ZNF735
gene geneOn this page
Summary
ZNF735 (zinc finger protein 735, HGNC:32466) is a protein-coding gene on chromosome 7q11.21, encoding Zinc finger protein 735 (P0CB33). May be involved in transcriptional regulation.
This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and nine C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation.
Source: NCBI Gene 730291 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 70 total
- MANE Select transcript:
NM_001159524
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:32466 |
| Approved symbol | ZNF735 |
| Name | zinc finger protein 735 |
| Location | 7q11.21 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000223614 |
| Ensembl biotype | protein_coding |
| Entrez | 730291 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000429565
RefSeq mRNA: 1 — MANE Select: NM_001159524
NM_001159524
CCDS: CCDS78236
Canonical transcript exons
ENST00000429565 — 4 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001714193 | 64219314 | 64220290 |
| ENSE00002467305 | 64214013 | 64214108 |
| ENSE00002519157 | 64213092 | 64213218 |
| ENSE00003758512 | 64207203 | 64207241 |
Expression profiles
Bgee: expression breadth not_expressed, 0 present calls, max score 37.20.
Top tissues by expression
127 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 33.38 | gold quality |
| muscle tissue | UBERON:0002385 | 32.15 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| sural nerve | UBERON:0015488 | 30.93 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| prefrontal cortex | UBERON:0000451 | 29.04 | gold quality |
| monocyte | CL:0000576 | 28.26 | gold quality |
| leukocyte | CL:0000738 | 28.20 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| liver | UBERON:0002107 | 28.04 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 26.91 | gold quality |
| urinary bladder | UBERON:0001255 | 26.74 | gold quality |
| blood | UBERON:0000178 | 26.58 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.55 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| gall bladder | UBERON:0002110 | 25.98 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 25.89 | gold quality |
| placenta | UBERON:0001987 | 25.81 | gold quality |
| muscle of leg | UBERON:0001383 | 25.04 | gold quality |
| primary visual cortex | UBERON:0002436 | 24.61 | gold quality |
| frontal cortex | UBERON:0001870 | 24.57 | gold quality |
| pancreas | UBERON:0001264 | 24.34 | gold quality |
| endometrium | UBERON:0001295 | 23.91 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 3.12 |
Regulation
Is transcription factor: no
Cross-species orthologs
0 orthologs
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 735 — P0CB33 (reviewed: P0CB33)
All UniProt accessions (1): P0CB33
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_001152996* (*=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 |
| IPR050589 | Ikaros_C2H2-ZF | Family |
Pfam: PF00096, PF01352
UniProt features (11 total): zinc finger region 9, chain 1, domain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0CB33-F1 | 68.42 | 0.16 |
Function
Pathways and Gene Ontology
Reactome pathways
1 pathways
| ID | Pathway |
|---|---|
| R-HSA-212436 | Generic Transcription Pathway |
MSigDB gene sets: 7 (showing top):
chr7q11, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, 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, REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION
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)
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 |
|---|---|
| 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
102 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| ZNF735 | SEC14L6 | B5MCN3 | 480 |
| ZNF735 | OR52E4 | Q8NGH9 | 469 |
| ZNF735 | BPY2 | O14599 | 447 |
| ZNF735 | USP17L1 | Q7RTZ2 | 393 |
| ZNF735 | TRIM60 | Q495X7 | 375 |
| ZNF735 | SPIDR | Q14159 | 337 |
| ZNF735 | SEC14L4 | Q9UDX3 | 310 |
| ZNF735 | HGSNAT | Q68CP4 | 305 |
| ZNF735 | RBMY1D | P0C7P1 | 305 |
| ZNF735 | FNTA | P49354 | 299 |
| ZNF735 | VCY | O14598 | 273 |
| ZNF735 | POMK | Q9H5K3 | 273 |
| ZNF735 | DAZ2 | Q13117 | 273 |
| ZNF735 | HOOK3 | Q86VS8 | 263 |
| ZNF735 | MAP1S | Q66K74 | 234 |
IntAct
2 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| ZNF735 | ECE1 | psi-mi:“MI:0915”(physical association) | 0.370 |
BioGRID (1): ZNF735 (Affinity Capture-MS)
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, 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
70 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 60 |
| Likely benign | 7 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
495 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 7:64207239:ATG:A | donor_gain | 1.0000 |
| 7:64207239:ATGGT:A | donor_loss | 1.0000 |
| 7:64207240:TG:T | donor_gain | 1.0000 |
| 7:64207240:TGGTG:T | donor_loss | 1.0000 |
| 7:64207241:GG:G | donor_gain | 1.0000 |
| 7:64207242:G:GG | donor_gain | 1.0000 |
| 7:64207242:GTG:G | donor_loss | 1.0000 |
| 7:64219312:A:AG | acceptor_gain | 1.0000 |
| 7:64219313:G:GA | acceptor_gain | 1.0000 |
| 7:64219313:GTTAC:G | acceptor_gain | 1.0000 |
| 7:64207238:AATG:A | donor_gain | 0.9900 |
| 7:64213086:TTTCA:T | acceptor_loss | 0.9900 |
| 7:64213087:TTCA:T | acceptor_loss | 0.9900 |
| 7:64213088:TCA:T | acceptor_loss | 0.9900 |
| 7:64213090:A:AC | acceptor_loss | 0.9900 |
| 7:64213090:A:AG | acceptor_gain | 0.9900 |
| 7:64213090:AG:A | acceptor_gain | 0.9900 |
| 7:64213090:AGG:A | acceptor_gain | 0.9900 |
| 7:64213091:G:GG | acceptor_gain | 0.9900 |
| 7:64213091:GG:G | acceptor_gain | 0.9900 |
| 7:64213091:GGG:G | acceptor_gain | 0.9900 |
| 7:64213091:GGGA:G | acceptor_gain | 0.9900 |
| 7:64213091:GGGAC:G | acceptor_gain | 0.9900 |
| 7:64213217:GG:G | donor_gain | 0.9900 |
| 7:64213218:GG:G | donor_gain | 0.9900 |
| 7:64213218:GGTGA:G | donor_loss | 0.9900 |
| 7:64213219:G:GG | donor_gain | 0.9900 |
| 7:64213219:GTGA:G | donor_loss | 0.9900 |
| 7:64213220:T:A | donor_loss | 0.9900 |
| 7:64219308:TTTCA:T | acceptor_loss | 0.9900 |
AlphaMissense
2739 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 7:64220219:T:C | F390L | 0.991 |
| 7:64220221:T:A | F390L | 0.991 |
| 7:64220221:T:G | F390L | 0.991 |
| 7:64220051:T:C | F334L | 0.989 |
| 7:64220053:T:A | F334L | 0.989 |
| 7:64220053:T:G | F334L | 0.989 |
| 7:64219883:T:C | F278L | 0.988 |
| 7:64219885:T:A | F278L | 0.988 |
| 7:64219885:T:G | F278L | 0.988 |
| 7:64219967:T:C | F306L | 0.988 |
| 7:64219969:T:A | F306L | 0.988 |
| 7:64219969:T:G | F306L | 0.988 |
| 7:64219799:T:C | F250L | 0.986 |
| 7:64219801:T:A | F250L | 0.986 |
| 7:64219801:T:G | F250L | 0.986 |
| 7:64220135:T:C | F362L | 0.970 |
| 7:64220137:T:A | F362L | 0.970 |
| 7:64220137:T:G | F362L | 0.970 |
| 7:64213125:T:C | F25L | 0.966 |
| 7:64213127:C:A | F25L | 0.966 |
| 7:64213127:C:G | F25L | 0.966 |
| 7:64219890:G:C | R280P | 0.965 |
| 7:64220176:T:A | H375Q | 0.951 |
| 7:64220176:T:G | H375Q | 0.951 |
| 7:64220220:T:C | F390S | 0.950 |
| 7:64213173:T:G | Y41D | 0.948 |
| 7:64220260:C:A | H403Q | 0.945 |
| 7:64220260:C:G | H403Q | 0.945 |
| 7:64220219:T:A | F390I | 0.938 |
| 7:64219968:T:C | F306S | 0.937 |
dbSNP variants (sampled 300 via entrez): RS1000205638 (7:64210446 G>A), RS1000306126 (7:64215421 T>C), RS1000306281 (7:64205211 C>A), RS1000707413 (7:64215139 GCAA>G), RS1000959565 (7:64220751 T>C), RS1002039598 (7:64210717 A>G), RS1002592562 (7:64211930 T>C), RS1002887866 (7:64216774 T>G), RS1003042823 (7:64211698 T>C), RS1003578659 (7:64207932 A>G), RS1003927065 (7:64207484 T>G), RS1004398808 (7:64212206 A>C,G), RS1004736973 (7:64217346 G>C), RS1005327287 (7:64213635 C>G), RS1005329419 (7:64218614 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
2 total (human), top 2 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| sodium arsenite | decreases expression | 1 |
| Benzo(a)pyrene | decreases methylation | 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.