ZNF878
gene geneOn this page
Summary
ZNF878 (zinc finger protein 878, HGNC:37246) is a protein-coding gene on chromosome 19p13.2, encoding Zinc finger protein 878 (C9JN71). 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 729747 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 7 total
- MANE Select transcript:
NM_001080404
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:37246 |
| Approved symbol | ZNF878 |
| Name | zinc finger protein 878 |
| Location | 19p13.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000257446 |
| Ensembl biotype | protein_coding |
| Entrez | 729747 |
Gene structure
Transcript identifiers
Ensembl transcripts: 2 — 2 protein_coding
ENST00000547628, ENST00000929191
RefSeq mRNA: 1 — MANE Select: NM_001080404
NM_001080404
CCDS: CCDS45984
Canonical transcript exons
ENST00000547628 — 4 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002351857 | 12052799 | 12052961 |
| ENSE00003476818 | 12046368 | 12046428 |
| ENSE00003499367 | 12046634 | 12046760 |
| ENSE00003544954 | 12043805 | 12045209 |
Expression profiles
Bgee: expression breadth ubiquitous, 122 present calls, max score 75.80.
FANTOM5 (CAGE): breadth broad, TPM avg 1.5280 / max 58.7241, expressed in 479 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 179285 | 1.5280 | 479 |
Top tissues by expression
128 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 75.80 | gold quality |
| placenta | UBERON:0001987 | 60.10 | gold quality |
| endometrium | UBERON:0001295 | 57.58 | gold quality |
| metanephros cortex | UBERON:0010533 | 56.84 | gold quality |
| ventricular zone | UBERON:0003053 | 56.69 | gold quality |
| ganglionic eminence | UBERON:0004023 | 56.23 | gold quality |
| right ovary | UBERON:0002118 | 55.61 | gold quality |
| islet of Langerhans | UBERON:0000006 | 55.44 | gold quality |
| tonsil | UBERON:0002372 | 55.30 | gold quality |
| bone marrow | UBERON:0002371 | 55.23 | gold quality |
| right adrenal gland | UBERON:0001233 | 55.07 | gold quality |
| stromal cell of endometrium | CL:0002255 | 55.03 | silver quality |
| adult mammalian kidney | UBERON:0000082 | 54.93 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 54.61 | gold quality |
| pancreas | UBERON:0001264 | 54.58 | gold quality |
| body of pancreas | UBERON:0001150 | 54.52 | gold quality |
| cortex of kidney | UBERON:0001225 | 54.46 | gold quality |
| kidney | UBERON:0002113 | 54.44 | gold quality |
| left adrenal gland | UBERON:0001234 | 54.35 | gold quality |
| left ovary | UBERON:0002119 | 54.28 | gold quality |
| ovary | UBERON:0000992 | 53.84 | gold quality |
| myometrium | UBERON:0001296 | 53.04 | gold quality |
| cerebellar cortex | UBERON:0002129 | 52.80 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 52.78 | gold quality |
| cerebellum | UBERON:0002037 | 52.72 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 52.65 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 52.26 | gold quality |
| colonic epithelium | UBERON:0000397 | 52.19 | gold quality |
| adrenal gland | UBERON:0002369 | 52.17 | gold quality |
| lower esophagus | UBERON:0013473 | 52.12 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.26 |
Regulation
Is transcription factor: yes
JASPAR motifs
| Motif | Name | Family |
|---|---|---|
| MA2574.1 | ZNF878 | More than 3 adjacent zinc fingers |
JASPAR matrix evidence (PMIDs): PMID:39605320
Upstream regulators (CollecTRI, top): STAT1
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Zfp867 | ENSMUSG00000054519 |
| rattus_norvegicus | Zfp867 | ENSRNOG00000022431 |
Paralogs (15): ZNF14 (ENSG00000105708), ZNF57 (ENSG00000171970), ZNF791 (ENSG00000173875), ZNF443 (ENSG00000180855), ZNF101 (ENSG00000181896), ZNF563 (ENSG00000188868), ZNF799 (ENSG00000196466), ZNF700 (ENSG00000196757), ZNF441 (ENSG00000197044), ZNF433 (ENSG00000197647), ZNF44 (ENSG00000197857), ZNF823 (ENSG00000197933), ZNF442 (ENSG00000198342), ZNF844 (ENSG00000223547), ZNF709 (ENSG00000242852)
Protein
Protein identifiers
Zinc finger protein 878 — C9JN71 (reviewed: C9JN71)
All UniProt accessions (1): C9JN71
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_001073873* (*=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 (17 total): zinc finger region 15, chain 1, domain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-C9JN71-F1 | 78.93 | 0.44 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 27 (showing top):
FOSTER_TOLERANT_MACROPHAGE_DN, BYSTRYKH_HEMATOPOIESIS_STEM_CELL_AND_BRAIN_QTL_CIS, TSENG_IRS1_TARGETS_DN, ZHANG_BREAST_CANCER_PROGENITORS_UP, chr19p13, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, MIKKELSEN_ES_ICP_WITH_H3K4ME3, BAKKER_FOXO3_TARGETS_DN, TORCHIA_TARGETS_OF_EWSR1_FLI1_FUSION_DN, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, GSE7568_CTRL_VS_24H_TGFB_TREATED_MACROPHAGES_WITH_IL4_AND_DEXAMETHASONE_UP, MANNO_MIDBRAIN_NEUROTYPES_HPROGBP, MANNO_MIDBRAIN_NEUROTYPES_HNBM, MANNO_MIDBRAIN_NEUROTYPES_HNBML1, GOMF_DNA_BINDING_TRANSCRIPTION_FACTOR_ACTIVITY
GO Biological Process (2): regulation of transcription by RNA polymerase II (GO:0006357), regulation of DNA-templated transcription (GO:0006355)
GO Molecular Function (4): 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), 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 |
|---|---|
| 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 |
| cation binding | 1 |
| intracellular membrane-bounded organelle | 1 |
Protein interactions and networks
STRING
142 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| ZNF878 | C8orf48 | Q96LL4 | 578 |
| ZNF878 | FHIP2A | Q5W0V3 | 419 |
| ZNF878 | ZNF704 | Q6ZNC4 | 358 |
| ZNF878 | DNAAF3 | Q8N9W5 | 305 |
| ZNF878 | ADAP1 | O75689 | 304 |
| ZNF878 | DMRTA2 | Q96SC8 | 302 |
| ZNF878 | CREB3L4 | Q8TEY5 | 296 |
| ZNF878 | PAFAH1B3 | Q15102 | 276 |
| ZNF878 | ZNF451 | Q9Y4E5 | 272 |
| ZNF878 | IVD | P26440 | 272 |
| ZNF878 | CYTL1 | Q9NRR1 | 257 |
| ZNF878 | THOP1 | P52888 | 251 |
| ZNF878 | RABAC1 | Q9UI14 | 250 |
| ZNF878 | SAMSN1 | Q9NSI8 | 248 |
| ZNF878 | NIPA1 | Q7RTP0 | 243 |
IntAct
4 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| ZNF878 | H2BC9 | psi-mi:“MI:0915”(physical association) | 0.400 |
| ZNF878 | ECE1 | psi-mi:“MI:0915”(physical association) | 0.370 |
| INSR | RIMOC1 | psi-mi:“MI:0914”(association) | 0.350 |
BioGRID (6): HIST1H2BH (Proximity Label-MS), ZNF878 (Protein-peptide), ZNF878 (Affinity Capture-MS), KIF5B (Cross-Linking-MS (XL-MS)), ZNF878 (Proximity Label-MS), ZNF878 (Proximity Label-MS)
ESM2 similar proteins: A6NDX5, A6NK75, A6NNF4, A6NP11, B4DXR9, B7Z6K7, C9JN71, O43361, O75290, O75373, P0CJ79, P0DKX0, P17019, P17021, P17035, P17039, P35789, Q02386, Q03938, Q08AN1, Q13106, Q15928, Q3ZCX4, Q5R9F0, Q5SXM1, Q68EA5, Q6P9A1, Q6PDB4, Q6ZN06, Q6ZN08, Q6ZNG1, Q76KX8, Q86V71, Q86XN6, Q8IYB9, Q8N4W9, Q8NEP9, Q8TBZ8, Q8TC21, Q8TF32
Diamond homologs: A0JPK3, A8MT65, C9JN71, E9QAG8, G3X9G7, O75820, P16373, P16374, P16415, P17017, P17024, P17025, P51815, P52737, Q08AG5, Q08ER8, Q0D2J5, Q15973, Q2M218, Q3KP31, Q3V080, Q494X3, Q4R4C7, Q5MYW4, Q5R9F0, Q5R9S5, Q5REI6, Q5REK1, Q68EA5, Q6P560, Q6P5C7, Q6ZQV5, Q7L945, Q86T29, Q8BGV5, Q8C6P8, Q8IYI8, Q8IZC7, Q8N7K0, Q8N972
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
7 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 7 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
666 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 19:12046628:TCTTA:T | donor_loss | 1.0000 |
| 19:12046629:CTTA:C | donor_loss | 1.0000 |
| 19:12046630:TTA:T | donor_loss | 1.0000 |
| 19:12046632:A:AC | donor_gain | 1.0000 |
| 19:12046633:C:CC | donor_gain | 1.0000 |
| 19:12046771:CCACA:C | acceptor_gain | 1.0000 |
| 19:12046772:CACA:C | acceptor_gain | 1.0000 |
| 19:12046775:A:C | acceptor_gain | 1.0000 |
| 19:12052794:CTCA:C | donor_loss | 1.0000 |
| 19:12052795:TCA:T | donor_loss | 1.0000 |
| 19:12052796:CACCA:C | donor_loss | 1.0000 |
| 19:12052798:C:CT | donor_loss | 1.0000 |
| 19:12045207:CTT:C | acceptor_gain | 0.9900 |
| 19:12045208:TT:T | acceptor_gain | 0.9900 |
| 19:12045210:C:CC | acceptor_gain | 0.9900 |
| 19:12046443:C:T | acceptor_gain | 0.9900 |
| 19:12046672:T:TA | donor_gain | 0.9900 |
| 19:12046673:C:A | donor_gain | 0.9900 |
| 19:12046759:TC:T | acceptor_gain | 0.9900 |
| 19:12046759:TCCTG:T | acceptor_loss | 0.9900 |
| 19:12046760:CC:C | acceptor_gain | 0.9900 |
| 19:12046760:CCTG:C | acceptor_loss | 0.9900 |
| 19:12046760:CCTGA:C | acceptor_loss | 0.9900 |
| 19:12046772:C:T | acceptor_gain | 0.9900 |
| 19:12046774:CA:C | acceptor_gain | 0.9900 |
| 19:12046775:A:AC | acceptor_gain | 0.9900 |
| 19:12052129:CA:C | donor_gain | 0.9900 |
| 19:12052797:A:AC | donor_gain | 0.9900 |
| 19:12052797:AC:A | donor_gain | 0.9900 |
| 19:12052798:C:CC | donor_gain | 0.9900 |
AlphaMissense
3538 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 19:12044357:G:C | F348L | 0.992 |
| 19:12044357:G:T | F348L | 0.992 |
| 19:12044359:A:G | F348L | 0.992 |
| 19:12043853:A:C | F516L | 0.986 |
| 19:12043853:A:T | F516L | 0.986 |
| 19:12043855:A:G | F516L | 0.986 |
| 19:12044189:G:C | F404L | 0.986 |
| 19:12044189:G:T | F404L | 0.986 |
| 19:12044191:A:G | F404L | 0.986 |
| 19:12043937:G:C | F488L | 0.984 |
| 19:12043937:G:T | F488L | 0.984 |
| 19:12043939:A:G | F488L | 0.984 |
| 19:12044021:G:C | F460L | 0.984 |
| 19:12044021:G:T | F460L | 0.984 |
| 19:12044023:A:G | F460L | 0.984 |
| 19:12044525:G:C | F292L | 0.983 |
| 19:12044525:G:T | F292L | 0.983 |
| 19:12044527:A:G | F292L | 0.983 |
| 19:12044162:G:C | H413Q | 0.982 |
| 19:12044162:G:T | H413Q | 0.982 |
| 19:12044105:A:C | F432L | 0.981 |
| 19:12044105:A:T | F432L | 0.981 |
| 19:12044107:A:G | F432L | 0.981 |
| 19:12044441:A:C | F320L | 0.981 |
| 19:12044441:A:T | F320L | 0.981 |
| 19:12044443:A:G | F320L | 0.981 |
| 19:12044269:A:G | S378P | 0.978 |
| 19:12044437:A:G | S322P | 0.977 |
| 19:12044861:G:C | F180L | 0.977 |
| 19:12044861:G:T | F180L | 0.977 |
dbSNP variants (sampled 300 via entrez): RS1000060186 (19:12047996 A>G), RS1000189957 (19:12047779 G>A), RS1000196831 (19:12051498 G>A), RS1000270526 (19:12051832 G>A), RS1000529517 (19:12050142 T>C), RS1000603150 (19:12050341 C>T), RS1000791658 (19:12043175 A>G), RS1000999203 (19:12052269 A>G), RS1001201470 (19:12052938 A>C,G), RS1001462058 (19:12046038 T>A), RS1001600155 (19:12047053 A>C,G), RS1001829695 (19:12045852 A>G), RS1001886312 (19:12045477 C>A,G,T), RS1002497854 (19:12051888 A>G), RS1002763096 (19:12050203 C>A,T)
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
7 total (human), top 7 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| methyleugenol | increases expression | 1 |
| 2-methyl-4-isothiazolin-3-one | increases expression | 1 |
| Benzo(a)pyrene | increases methylation | 1 |
| Oxygen | decreases expression | 1 |
| Smoke | decreases expression | 1 |
| Urethane | increases expression | 1 |
| Okadaic Acid | increases expression | 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.