ZNF705G
gene geneOn this page
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:37134 |
| Approved symbol | ZNF705G |
| Name | zinc finger protein 705G |
| Location | 8p23.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000215372 |
| Ensembl biotype | protein_coding |
| Entrez | 100131980 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00001621164 | 7381452 | 7381601 |
| ENSE00001647348 | 7359619 | 7359701 |
| ENSE00001663100 | 7361110 | 7361236 |
| ENSE00001681972 | 7385498 | 7385558 |
| ENSE00001774873 | 7360237 | 7360332 |
| ENSE00001793543 | 7362935 | 7363017 |
| ENSE00002171194 | 7355517 | 7358560 |
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):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sural nerve | UBERON:0015488 | 40.27 | gold quality |
| right testis | UBERON:0004534 | 37.57 | gold quality |
| ganglionic eminence | UBERON:0004023 | 37.22 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| left testis | UBERON:0004533 | 35.78 | gold quality |
| testis | UBERON:0000473 | 35.70 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 34.95 | gold quality |
| muscle tissue | UBERON:0002385 | 33.31 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| monocyte | CL:0000576 | 32.13 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| mucosa of stomach | UBERON:0001199 | 31.73 | gold quality |
| leukocyte | CL:0000738 | 31.72 | gold quality |
| prefrontal cortex | UBERON:0000451 | 30.27 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| right uterine tube | UBERON:0001302 | 29.21 | gold quality |
| tonsil | UBERON:0002372 | 28.60 | gold quality |
| liver | UBERON:0002107 | 28.29 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| urinary bladder | UBERON:0001255 | 27.59 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| primary visual cortex | UBERON:0002436 | 27.42 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 27.38 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 27.32 | gold quality |
| blood | UBERON:0000178 | 27.07 | gold quality |
| corpus callosum | UBERON:0002336 | 27.06 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.55 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.63 |
Regulation
Is transcription factor: no
Cross-species orthologs
5 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Zfp78 | ENSMUSG00000055150 |
| rattus_norvegicus | ENSRNOG00000083797 | |
| drosophila_melanogaster | CG2712 | FBGN0024975 |
| drosophila_melanogaster | Phs | FBGN0036522 |
| drosophila_melanogaster | CG3281 | FBGN0260741 |
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 705G — A8MUZ8 (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)
| 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 (6 total): zinc finger region 4, chain 1, domain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A8MUZ8-F1 | 67.40 | 0.15 |
Function
Pathways and Gene Ontology
Reactome pathways
1 pathways
| ID | Pathway |
|---|---|
| R-HSA-212436 | Generic 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:
| Category | Pathways |
|---|---|
| RNA Polymerase II Transcription | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| regulation of DNA-templated transcription | 1 |
| transcription by RNA polymerase II | 1 |
| DNA-templated transcription | 1 |
| regulation of gene expression | 1 |
| regulation of RNA biosynthetic process | 1 |
| transcription cis-regulatory region binding | 1 |
| chromatin | 1 |
| RNA polymerase II transcription regulatory region sequence-specific DNA binding | 1 |
| DNA-binding transcription factor activity | 1 |
| regulation of transcription by RNA polymerase II | 1 |
| transition metal ion binding | 1 |
| nucleic acid binding | 1 |
| cation binding | 1 |
| intracellular membrane-bounded organelle | 1 |
Protein interactions and networks
STRING
84 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| ZNF705G | SPATA31A6 | Q5VVP1 | 599 |
| ZNF705G | ANKRD20A4P | Q4UJ75 | 581 |
| ZNF705G | ENPP7 | Q6UWV6 | 541 |
| ZNF705G | BET1L | Q9NYM9 | 380 |
| ZNF705G | DNAJC8 | O75937 | 377 |
| ZNF705G | LRRC37A3 | O60309 | 374 |
| ZNF705G | EME2 | A4GXA9 | 367 |
| ZNF705G | WDR3 | Q9UNX4 | 348 |
| ZNF705G | CETN1 | Q12798 | 269 |
| ZNF705G | SF3B3 | Q15393 | 245 |
| ZNF705G | CETN2 | P41208 | 212 |
| ZNF705G | IARS1 | P41252 | 211 |
| ZNF705G | TNKS | O95271 | 203 |
| ZNF705G | HLA-DQA2 | P01906 | 160 |
| ZNF705G | HLA-DQB1 | P01917 | 145 |
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):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 82 |
| Likely benign | 7 |
| Benign | 1 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
981 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 8:7359612:AACTT:A | donor_loss | 1.0000 |
| 8:7359613:ACTTA:A | donor_loss | 1.0000 |
| 8:7359614:CTTAC:C | donor_loss | 1.0000 |
| 8:7359615:TTACC:T | donor_loss | 1.0000 |
| 8:7359616:TAC:T | donor_loss | 1.0000 |
| 8:7359617:A:AC | donor_gain | 1.0000 |
| 8:7359618:C:CC | donor_gain | 1.0000 |
| 8:7359698:CTGT:C | acceptor_gain | 1.0000 |
| 8:7359699:TGTC:T | acceptor_loss | 1.0000 |
| 8:7359711:T:TC | acceptor_gain | 1.0000 |
| 8:7360235:A:AC | donor_gain | 1.0000 |
| 8:7360236:C:CC | donor_gain | 1.0000 |
| 8:7361103:GACTC:G | donor_loss | 1.0000 |
| 8:7361104:ACTCA:A | donor_loss | 1.0000 |
| 8:7361105:CTCAC:C | donor_loss | 1.0000 |
| 8:7361106:TCA:T | donor_loss | 1.0000 |
| 8:7361107:CACCG:C | donor_loss | 1.0000 |
| 8:7361108:A:AC | donor_gain | 1.0000 |
| 8:7361108:ACCGA:A | donor_loss | 1.0000 |
| 8:7361109:C:CA | donor_gain | 1.0000 |
| 8:7361232:TTCTT:T | acceptor_gain | 1.0000 |
| 8:7361234:CTT:C | acceptor_gain | 1.0000 |
| 8:7361237:C:CC | acceptor_gain | 1.0000 |
| 8:7359617:AC:A | donor_gain | 0.9900 |
| 8:7359618:CC:C | donor_gain | 0.9900 |
| 8:7359618:CCA:C | donor_gain | 0.9900 |
| 8:7359699:TGT:T | acceptor_gain | 0.9900 |
| 8:7359700:GT:G | acceptor_gain | 0.9900 |
| 8:7359702:C:CC | acceptor_gain | 0.9900 |
| 8:7359711:T:C | acceptor_gain | 0.9900 |
AlphaMissense
2010 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 8:7358252:G:C | F209L | 0.977 |
| 8:7358252:G:T | F209L | 0.977 |
| 8:7358254:A:G | F209L | 0.977 |
| 8:7361121:A:G | L43P | 0.964 |
| 8:7361202:A:G | F16S | 0.964 |
| 8:7358000:G:C | F293L | 0.954 |
| 8:7358000:G:T | F293L | 0.954 |
| 8:7358002:A:G | F293L | 0.954 |
| 8:7361201:G:C | F16L | 0.954 |
| 8:7361201:G:T | F16L | 0.954 |
| 8:7361203:A:G | F16L | 0.954 |
| 8:7361155:A:C | Y32D | 0.945 |
| 8:7361188:A:G | W21R | 0.945 |
| 8:7361188:A:T | W21R | 0.945 |
| 8:7361139:A:G | L37P | 0.944 |
| 8:7361186:C:A | W21C | 0.943 |
| 8:7361186:C:G | W21C | 0.943 |
| 8:7361212:C:G | A13P | 0.941 |
| 8:7361222:A:C | F9L | 0.932 |
| 8:7361222:A:T | F9L | 0.932 |
| 8:7361224:A:G | F9L | 0.932 |
| 8:7358168:A:C | F237L | 0.924 |
| 8:7358168:A:T | F237L | 0.924 |
| 8:7358170:A:G | F237L | 0.924 |
| 8:7361162:T:A | R29S | 0.914 |
| 8:7361162:T:G | R29S | 0.914 |
| 8:7358313:C:G | R189P | 0.907 |
| 8:7361142:A:G | M36T | 0.904 |
| 8:7361136:T:A | E38V | 0.902 |
| 8:7361132:A:C | N39K | 0.886 |
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.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| 2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amide | affects cotreatment, decreases expression | 1 |
| Benzo(a)pyrene | decreases methylation | 1 |
| Caffeine | decreases phosphorylation | 1 |
| Tetrachlorodibenzodioxin | decreases expression, increases expression, affects cotreatment | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.