ZNF585B

gene
On this page

Also known as FLJ14928SZFP41Zfp27

Summary

ZNF585B (zinc finger protein 585B, HGNC:30948) is a protein-coding gene on chromosome 19q13.12, encoding Zinc finger protein 585B (Q52M93). May be involved in transcriptional regulation.

Predicted to enable zinc ion binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.

Source: NCBI Gene 92285 — RefSeq curated summary.

At a glance

  • GWAS associations: 3
  • Clinical variants (ClinVar): 109 total
  • MANE Select transcript: NM_152279

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:30948
Approved symbolZNF585B
Namezinc finger protein 585B
Location19q13.12
Locus typegene with protein product
StatusApproved
AliasesFLJ14928, SZFP41, Zfp27
Ensembl geneENSG00000245680
Ensembl biotypeprotein_coding
Entrez92285

Gene structure

Transcript identifiers

Ensembl transcripts: 12 — 6 protein_coding, 4 nonsense_mediated_decay, 1 retained_intron, 1 protein_coding_CDS_not_defined

ENST00000392156, ENST00000526705, ENST00000527838, ENST00000531805, ENST00000532828, ENST00000534363, ENST00000586320, ENST00000591273, ENST00000591492, ENST00000905951, ENST00000905952, ENST00000965087

RefSeq mRNA: 1 — MANE Select: NM_152279 NM_152279

CCDS: CCDS12500

Canonical transcript exons

ENST00000532828 — 5 exons

ExonStartEnd
ENSE000021741283721044137210536
ENSE000029567453718157937187244
ENSE000034723363718966137189753
ENSE000035362433720704037207254
ENSE000035574763719002437190150

Expression profiles

Bgee: expression breadth ubiquitous, 219 present calls, max score 84.27.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 4.5750 / max 86.1217, expressed in 1438 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1807084.57501438

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
secondary oocyteCL:000065584.27gold quality
calcaneal tendonUBERON:000370183.51gold quality
colonic epitheliumUBERON:000039782.70gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099182.48gold quality
oocyteCL:000002381.05gold quality
islet of LangerhansUBERON:000000680.59gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047380.55gold quality
right lobe of thyroid glandUBERON:000111980.45gold quality
adrenal tissueUBERON:001830380.36gold quality
cerebellar hemisphereUBERON:000224580.25gold quality
cerebellar cortexUBERON:000212980.21gold quality
pituitary glandUBERON:000000780.12gold quality
thyroid glandUBERON:000204679.96gold quality
left lobe of thyroid glandUBERON:000112079.93gold quality
left ovaryUBERON:000211979.70gold quality
apex of heartUBERON:000209879.65gold quality
adenohypophysisUBERON:000219679.52gold quality
right hemisphere of cerebellumUBERON:001489079.33gold quality
mucosa of stomachUBERON:000119979.18gold quality
lower esophagus muscularis layerUBERON:003583379.05gold quality
lower esophagusUBERON:001347379.03gold quality
body of uterusUBERON:000985379.01gold quality
corpus callosumUBERON:000233678.87gold quality
cerebellumUBERON:000203778.80gold quality
right ovaryUBERON:000211878.80gold quality
muscle layer of sigmoid colonUBERON:003580578.60gold quality
endocervixUBERON:000045878.57gold quality
rectumUBERON:000105278.57gold quality
stromal cell of endometriumCL:000225578.52gold quality
cortical plateUBERON:000534378.49gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes4.95
E-MTAB-7249no322.70

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

100 targeting ZNF585B, 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-4283100.0066.422097
HSA-MIR-1252-5P100.0069.802774
HSA-MIR-4476100.0068.182030
HSA-MIR-6876-5P100.0067.682126
HSA-MIR-3613-3P100.0076.367965
HSA-MIR-656-3P100.0072.152788
HSA-MIR-4692100.0067.322066
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-451499.9967.101870
HSA-MIR-6870-5P99.9968.552115
HSA-MIR-318599.9968.121959
HSA-MIR-4482-3P99.9872.503147
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-3065-5P99.9771.563281
HSA-MIR-4723-5P99.9768.702034
HSA-MIR-569899.9768.492029
HSA-MIR-7111-5P99.9768.482062
HSA-MIR-314899.9775.066478
HSA-MIR-211099.9666.681930
HSA-MIR-96-5P99.9572.802140
HSA-MIR-651-3P99.9473.485177
HSA-MIR-338-5P99.9272.342951
HSA-MIR-450B-5P99.9271.483175
HSA-MIR-1213399.9271.822006
HSA-MIR-1271-5P99.9171.991972
HSA-MIR-368699.9070.532432
HSA-MIR-6857-5P99.8765.32985
HSA-MIR-391999.8769.452489
HSA-MIR-383-3P99.8565.841359

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 585BQ52M93 (reviewed: Q52M93)

Alternative names: zinc finger protein 41-like protein

All UniProt accessions (7): E9PNT4, E9PQ00, Q52M93, F2Z3L4, K7EL12, K7EP93, K7EPG8

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_689492* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (27 total): zinc finger region 21, chain 1, domain 1, region of interest 1, compositionally biased region 1, sequence variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q52M93-F175.390.03

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 76 (showing top): TGCGCANK_UNKNOWN, NRF2_01, CETS1P54_01, SCGGAAGY_ELK1_02, MGGAAGTG_GABP_B, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, MIKKELSEN_ES_ICP_WITH_H3K4ME3, MIKKELSEN_NPC_ICP_WITH_H3K4ME3, RAO_BOUND_BY_SALL4, CSR_EARLY_UP.V1_DN, CBX7_TARGET_GENES, CIITA_TARGET_GENES, FOXJ2_TARGET_GENES, IRF5_TARGET_GENES, KLF7_TARGET_GENES

GO Biological Process (3): regulation of transcription by RNA polymerase II (GO:0006357), developmental process (GO:0032502), regulation of DNA-templated transcription (GO:0006355)

GO Molecular Function (2): zinc ion binding (GO:0008270), metal ion binding (GO:0046872)

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

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
RNA Polymerase II Transcription1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
regulation of DNA-templated transcription1
transcription by RNA polymerase II1
biological_process1
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
transition metal ion binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

388 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF585BOR4D6Q8NGJ1451
ZNF585BGXYLT1Q4G148415
ZNF585BBEAN1Q3B7T3321
ZNF585BMRPL55Q7Z7F7320
ZNF585BERICH1Q86X53311
ZNF585BSP140LQ9H930307
ZNF585BZBTB3Q9H5J0302
ZNF585BNOL8Q76FK4300
ZNF585BZBTB25P24278294
ZNF585BLHFPL3Q86UP9290
ZNF585BC1orf52Q8N6N3290
ZNF585BCOG5Q9UP83280
ZNF585BRERGLQ9H628270
ZNF585BINO80EQ8NBZ0270
ZNF585BZNF385BQ569K4269

IntAct

9 interactions, top by confidence:

ABTypeScore
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
ZNF585BPCK1psi-mi:“MI:0915”(physical association)0.400
MecomESYT2psi-mi:“MI:0914”(association)0.350
TRIM28ZNF320psi-mi:“MI:0914”(association)0.350
CBX5ZNF568psi-mi:“MI:0914”(association)0.350
ZNF585BhflCpsi-mi:“MI:0915”(physical association)0.000
ZNF585BRIC8Apsi-mi:“MI:0915”(physical association)0.000

BioGRID (7): ZNF585B (Affinity Capture-MS), RIC8A (Two-hybrid), ZNF585B (Affinity Capture-RNA), PCK1 (Affinity Capture-MS), ZNF585B (Affinity Capture-MS), ZNF585B (Co-fractionation), ZNF585B (Affinity Capture-MS)

ESM2 similar proteins: A2VDQ7, A6NNF4, A8MQ14, A8MTY0, E9QAG8, O75290, O75373, P08043, P0CJ79, P10751, P17017, P17027, P17039, P35789, P51522, P51523, Q08AN1, Q14585, Q14587, Q3SYV7, Q3ZCX4, Q4R4C7, Q52M93, Q5MCW4, Q5R5U3, Q5R8X1, Q5R9F0, Q5SXM1, Q6ECI4, Q6JLC9, Q6P3V2, Q6P5C7, Q6ZN57, Q86UE3, Q86XN6, Q86YE8, Q8C827, Q8IYB9, Q8N4W9, Q8N7M2

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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance92
Likely benign11
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1128 predictions. Top by Δscore:

VariantEffectΔscore
19:37190018:GCTTA:Gdonor_loss1.0000
19:37190019:CTTAC:Cdonor_loss1.0000
19:37190020:TTA:Tdonor_loss1.0000
19:37190022:A:ATdonor_loss1.0000
19:37190023:C:Adonor_loss1.0000
19:37190023:CCTA:Cdonor_gain1.0000
19:37190026:A:ACdonor_gain1.0000
19:37190027:C:CCdonor_gain1.0000
19:37210485:T:TAdonor_gain1.0000
19:37210412:A:ACdonor_gain0.9900
19:37210413:C:CCdonor_gain0.9900
19:37210483:AGT:Adonor_gain0.9900
19:37187263:A:Tacceptor_gain0.9800
19:37190022:A:ACdonor_gain0.9800
19:37190023:C:CCdonor_gain0.9800
19:37207178:G:Cdonor_gain0.9800
19:37210405:A:ACdonor_gain0.9800
19:37210460:T:TAdonor_gain0.9800
19:37210523:T:TAdonor_gain0.9800
19:37190152:T:Gacceptor_loss0.9700
19:37190153:G:Cacceptor_loss0.9700
19:37210373:C:CTdonor_gain0.9700
19:37210409:CTGA:Cdonor_gain0.9700
19:37210489:G:Tdonor_gain0.9700
19:37190149:CC:Cacceptor_gain0.9600
19:37190150:CC:Cacceptor_gain0.9600
19:37207251:GAACC:Gacceptor_loss0.9600
19:37207252:AACCT:Aacceptor_loss0.9600
19:37207253:ACCT:Aacceptor_loss0.9600
19:37207254:CCTAG:Cacceptor_loss0.9600

AlphaMissense

5110 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:37185524:A:CF671L0.998
19:37185524:A:TF671L0.998
19:37185526:A:GF671L0.998
19:37185860:G:CF559L0.998
19:37185860:G:TF559L0.998
19:37185862:A:GF559L0.998
19:37185944:A:CF531L0.998
19:37185944:A:TF531L0.998
19:37185946:A:GF531L0.998
19:37186028:G:CF503L0.997
19:37186028:G:TF503L0.997
19:37186030:A:GF503L0.997
19:37185356:A:CF727L0.996
19:37185356:A:TF727L0.996
19:37185358:A:GF727L0.996
19:37185608:A:CF643L0.996
19:37185608:A:TF643L0.996
19:37185610:A:GF643L0.996
19:37185771:C:GR589P0.996
19:37185776:G:CF587L0.996
19:37185776:G:TF587L0.996
19:37185778:A:GF587L0.996
19:37186112:G:CF475L0.996
19:37186112:G:TF475L0.996
19:37186114:A:GF475L0.996
19:37185440:G:CF699L0.995
19:37185440:G:TF699L0.995
19:37185442:A:GF699L0.995
19:37185692:A:CF615L0.995
19:37185692:A:TF615L0.995

dbSNP variants (sampled 300 via entrez): RS1000047061 (19:37195425 C>T), RS1000340447 (19:37183438 G>A,T), RS1000450952 (19:37190488 G>C), RS1000470024 (19:37190785 C>T), RS1000501323 (19:37190571 T>C,G), RS1000590677 (19:37196906 A>C,G), RS1000622238 (19:37195689 T>C), RS1000647071 (19:37203023 A>G), RS1000666358 (19:37189257 C>T), RS1000696364 (19:37202729 G>A), RS1000738952 (19:37190764 C>T), RS1001137949 (19:37201670 A>G), RS1001187740 (19:37188932 GTTC>G), RS1001226366 (19:37183218 T>C), RS1001235688 (19:37190089 T>C)

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

3 associations (top):

StudyTraitp-value
GCST001762_406Obesity-related traits5.000000e-06
GCST007387_24Insomnia symptoms (never/rarely vs. sometimes/usually)5.000000e-08
GCST007388_16Insomnia symptoms (never/rarely vs. usually)8.000000e-10

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0003939energy intake
EFO:0007876insomnia measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

23 total (human), top 23 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arsenitedecreases expression, increases expression3
Air Pollutantsincreases expression, affects expression, increases abundance2
GSK-J4decreases expression1
triphenyl phosphateaffects expression1
propionaldehydeincreases expression1
terbufosincreases methylation1
tobacco tardecreases expression1
nickel sulfatedecreases expression1
avobenzonedecreases expression1
di-n-butylphosphoric acidaffects expression1
CGP 52608affects binding, increases reaction1
Resveratrolincreases expression, affects cotreatment1
Sunitinibdecreases expression1
Benzo(a)pyrenedecreases methylation1
Doxorubicindecreases expression1
Fonofosincreases methylation1
Methotrexateincreases expression1
Ozoneaffects expression, increases abundance1
Parathionincreases methylation1
Plant Extractsaffects cotreatment, increases expression1
Valproic Aciddecreases expression1
Cadmium Chloridedecreases expression1
Particulate Matterincreases abundance, increases expression1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

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

CellosaurusNameCategorySex
CVCL_HD31HEK293 eGFP-ZNF585BTransformed 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.