ZNF705G

gene
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Summary

ZNF705G (zinc finger protein 705G, HGNC:37134) is a protein-coding gene on chromosome 8p23.1, encoding Putative zinc finger protein 705G (A8MUZ8). 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 100131980 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 91 total
  • MANE Select transcript: NM_001164457

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:37134
Approved symbolZNF705G
Namezinc finger protein 705G
Location8p23.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000215372
Ensembl biotypeprotein_coding
Entrez100131980

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000400156

RefSeq mRNA: 1 — MANE Select: NM_001164457 NM_001164457

CCDS: CCDS47773

Canonical transcript exons

ENST00000400156 — 7 exons

ExonStartEnd
ENSE0000162116473814527381601
ENSE0000164734873596197359701
ENSE0000166310073611107361236
ENSE0000168197273854987385558
ENSE0000177487373602377360332
ENSE0000179354373629357363017
ENSE0000217119473555177358560

Expression profiles

Bgee: expression breadth tissue_specific, 3 present calls, max score 40.27.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548840.27gold quality
right testisUBERON:000453437.57gold quality
ganglionic eminenceUBERON:000402337.22gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
left testisUBERON:000453335.78gold quality
testisUBERON:000047335.70gold quality
skeletal muscle tissueUBERON:000113434.95gold quality
muscle tissueUBERON:000238533.31gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
monocyteCL:000057632.13gold quality
bone marrowUBERON:000237131.74gold quality
mucosa of stomachUBERON:000119931.73gold quality
leukocyteCL:000073831.72gold quality
prefrontal cortexUBERON:000045130.27gold quality
stromal cell of endometriumCL:000225529.87gold quality
right uterine tubeUBERON:000130229.21gold quality
tonsilUBERON:000237228.60gold quality
liverUBERON:000210728.29gold quality
duodenumUBERON:000211428.14gold quality
urinary bladderUBERON:000125527.59gold quality
lymph nodeUBERON:000002927.57gold quality
primary visual cortexUBERON:000243627.42gold quality
smooth muscle tissueUBERON:000113527.38gold quality
olfactory segment of nasal mucosaUBERON:000538627.32gold quality
bloodUBERON:000017827.07gold quality
corpus callosumUBERON:000233627.06gold quality
islet of LangerhansUBERON:000000626.55gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.63

Regulation

Is transcription factor: no

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
mus_musculusZfp78ENSMUSG00000055150
rattus_norvegicusENSRNOG00000083797
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

Putative zinc finger protein 705GA8MUZ8 (reviewed: A8MUZ8)

All UniProt accessions (1): A8MUZ8

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_001157929* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (6 total): zinc finger region 4, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A8MUZ8-F167.400.15

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 24 (showing top): GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_MCMV_INFECTION_DN, GSE45365_NK_CELL_VS_CD8A_DC_MCMV_INFECTION_UP, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, GOMF_DNA_BINDING_TRANSCRIPTION_FACTOR_ACTIVITY, GSE26928_NAIVE_VS_EFF_MEMORY_CD4_TCELL_UP, GSE26928_NAIVE_VS_CXCR5_POS_CD4_TCELL_UP, GOMF_RNA_POLYMERASE_II_TRANSCRIPTION_REGULATORY_REGION_SEQUENCE_SPECIFIC_DNA_BINDING, GSE2770_IL12_AND_TGFB_VS_IL4_TREATED_ACT_CD4_TCELL_2H_DN, GSE1112_OT1_CD8AB_VS_HY_CD8AA_THYMOCYTE_RTOC_CULTURE_UP, GSE1740_UNSTIM_VS_IFNA_STIMULATED_MCSF_DERIVED_MACROPHAGE_UP, GSE1791_CTRL_VS_NEUROMEDINU_IN_T_CELL_LINE_0.8H_UP, GSE1791_CTRL_VS_NEUROMEDINU_IN_T_CELL_LINE_12H_DN, chr8p23, GSE18281_PERIMEDULLARY_CORTICAL_REGION_VS_WHOLE_MEDULLA_THYMUS_DN

GO Biological Process (2): regulation of transcription by RNA polymerase II (GO:0006357), regulation of DNA-templated transcription (GO:0006355)

GO Molecular Function (5): 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), 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
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

84 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF705GSPATA31A6Q5VVP1599
ZNF705GANKRD20A4PQ4UJ75581
ZNF705GENPP7Q6UWV6541
ZNF705GBET1LQ9NYM9380
ZNF705GDNAJC8O75937377
ZNF705GLRRC37A3O60309374
ZNF705GEME2A4GXA9367
ZNF705GWDR3Q9UNX4348
ZNF705GCETN1Q12798269
ZNF705GSF3B3Q15393245
ZNF705GCETN2P41208212
ZNF705GIARS1P41252211
ZNF705GTNKSO95271203
ZNF705GHLA-DQA2P01906160
ZNF705GHLA-DQB1P01917145

IntAct

0 interactions, top by confidence:

BioGRID (2): CCT8 (Cross-Linking-MS (XL-MS)), ZNF705G (Reconstituted Complex)

ESM2 similar proteins: A0A2K5V015, A1YIY0, A8MUZ8, A8MWA4, B8JI71, O08569, P01133, P0DJ43, P14370, P14585, P17630, P19070, P48357, P82279, P97435, Q07444, Q0D2K5, Q28066, Q28660, Q29RU2, Q4KUS1, Q5G872, Q5R6R1, Q5RCW9, Q5T1H1, Q5UKY4, Q5Z5Q3, Q60736, Q63515, Q63722, Q6DFV8, Q6GMZ9, Q6V0K7, Q6ZN79, Q7TSY4, Q811Q4, Q8N2E2, Q8VHS2, Q90Y54, Q95MI4

Diamond homologs: A0JPL0, A2VDP4, A6QLU5, A6QPT6, A8MQ14, A8MUZ8, A8MWA4, B1APH4, B2RXC5, E9PYI1, E9Q8G5, O75290, O94892, P08042, P0CH99, P0CI00, P17014, P17025, P17030, P17031, P17032, P17098, P21506, P51508, P51523, P51786, P51814, P52736, P52738, Q02525, Q03923, Q03936, Q06730, Q06732, Q0VCB0, Q13401, Q14587, Q16587, Q2M218, Q2M3X9

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance82
Likely benign7
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

981 predictions. Top by Δscore:

VariantEffectΔscore
8:7359612:AACTT:Adonor_loss1.0000
8:7359613:ACTTA:Adonor_loss1.0000
8:7359614:CTTAC:Cdonor_loss1.0000
8:7359615:TTACC:Tdonor_loss1.0000
8:7359616:TAC:Tdonor_loss1.0000
8:7359617:A:ACdonor_gain1.0000
8:7359618:C:CCdonor_gain1.0000
8:7359698:CTGT:Cacceptor_gain1.0000
8:7359699:TGTC:Tacceptor_loss1.0000
8:7359711:T:TCacceptor_gain1.0000
8:7360235:A:ACdonor_gain1.0000
8:7360236:C:CCdonor_gain1.0000
8:7361103:GACTC:Gdonor_loss1.0000
8:7361104:ACTCA:Adonor_loss1.0000
8:7361105:CTCAC:Cdonor_loss1.0000
8:7361106:TCA:Tdonor_loss1.0000
8:7361107:CACCG:Cdonor_loss1.0000
8:7361108:A:ACdonor_gain1.0000
8:7361108:ACCGA:Adonor_loss1.0000
8:7361109:C:CAdonor_gain1.0000
8:7361232:TTCTT:Tacceptor_gain1.0000
8:7361234:CTT:Cacceptor_gain1.0000
8:7361237:C:CCacceptor_gain1.0000
8:7359617:AC:Adonor_gain0.9900
8:7359618:CC:Cdonor_gain0.9900
8:7359618:CCA:Cdonor_gain0.9900
8:7359699:TGT:Tacceptor_gain0.9900
8:7359700:GT:Gacceptor_gain0.9900
8:7359702:C:CCacceptor_gain0.9900
8:7359711:T:Cacceptor_gain0.9900

AlphaMissense

2010 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
8:7358252:G:CF209L0.977
8:7358252:G:TF209L0.977
8:7358254:A:GF209L0.977
8:7361121:A:GL43P0.964
8:7361202:A:GF16S0.964
8:7358000:G:CF293L0.954
8:7358000:G:TF293L0.954
8:7358002:A:GF293L0.954
8:7361201:G:CF16L0.954
8:7361201:G:TF16L0.954
8:7361203:A:GF16L0.954
8:7361155:A:CY32D0.945
8:7361188:A:GW21R0.945
8:7361188:A:TW21R0.945
8:7361139:A:GL37P0.944
8:7361186:C:AW21C0.943
8:7361186:C:GW21C0.943
8:7361212:C:GA13P0.941
8:7361222:A:CF9L0.932
8:7361222:A:TF9L0.932
8:7361224:A:GF9L0.932
8:7358168:A:CF237L0.924
8:7358168:A:TF237L0.924
8:7358170:A:GF237L0.924
8:7361162:T:AR29S0.914
8:7361162:T:GR29S0.914
8:7358313:C:GR189P0.907
8:7361142:A:GM36T0.904
8:7361136:T:AE38V0.902
8:7361132:A:CN39K0.886

dbSNP variants (sampled 300 via entrez): RS1000241593 (8:7385269 A>C), RS1000260179 (8:7365646 A>C,T), RS1000396493 (8:7366297 G>A,T), RS1000651979 (8:7387276 G>A,T), RS1000696810 (8:7385720 C>G,T), RS1000888004 (8:7356899 G>A), RS1001931488 (8:7362771 C>A,T), RS1001961199 (8:7382170 C>T), RS1002067415 (8:7363152 A>C), RS1002310736 (8:7380783 G>A,C), RS1002598813 (8:7357049 T>A), RS1002631886 (8:7369930 T>A,C,G), RS1002734777 (8:7357528 T>A), RS1002920113 (8:12357739 C>G), RS1002979941 (8:7369273 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

4 total (human), top 4 by PubMed support.

ChemicalActions (top 5)PubMed papers
2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amideaffects cotreatment, decreases expression1
Benzo(a)pyrenedecreases methylation1
Caffeinedecreases phosphorylation1
Tetrachlorodibenzodioxindecreases expression, increases expression, affects cotreatment1

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.