ZNF488

gene
On this page

Also known as FLJ32104

Summary

ZNF488 (zinc finger protein 488, HGNC:23535) is a protein-coding gene on chromosome 10q11.22, encoding Zinc finger protein 488 (Q96MN9). Transcriptional repressor.

Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in oligodendrocyte development and regulation of DNA-templated transcription. Predicted to act upstream of or within negative regulation of DNA-templated transcription and positive regulation of oligodendrocyte differentiation. Predicted to be active in nucleus.

Source: NCBI Gene 118738 — RefSeq curated summary.

At a glance

  • GWAS associations: 4
  • Clinical variants (ClinVar): 69 total
  • MANE Select transcript: NM_153034

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:23535
Approved symbolZNF488
Namezinc finger protein 488
Location10q11.22
Locus typegene with protein product
StatusApproved
AliasesFLJ32104
Ensembl geneENSG00000265763
Ensembl biotypeprotein_coding
Entrez118738

Gene structure

Transcript identifiers

Ensembl transcripts: 12 — 12 protein_coding

ENST00000585316, ENST00000591025, ENST00000884605, ENST00000884606, ENST00000884607, ENST00000884608, ENST00000884609, ENST00000884610, ENST00000884611, ENST00000884612, ENST00000884613, ENST00000919271

RefSeq mRNA: 6 — MANE Select: NM_153034 NM_001346932, NM_001346933, NM_001346934, NM_001346935, NM_001346936, NM_153034

CCDS: CCDS73120

Canonical transcript exons

ENST00000585316 — 2 exons

ExonStartEnd
ENSE000026925824736549647368937
ENSE000027150474738422047384293

Expression profiles

Bgee: expression breadth ubiquitous, 142 present calls, max score 94.12.

FANTOM5 (CAGE): breadth broad, TPM avg 4.9399 / max 508.2662, expressed in 620 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1092824.9399620

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
C1 segment of cervical spinal cordUBERON:000646994.12gold quality
spinal cordUBERON:000224093.47gold quality
ileal mucosaUBERON:000033190.06gold quality
inferior vagus X ganglionUBERON:000536389.63gold quality
substantia nigraUBERON:000203885.25gold quality
midbrainUBERON:000189184.63gold quality
jejunal mucosaUBERON:000039984.52gold quality
Ammon’s hornUBERON:000195483.10gold quality
duodenumUBERON:000211482.96gold quality
prefrontal cortexUBERON:000045181.79gold quality
medulla oblongataUBERON:000189681.55gold quality
subthalamic nucleusUBERON:000190681.14gold quality
ponsUBERON:000098880.57gold quality
Brodmann (1909) area 9UBERON:001354079.58gold quality
corpus callosumUBERON:000233679.21gold quality
frontal cortexUBERON:000187078.35gold quality
putamenUBERON:000187478.22gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047378.14gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099178.10gold quality
right frontal lobeUBERON:000281078.09gold quality
dorsolateral prefrontal cortexUBERON:000983477.42gold quality
cerebral cortexUBERON:000095677.33gold quality
neocortexUBERON:000195077.11gold quality
superior vestibular nucleusUBERON:000722777.01gold quality
hypothalamusUBERON:000189876.84gold quality
caudate nucleusUBERON:000187376.66gold quality
substantia nigra pars reticulataUBERON:000196676.63silver quality
Brodmann (1909) area 46UBERON:000648376.34gold quality
ventral tegmental areaUBERON:000269176.28gold quality
amygdalaUBERON:000187676.26gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.22

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

74 targeting ZNF488, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-6867-5P100.0082.213464
HSA-MIR-1252-5P100.0069.802774
HSA-MIR-3692-3P99.9870.272139
HSA-MIR-60799.9773.625593
HSA-MIR-9-3P99.9670.882068
HSA-MIR-568099.9169.833421
HSA-MIR-4731-5P99.8967.232537
HSA-MIR-449299.8768.253611
HSA-MIR-63699.8069.581500
HSA-MIR-182599.7268.111089
HSA-MIR-10393-3P99.7266.56961
HSA-MIR-6801-5P99.7266.50981
HSA-MIR-7154-5P99.6970.521900
HSA-MIR-366099.6867.331149
HSA-MIR-452699.6867.071136
HSA-MIR-6762-3P99.6666.941188
HSA-MIR-120599.6566.761826
HSA-MIR-182799.6368.573265
HSA-MIR-6757-3P99.6366.881089
HSA-MIR-613499.6365.681537
HSA-MIR-1249-5P99.6166.552049
HSA-MIR-426199.5970.303415
HSA-MIR-205399.5769.151635
HSA-MIR-444199.4966.563216
HSA-MIR-6727-3P99.4965.921333
HSA-MIR-608199.4866.071446
HSA-MIR-94099.3766.142064
HSA-MIR-4722-3P99.3565.221099
HSA-MIR-501-3P99.3366.12651
HSA-MIR-502-3P99.3366.12651

Literature-anchored findings (GeneRIF, showing 1)

  • Transcription factor ZNF488 accelerates cervical cancer progression through regulating the MEK/ERK signaling pathway. (PMID:36537752)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_rerioznf488ENSDARG00000025017
mus_musculusZfp488ENSMUSG00000044519
rattus_norvegicusZfp488ENSRNOG00000057542
drosophila_melanogasterCG13287FBGN0035643

Paralogs (1): PRDM8 (ENSG00000152784)

Protein

Protein identifiers

Zinc finger protein 488Q96MN9 (reviewed: Q96MN9)

All UniProt accessions (1): Q96MN9

UniProt curated annotations — full annotation on UniProt →

Function. Transcriptional repressor. Plays a role in oligodendrocyte differentiation, together with OLIG2. Mediates Notch signaling-activated formation of oligodendrocyte precursors. Promotes differentiation of adult neural stem progenitor cells (NSPCs) into mature oligodendrocytes and contributes to remyelination following nerve injury.

Subunit / interactions. Interacts with OLIG2.

Subcellular location. Nucleus.

Similarity. Belongs to the krueppel C2H2-type zinc-finger protein family.

Isoforms (2)

UniProt IDNamesCanonical?
Q96MN9-11yes
Q96MN9-22

RefSeq proteins (6): NP_001333861, NP_001333862, NP_001333863, NP_001333864, NP_001333865, NP_694579* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR013087Znf_C2H2_typeDomain
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR052296TR-Histone_MethyltransFamily

UniProt features (12 total): sequence variant 3, zinc finger region 2, region of interest 2, compositionally biased region 2, chain 1, short sequence motif 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96MN9-F156.630.14

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 64 (showing top): GSE45365_NK_CELL_VS_CD8A_DC_MCMV_INFECTION_UP, GSE37336_LY6C_POS_VS_NEG_NAIVE_CD4_TCELL_DN, GOBP_POSITIVE_REGULATION_OF_GLIAL_CELL_DIFFERENTIATION, GOBP_GLIAL_CELL_DEVELOPMENT, GOBP_NEUROGENESIS, GOBP_REGULATION_OF_MYELINATION, GOBP_REGULATION_OF_NERVOUS_SYSTEM_DEVELOPMENT, GOBP_POSITIVE_REGULATION_OF_NERVOUS_SYSTEM_DEVELOPMENT, GOBP_POSITIVE_REGULATION_OF_OLIGODENDROCYTE_DIFFERENTIATION, GOBP_POSITIVE_REGULATION_OF_CELL_DIFFERENTIATION, GOBP_ENSHEATHMENT_OF_NEURONS, GOBP_REGULATION_OF_OLIGODENDROCYTE_DIFFERENTIATION, GOBP_POSITIVE_REGULATION_OF_NERVOUS_SYSTEM_PROCESS, GOBP_REGULATION_OF_NERVOUS_SYSTEM_PROCESS, GOBP_REGULATION_OF_SYSTEM_PROCESS

GO Biological Process (6): regulation of DNA-templated transcription (GO:0006355), oligodendrocyte development (GO:0014003), positive regulation of myelination (GO:0031643), negative regulation of DNA-templated transcription (GO:0045892), positive regulation of oligodendrocyte differentiation (GO:0048714), nervous system development (GO:0007399)

GO Molecular Function (4): DNA binding (GO:0003677), zinc ion binding (GO:0008270), protein binding (GO:0005515), metal ion binding (GO:0046872)

GO Cellular Component (1): nucleus (GO:0005634)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
DNA-templated transcription2
oligodendrocyte differentiation2
regulation of gene expression1
regulation of RNA biosynthetic process1
glial cell development1
regulation of myelination1
positive regulation of nervous system process1
myelination1
positive regulation of cellular process1
regulation of DNA-templated transcription1
negative regulation of RNA biosynthetic process1
positive regulation of glial cell differentiation1
regulation of oligodendrocyte differentiation1
system development1
nucleic acid binding1
transition metal ion binding1
binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

622 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF488OLIG2Q13516572
ZNF488SNAPC3Q92966548
ZNF488ASXL1Q8IXJ9481
ZNF488ANTXRLA6NF34476
ZNF488WDR64B1ANS9418
ZNF488KMT2DO14686409
ZNF488ZNF487B1APH4377
ZNF488A0A1B0GU03A0A1B0GU03375
ZNF488AGAP6Q5VW22371
ZNF488OLIG1Q8TAK6354
ZNF488MAP7D2Q96T17348
ZNF488ASAH2BP0C7U1348
ZNF488GLTPD2A6NH11342
ZNF488DIPK1BQ5VUD6322
ZNF488UGT8Q16880321
ZNF488FAM25AB3EWG3321

IntAct

42 interactions, top by confidence:

ABTypeScore
ATXN1ZNF488psi-mi:“MI:0915”(physical association)0.780
GOLGA2ZNF488psi-mi:“MI:0915”(physical association)0.670
ZNF488RBPMSpsi-mi:“MI:0915”(physical association)0.670
ZNF488GOLGA2psi-mi:“MI:0915”(physical association)0.670
RBPMSZNF488psi-mi:“MI:0915”(physical association)0.670
DAB1ZNF488psi-mi:“MI:0915”(physical association)0.560
ZNF488PRR20Cpsi-mi:“MI:0915”(physical association)0.560
TRAF2ZNF488psi-mi:“MI:0915”(physical association)0.560
ZNF488KRT40psi-mi:“MI:0915”(physical association)0.560
BANPZNF488psi-mi:“MI:0915”(physical association)0.560
ZNF488RIMBP3psi-mi:“MI:0915”(physical association)0.560
MAGED1ZNF488psi-mi:“MI:0915”(physical association)0.560
PRR20CZNF488psi-mi:“MI:0915”(physical association)0.560
KRT40ZNF488psi-mi:“MI:0915”(physical association)0.560
ZNF488BANPpsi-mi:“MI:0915”(physical association)0.560
RIMBP3ZNF488psi-mi:“MI:0915”(physical association)0.560
ZNF488TRAF2psi-mi:“MI:0915”(physical association)0.560

BioGRID (25): ZNF488 (Two-hybrid), ZNF488 (Two-hybrid), ZNF488 (Two-hybrid), ZNF488 (Two-hybrid), ZNF488 (Two-hybrid), ZNF488 (Two-hybrid), ZNF488 (Two-hybrid), PRR20A (Two-hybrid), KRT40 (Two-hybrid), USO1 (Affinity Capture-MS), CTH (Affinity Capture-MS), GOPC (Affinity Capture-MS), HSPA8 (Affinity Capture-MS), CAMK2G (Affinity Capture-MS), ZNF488 (Two-hybrid)

ESM2 similar proteins: A0A5F9ZHS7, A1YGK1, A2T7E6, A8MZG2, O08574, O43593, O60393, O75593, O88621, O95231, P0C1T1, P0CG20, P20428, P97609, Q04667, Q17QR5, Q2KIS6, Q2M1V0, Q2T9Q7, Q32LE6, Q497V6, Q5JUK2, Q5M844, Q5RJB0, Q5TGS1, Q61645, Q61657, Q6ZMY3, Q6ZN32, Q6ZNG2, Q7RTU1, Q8BZW2, Q8CGW9, Q8IWN7, Q8IXT2, Q8IZ20, Q8N1L9, Q8N7G0, Q8N944, Q8N9Y4

Diamond homologs: A0A163UT06, A2AGX3, B8A5Y1, E9PZZ1, Q5HZG9, Q8BZ97, Q96MN9, Q9H4Q3, Q9NQV5, Q9NQV7, Q9NQV8, A2AJ77, E9Q3T6, P0C6Y7, Q96EQ9, Q9GZV8, Q9H4Q4, Q9NQW5

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance60
Likely benign9
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

610 predictions. Top by Δscore:

VariantEffectΔscore
10:47357098:T:Gacceptor_loss0.9900
10:47357099:C:CCacceptor_gain0.9900
10:47357099:CT:Cacceptor_loss0.9900
10:47357100:CCTGG:Cacceptor_loss0.9900
10:47357101:ACCTG:Aacceptor_loss0.9900
10:47357102:CAC:Cacceptor_gain0.9900
10:47384216:T:Gdonor_loss0.9900
10:47384217:G:Adonor_loss0.9900
10:47384219:AGG:Adonor_loss0.9900
10:47384220:CAGG:Cdonor_loss0.9900
10:47357102:CACC:Cacceptor_gain0.9800
10:47357103:TCAC:Tacceptor_gain0.9800
10:47384217:G:GGdonor_gain0.9800
10:47357104:TTCAC:Tacceptor_gain0.9700
10:47370661:T:Gdonor_gain0.9700
10:47357096:GAAGA:Gacceptor_loss0.9600
10:47357097:GGAAG:Gacceptor_loss0.9500
10:47357100:CC:Cacceptor_gain0.9500
10:47357101:AC:Aacceptor_gain0.9500
10:47368936:GG:Gacceptor_gain0.9000
10:47368937:AG:Aacceptor_gain0.9000
10:47380866:A:AGacceptor_gain0.9000
10:47368936:G:GAacceptor_loss0.8700
10:47368937:A:Tacceptor_loss0.8700
10:47368938:CA:Cacceptor_loss0.8700
10:47368939:GCA:Gacceptor_loss0.8700
10:47368940:TGCA:Tacceptor_loss0.8700
10:47368941:CTGCA:Cacceptor_loss0.8700
10:47380865:A:Gacceptor_gain0.8700
10:47356767:T:TAdonor_gain0.8600

AlphaMissense

2167 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
10:47367978:A:CF284L0.996
10:47367978:A:TF284L0.996
10:47367980:A:GF284L0.996
10:47367852:G:CF326L0.995
10:47367852:G:TF326L0.995
10:47367854:A:GF326L0.995
10:47367948:C:AM294I0.995
10:47367948:C:GM294I0.995
10:47367948:C:TM294I0.995
10:47367953:G:CH293D0.995
10:47367949:A:GM294T0.994
10:47367979:A:GF284S0.993
10:47367813:G:CH339Q0.992
10:47367813:G:TH339Q0.992
10:47367825:G:CH335Q0.992
10:47367825:G:TH335Q0.992
10:47367953:G:TH293N0.992
10:47367951:G:CH293Q0.991
10:47367951:G:TH293Q0.991
10:47368341:A:CF163L0.990
10:47368341:A:TF163L0.990
10:47368343:A:GF163L0.990
10:47367827:G:CH335D0.989
10:47367827:G:TH335N0.989
10:47367837:G:CH331Q0.989
10:47367837:G:TH331Q0.989
10:47367853:A:CF326C0.989
10:47367853:A:GF326S0.988
10:47367961:A:GL290P0.988
10:47367991:C:GC280S0.986

dbSNP variants (sampled 300 via entrez): RS1000011649 (10:47384820 C>G,T), RS1000205387 (10:47367803 C>A,T), RS1000253876 (10:47367543 C>T), RS1000351922 (10:47373293 C>T), RS1000902817 (10:47377610 A>T), RS1000960432 (10:47384316 C>A), RS1001012636 (10:47384025 C>G), RS1001362805 (10:47371941 C>G,T), RS1001372619 (10:47371673 C>T), RS1001613456 (10:47366507 G>A), RS1002308761 (10:47376285 C>G), RS1002375468 (10:47370124 C>T), RS1002479804 (10:47376558 C>T), RS1002964041 (10:47381016 A>T), RS1003372500 (10:47369110 C>A)

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

4 associations (top):

StudyTraitp-value
GCST005362_10Attention deficit hyperactivity disorder7.000000e-07
GCST005559_6Virologic severity in Herpes simplex virus type 2 infection3.000000e-06
GCST006976_33Macular thickness2.000000e-18
GCST010002_287Refractive error2.000000e-49

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0009010HSV2 virologic severity measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

34 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
bisphenol Aaffects expression, decreases expression, increases methylation2
sodium arsenitedecreases expression2
Benzo(a)pyrenedecreases methylation, increases expression, increases methylation, affects methylation2
Estradiolaffects cotreatment, decreases expression, increases expression2
ethyl-p-hydroxybenzoateincreases expression1
beta-lapachonedecreases expression1
tris(1,3-dichloro-2-propyl)phosphatedecreases expression1
manganese chlorideincreases abundance, increases expression1
perfluorooctane sulfonic aciddecreases expression1
pentabromodiphenyl etherdecreases expression1
pterostilbenedecreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, increases expression1
abrinedecreases expression1
2,2’,4,4’-tetrabromodiphenyl etherdecreases expression1
dorsomorphinaffects cotreatment, increases expression1
jinfukangaffects cotreatment, increases expression1
Resveratrolaffects cotreatment, decreases expression1
Troglitazonedecreases expression1
Air Pollutantsincreases abundance, decreases expression1
Calcitrioldecreases expression1
Cannabidioldecreases expression1
Cisplatinincreases expression, affects cotreatment1
Manganeseincreases abundance, increases expression1
Phenylmercuric Acetateaffects cotreatment, increases expression1
Plant Extractsaffects cotreatment, decreases expression1
Silicon Dioxideincreases expression1
Triclosanincreases expression1
Valproic Aciddecreases expression1
Aflatoxin B1increases expression1
Antirheumatic Agentsincreases expression1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_HD26HEK293 eGFP-ZNF488Transformed cell lineFemale

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.