(physical association)0.370
PPP2CBZNF775psi-mi:“MI:0915”(physical association)0.370
ZNF775RPS6KA5psi-mi:“MI:0915”(physical association)0.370
MAP3K20ZNF775psi-mi:“MI:0915”(physical association)0.370
NOTCH2ZNF320psi-mi:“MI:0914”(association)0.350
LTBP2ZNF320psi-mi:“MI:0914”(association)0.350
PTX3POLRMTpsi-mi:“MI:0914”(association)0.350
TRIM63ZNF775psi-mi:“MI:0915”(physical association)0.000
TRIM55ZNF775psi-mi:“MI:0915”(physical association)0.000
ZNF775ZRANB1psi-mi:“MI:0915”(physical association)0.000
ZNF775CEP70psi-mi:“MI:0915”(physical association)0.000
ZNF775KRTAP10-8psi-mi:“MI:0915”(physical association)0.000
ZNF775CARD10psi-mi:“MI:0915”(physical association)0.000
ZNF775TSPYL2psi-mi:“MI:0915”(physical association)0.000

BioGRID (28): ZNF775 (Affinity Capture-MS), ZNF775 (Affinity Capture-MS), ZNF775 (Two-hybrid), ZNF775 (Two-hybrid), ZNF775 (Two-hybrid), ZNF775 (Two-hybrid), ZNF775 (Two-hybrid), ZNF775 (Two-hybrid), ZNF775 (Two-hybrid), ZNF775 (Two-hybrid), CYSRT1 (Two-hybrid), EHMT2 (Two-hybrid), ZNF775 (Proximity Label-MS), ZNF775 (Two-hybrid), ZNF775 (Two-hybrid)

ESM2 similar proteins: A3KN32, A6NM28, A8K8V0, E9PYI1, O75467, O95201, P10072, P10075, P10078, P10754, P28698, P30373, P52736, Q0VCC5, Q14929, Q16587, Q17QR7, Q29RZ4, Q3KNW1, Q3TDE8, Q3US17, Q58DK7, Q5RJR4, Q5T619, Q5TEC3, Q5U4E2, Q62396, Q68H95, Q6AW86, Q6PGE4, Q6ZMY9, Q7Z398, Q7Z7K2, Q8BI73, Q8BIF9, Q8BIQ3, Q8BKK5, Q8JZL0, Q8N393, Q8R0T2

Diamond homologs: P17041, P18732, Q08AN1, Q3US17, Q80V23, Q86T29, Q8CF60, Q8TBZ5, Q96BV0, Q96EG3, Q9H4T2, Q9H7R5, Q9HAH1, O15090, O43167, P18744, P18747, Q5EBL2, Q62255, Q80X44, Q8CJ78, Q8K083, Q9BXA9, Q9ER74, Q9NSC2, Q9UDV7, B0K011, P23803, P41995, P60319, P86413, Q08DS3, Q0IHB8, Q32NK7, Q3T135, Q567J8, Q5XJQ7, Q66JF8, Q6AY34, Q7PN68

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance110
Likely benign5
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1407 predictions. Top by Δscore:

VariantEffectΔscore
7:150396501:T:Aacceptor_gain1.0000
7:150396507:T:TAacceptor_gain1.0000
7:150368937:CAGAG:Cdonor_loss0.9900
7:150368938:AGAGG:Adonor_loss0.9900
7:150368939:GAG:Gdonor_gain0.9900
7:150368940:AGGT:Adonor_loss0.9900
7:150368941:GGTA:Gdonor_loss0.9900
7:150368942:GTAC:Gdonor_loss0.9900
7:150368943:T:Adonor_loss0.9900
7:150369867:GG:Gdonor_gain0.9900
7:150369868:GG:Gdonor_gain0.9900
7:150369869:G:Tdonor_gain0.9900
7:150370349:G:GTdonor_gain0.9900
7:150371226:A:AGacceptor_gain0.9900
7:150371227:G:GGacceptor_gain0.9900
7:150371227:GCA:Gacceptor_gain0.9900
7:150379387:TCAA:Tdonor_gain0.9900
7:150379388:CAAAG:Cdonor_loss0.9900
7:150379390:AAGGT:Adonor_loss0.9900
7:150379392:GGTAT:Gdonor_loss0.9900
7:150379394:T:Gdonor_loss0.9900
7:150396497:C:CAacceptor_gain0.9900
7:150396508:G:Aacceptor_gain0.9900
7:150396509:GCAG:Gacceptor_loss0.9900
7:150396510:CAG:Cacceptor_loss0.9900
7:150396512:G:GTacceptor_loss0.9900
7:150396512:GGA:Gacceptor_gain0.9900
7:150369800:G:GTdonor_gain0.9800
7:150394454:T:TAacceptor_gain0.9800
7:150396511:A:AGacceptor_gain0.9800

AlphaMissense

3475 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
7:150396827:T:CF116L1.000
7:150396829:C:AF116L1.000
7:150396829:C:GF116L1.000
7:150397844:T:CF455L1.000
7:150397846:C:AF455L1.000
7:150397846:C:GF455L1.000
7:150397928:T:CF483L1.000
7:150397930:C:AF483L1.000
7:150397930:C:GF483L1.000
7:150396854:C:GH125D0.999
7:150396911:T:CF144L0.999
7:150396913:C:AF144L0.999
7:150396913:C:GF144L0.999
7:150396995:T:CF172L0.999
7:150396997:C:AF172L0.999
7:150396997:C:GF172L0.999
7:150397349:T:CF290L0.999
7:150397350:T:CF290S0.999
7:150397351:C:AF290L0.999
7:150397351:C:GF290L0.999
7:150397376:C:GH299D0.999
7:150397433:T:CF318L0.999
7:150397434:T:CF318S0.999
7:150397435:C:AF318L0.999
7:150397435:C:GF318L0.999
7:150397517:T:CF346L0.999
7:150397519:C:AF346L0.999
7:150397519:C:GF346L0.999
7:150397871:C:GH464D0.999
7:150397929:T:CF483S0.999

dbSNP variants (sampled 300 via entrez): RS1000213400 (7:150388546 C>T), RS1000265621 (7:150388268 A>G), RS1000375585 (7:150382803 C>T), RS1000786037 (7:150386171 G>A), RS1000827637 (7:150381804 C>T), RS1000930555 (7:150380249 G>A,C), RS1001037010 (7:150391405 G>A), RS1001114317 (7:150381414 T>A), RS1001248142 (7:150398745 G>A), RS1001278147 (7:150385156 G>A,T), RS1001305243 (7:150398455 G>A), RS1001490193 (7:150390384 C>T), RS1001737832 (7:150381546 G>A,C), RS1001832999 (7:150391488 A>G), RS1001864169 (7:150395071 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

1 associations (top):

StudyTraitp-value
GCST004765_15Total cholesterol change in response to fenofibrate in statin-treated type 2 diabetes2.000000e-07

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0007806total cholesterol change measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

27 total (human), top 27 by PubMed support.

ChemicalActions (top 5)PubMed papers
Phenylmercuric Acetateaffects cotreatment, decreases expression2
Smokedecreases expression, increases abundance, increases expression2
FR900359increases phosphorylation1
TAK-243increases sumoylation1
beta-lapachonedecreases expression1
sodium arsenitedecreases expression1
benzo(e)pyreneincreases methylation1
di-n-butylphosphoric acidaffects expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
ICG 001decreases expression1
abrineincreases expression1
dorsomorphinaffects cotreatment, decreases expression1
jinfukangincreases expression1
Resveratroldecreases expression, affects cotreatment1
Zoledronic Acidincreases expression1
Air Pollutantsincreases expression, increases abundance1
Cadmiumdecreases expression, increases abundance1
Cisplatindecreases expression1
Dexamethasoneaffects cotreatment, decreases expression1
Methapyrileneincreases methylation1
Plant Extractsdecreases expression, affects cotreatment1
Tobacco Smoke Pollutiondecreases expression1
Urethaneincreases expression1
Valproic Aciddecreases expression1
Cadmium Chloridedecreases expression, increases abundance1
Copper Sulfatedecreases expression1
Genisteinaffects cotreatment, decreases 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.