ZNF723
gene geneOn this page
Summary
ZNF723 (zinc finger protein 723, HGNC:32286) is a protein-coding gene on chromosome 19p12, encoding Zinc finger protein 723 (P0DPD5). 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 DNA-templated transcription. Predicted to be located in nucleus.
Source: NCBI Gene 646864 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001349726
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:32286 |
| Approved symbol | ZNF723 |
| Name | zinc finger protein 723 |
| Location | 19p12 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000268696 |
| Ensembl biotype | protein_coding |
| Entrez | 646864 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000600766
RefSeq mRNA: 1 — MANE Select: NM_001349726
NM_001349726
CCDS: CCDS86735
Canonical transcript exons
ENST00000600766 — 4 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001673752 | 22857118 | 22858667 |
| ENSE00002993203 | 22849198 | 22849293 |
| ENSE00003084768 | 22848261 | 22848387 |
| ENSE00003121959 | 22832291 | 22832382 |
Expression profiles
Bgee: expression breadth broad, 23 present calls, max score 77.26.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.1286 / max 52.8953, expressed in 22 samples.
FANTOM5 promoters (2 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 174906 | 0.0882 | 18 |
| 174907 | 0.0404 | 10 |
Top tissues by expression
107 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 77.26 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 77.08 | gold quality |
| testis | UBERON:0000473 | 56.20 | gold quality |
| right testis | UBERON:0004534 | 54.61 | gold quality |
| left testis | UBERON:0004533 | 54.59 | gold quality |
| sural nerve | UBERON:0015488 | 48.62 | silver quality |
| granulocyte | CL:0000094 | 43.88 | silver quality |
| ganglionic eminence | UBERON:0004023 | 43.08 | silver quality |
| placenta | UBERON:0001987 | 41.90 | gold quality |
| cortical plate | UBERON:0005343 | 40.79 | silver quality |
| endometrium | UBERON:0001295 | 39.20 | gold quality |
| bone marrow | UBERON:0002371 | 38.82 | gold quality |
| bone marrow cell | CL:0002092 | 38.71 | gold quality |
| stromal cell of endometrium | CL:0002255 | 38.49 | gold quality |
| islet of Langerhans | UBERON:0000006 | 37.88 | gold quality |
| duodenum | UBERON:0002114 | 37.21 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| muscle tissue | UBERON:0002385 | 36.28 | silver quality |
| pancreas | UBERON:0001264 | 36.14 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 36.08 | gold quality |
| monocyte | CL:0000576 | 35.86 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 35.59 | gold quality |
| vermiform appendix | UBERON:0001154 | 35.25 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 34.90 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 34.81 | gold quality |
| adrenal tissue | UBERON:0018303 | 34.79 | silver quality |
| tonsil | UBERON:0002372 | 34.44 | gold quality |
| urinary bladder | UBERON:0001255 | 33.86 | silver quality |
| left adrenal gland cortex | UBERON:0035825 | 33.15 | silver quality |
| adrenal gland | UBERON:0002369 | 32.60 | silver quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 3.13 |
| E-GEOD-99795 | no | 0.83 |
Regulation
Is transcription factor: no
Cross-species orthologs
1 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | ENSDARG00000099025 |
Paralogs (18): ZNF430 (ENSG00000118620), ZNF92 (ENSG00000146757), ZNF66 (ENSG00000160229), ZNF22 (ENSG00000165512), ZNF680 (ENSG00000173041), ZNF114 (ENSG00000178150), ZFP41 (ENSG00000181638), ZNF730 (ENSG00000183850), ZNF479 (ENSG00000185177), ZNF626 (ENSG00000188171), ZNF431 (ENSG00000196705), ZNF100 (ENSG00000197020), ZNF257 (ENSG00000197134), ZNF98 (ENSG00000197360), ZNF675 (ENSG00000197372), ZNF273 (ENSG00000198039), ZNF737 (ENSG00000237440), ZNF253 (ENSG00000256771)
Protein
Protein identifiers
Zinc finger protein 723 — P0DPD5 (reviewed: P0DPD5)
All UniProt accessions (1): P0DPD5
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_001336655* (*=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, PF13465
UniProt features (14 total): zinc finger region 12, chain 1, domain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0DPD5-F1 | 74.20 | 0.32 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 7 (showing top):
chr19p12, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, DESCARTES_FETAL_PLACENTA_SYNCYTIOTROPHOBLASTS_AND_VILLOUS_CYTOTROPHOBLASTS, GOMF_DNA_BINDING_TRANSCRIPTION_FACTOR_ACTIVITY, GOMF_CIS_REGULATORY_REGION_SEQUENCE_SPECIFIC_DNA_BINDING, GOMF_RNA_POLYMERASE_II_TRANSCRIPTION_REGULATORY_REGION_SEQUENCE_SPECIFIC_DNA_BINDING
GO Biological Process (2): regulation of DNA-templated transcription (GO:0006355), regulation of transcription by RNA polymerase II (GO:0006357)
GO Molecular Function (5): RNA polymerase II cis-regulatory region sequence-specific DNA binding (GO:0000978), 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)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| RNA polymerase II transcription regulatory region sequence-specific DNA binding | 2 |
| DNA-templated transcription | 1 |
| regulation of gene expression | 1 |
| regulation of RNA biosynthetic process | 1 |
| regulation of DNA-templated transcription | 1 |
| transcription by RNA polymerase II | 1 |
| cis-regulatory region sequence-specific DNA binding | 1 |
| chromatin | 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
60 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| ZNF723 | TMEM178B | H3BS89 | 608 |
| ZNF723 | ADGRF2P | Q8IZF7 | 571 |
| ZNF723 | LYPD1 | Q8N2G4 | 431 |
| ZNF723 | FXYD2 | P54710 | 397 |
| ZNF723 | SLFN11 | Q7Z7L1 | 375 |
| ZNF723 | ARNT2 | Q9HBZ2 | 363 |
| ZNF723 | RELN | P78509 | 271 |
| ZNF723 | LIPC | P11150 | 270 |
| ZNF723 | PLCG2 | P16885 | 224 |
| ZNF723 | AXIN2 | Q9Y2T1 | 193 |
| ZNF723 | MAPK1 | P28482 | 172 |
| ZNF723 | MST1R | Q04912 | 134 |
| ZNF723 | MVK | Q03426 | 64 |
| ZNF723 | NME8 | Q8N427 | 62 |
| ZNF723 | MED14 | O60244 | 57 |
| ZNF723 | JUN | P05412 | 57 |
IntAct
2 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| ZNF723 | ECE1 | psi-mi:“MI:0915”(physical association) | 0.370 |
ESM2 similar proteins: A6NK75, A6NNF4, A6NP11, A8MTY0, A8MUV8, B4DXR9, C9JN71, O75346, O75373, O95780, P0CJ79, P0DKX0, P0DPD5, P17019, P17035, P35789, Q03923, Q03938, Q08AN1, Q14593, Q15928, Q3SXZ3, Q3ZCX4, Q5MCW4, Q5R9S5, Q5RER9, Q68DY1, Q6JLC9, Q6ZMV8, Q6ZN06, Q6ZN08, Q6ZNA1, Q76KX8, Q86T29, Q86V71, Q8IYN0, Q8N4W9, Q8N7M2, Q8NEM1, Q8TD23
Diamond homologs: A0A1W2PQL4, A6NK75, A6NN14, A6NNF4, A6NP11, A8MQ14, A8MTY0, A8MUV8, A8MXY4, B4DX44, B4DXR9, E9PYI1, O14628, O43345, O75290, O75346, O75373, O75437, O95780, P0CB33, P0DKX0, P0DPD5, P16373, P17019, P17038, P21506, P35789, P52736, P52738, P52744, Q03923, Q03924, Q03936, Q03938, Q05481, Q14586, Q14593, Q14929, Q15928, Q3KNS6
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
3441 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 19:22858107:T:C | F406L | 0.987 |
| 19:22858109:T:A | F406L | 0.987 |
| 19:22858109:T:G | F406L | 0.987 |
| 19:22858191:T:C | F434L | 0.987 |
| 19:22858193:T:A | F434L | 0.987 |
| 19:22858193:T:G | F434L | 0.987 |
| 19:22857603:T:C | F238L | 0.979 |
| 19:22857605:T:A | F238L | 0.979 |
| 19:22857605:T:G | F238L | 0.979 |
| 19:22857855:T:C | F322L | 0.979 |
| 19:22857857:T:A | F322L | 0.979 |
| 19:22857857:T:G | F322L | 0.979 |
| 19:22857771:T:C | F294L | 0.977 |
| 19:22857773:T:A | F294L | 0.977 |
| 19:22857773:T:G | F294L | 0.977 |
| 19:22857687:T:C | F266L | 0.974 |
| 19:22857689:T:A | F266L | 0.974 |
| 19:22857689:T:G | F266L | 0.974 |
| 19:22858023:T:C | F378L | 0.974 |
| 19:22858025:T:A | F378L | 0.974 |
| 19:22858025:T:G | F378L | 0.974 |
| 19:22858275:T:C | F462L | 0.974 |
| 19:22858277:T:A | F462L | 0.974 |
| 19:22858277:T:G | F462L | 0.974 |
| 19:22857939:T:C | F350L | 0.956 |
| 19:22857941:C:A | F350L | 0.956 |
| 19:22857941:C:G | F350L | 0.956 |
| 19:22858126:T:C | L412P | 0.946 |
| 19:22858359:T:C | F490L | 0.945 |
| 19:22858361:T:A | F490L | 0.945 |
dbSNP variants (sampled 300 via entrez): RS1000052728 (19:22835278 G>C), RS1000058749 (19:22817246 T>C), RS1000103258 (19:22835454 A>G), RS1000111501 (19:22853178 T>C), RS1000163658 (19:22853451 C>T), RS1000170077 (19:22848223 T>C), RS1000330877 (19:22812363 C>T), RS1000401654 (19:22854956 A>C), RS1000498008 (19:22846888 G>A), RS1000500219 (19:22854845 C>G,T), RS1000630664 (19:22811939 G>A,T), RS1000663218 (19:22813665 C>T), RS1000745310 (19:22813163 G>A), RS1000751627 (19:22854657 A>G), RS1001059631 (19:22840458 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)
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.