ZNF169

gene
On this page

Also known as MGC51961

Summary

ZNF169 (zinc finger protein 169, HGNC:12957) is a protein-coding gene on chromosome 9q22.32, encoding Zinc finger protein 169 (Q14929). 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 169841 — RefSeq curated summary.

At a glance

  • GWAS associations: 9
  • Clinical variants (ClinVar): 90 total
  • MANE Select transcript: NM_194320

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:12957
Approved symbolZNF169
Namezinc finger protein 169
Location9q22.32
Locus typegene with protein product
StatusApproved
AliasesMGC51961
Ensembl geneENSG00000175787
Ensembl biotypeprotein_coding
OMIM603404
Entrez169841

Gene structure

Transcript identifiers

Ensembl transcripts: 10 — 9 protein_coding, 1 retained_intron

ENST00000340911, ENST00000395395, ENST00000480716, ENST00000481550, ENST00000492115, ENST00000718459, ENST00000718460, ENST00000873354, ENST00000873355, ENST00000873356

RefSeq mRNA: 3 — MANE Select: NM_194320 NM_001301275, NM_003448, NM_194320

CCDS: CCDS6709

Canonical transcript exons

ENST00000395395 — 5 exons

ExonStartEnd
ENSE000014211239429981594301829
ENSE000018539489425929894259345
ENSE000035487419429234194292467
ENSE000036162009427875894278845
ENSE000036720459429297494293069

Expression profiles

Bgee: expression breadth ubiquitous, 219 present calls, max score 89.75.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 2.2778 / max 29.2792, expressed in 1148 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
974532.27781148

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
parotid glandUBERON:000183189.75silver quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047381.80gold quality
monocyteCL:000057680.21gold quality
subthalamic nucleusUBERON:000190680.14gold quality
cardia of stomachUBERON:000116279.77gold quality
leukocyteCL:000073879.70gold quality
rectumUBERON:000105279.54gold quality
lateral nuclear group of thalamusUBERON:000273678.33silver quality
dorsal plus ventral thalamusUBERON:000189777.85gold quality
lateral globus pallidusUBERON:000247677.80silver quality
right uterine tubeUBERON:000130277.02gold quality
right ovaryUBERON:000211876.73gold quality
left ovaryUBERON:000211976.58gold quality
inferior vagus X ganglionUBERON:000536376.41gold quality
vena cavaUBERON:000408776.18silver quality
endocervixUBERON:000045876.14gold quality
prefrontal cortexUBERON:000045176.12gold quality
ventral tegmental areaUBERON:000269176.08gold quality
small intestine Peyer’s patchUBERON:000345476.03gold quality
lymph nodeUBERON:000002975.88gold quality
body of uterusUBERON:000985375.77gold quality
right coronary arteryUBERON:000162575.65gold quality
tibial nerveUBERON:000132375.58gold quality
right lobe of thyroid glandUBERON:000111975.48gold quality
tracheaUBERON:000312675.48gold quality
transverse colonUBERON:000115775.44gold quality
ectocervixUBERON:001224975.41gold quality
saliva-secreting glandUBERON:000104475.35gold quality
substantia nigra pars compactaUBERON:000196575.26gold quality
metanephros cortexUBERON:001053375.25gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no3.99

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): STAT1

miRNA regulators (miRDB)

14 targeting ZNF169, 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-4476100.0068.182030
HSA-MIR-6876-5P100.0067.682126
HSA-MIR-8485100.0077.574731
HSA-MIR-806299.8868.43995
HSA-MIR-394199.8670.542735
HSA-MIR-451799.7669.191867
HSA-MIR-497-3P99.6169.711990
HSA-MIR-4753-5P99.5468.511356
HSA-MIR-154-5P98.9266.65733
HSA-MIR-1245B-5P98.8866.55576
HSA-MIR-314298.8866.09529
HSA-MIR-361198.7668.761290
HSA-MIR-4733-3P98.3565.20994
HSA-MIR-6849-3P97.2564.571371

Literature-anchored findings (GeneRIF, showing 1)

  • Overexpression of ZNF169 promotes the growth and proliferation of colorectal cancer cells via the upregulation of ANKZF1. (PMID:38666541)

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
mus_musculusZfp169ENSMUSG00000050954
rattus_norvegicusZfp169ENSRNOG00000017092
drosophila_melanogasterCG2712FBGN0024975
drosophila_melanogasterPhsFBGN0036522
drosophila_melanogasterCG3281FBGN0260741

Paralogs (62): ZNF582 (ENSG00000018869), ZNF264 (ENSG00000083844), ZNF343 (ENSG00000088876), ZNF684 (ENSG00000117010), ZNF133 (ENSG00000125846), ZNF557 (ENSG00000130544), ZNF337 (ENSG00000130684), ZNF20 (ENSG00000132010), ZFP37 (ENSG00000136866), ZNF614 (ENSG00000142556), KRBOX4 (ENSG00000147121), ZNF599 (ENSG00000153896), ZNF19 (ENSG00000157429), ZNF589 (ENSG00000164048), PRDM9 (ENSG00000164256), ZNF180 (ENSG00000167384), ZNF558 (ENSG00000167785), ZNF35 (ENSG00000169981), ZNF778 (ENSG00000170100), ZNF439 (ENSG00000171291), ZNF440 (ENSG00000171295), ZNF556 (ENSG00000172000), ZNF554 (ENSG00000172006), ZNF596 (ENSG00000172748), ZNF80 (ENSG00000174255), ZNF266 (ENSG00000174652), ZNF25 (ENSG00000175395), ZNF77 (ENSG00000175691), ZNF404 (ENSG00000176222), ZNF491 (ENSG00000177599), ZNF620 (ENSG00000177842), ZNF619 (ENSG00000177873), ZNF875 (ENSG00000181666), ZNF329 (ENSG00000181894), ZFP90 (ENSG00000184939), ZNF566 (ENSG00000186017), ZNF529 (ENSG00000186020), ZNF749 (ENSG00000186230), ZNF555 (ENSG00000186300), ZNF70 (ENSG00000187792)

Protein

Protein identifiers

Zinc finger protein 169Q14929 (reviewed: Q14929)

All UniProt accessions (4): Q14929, Q5SR55, Q7Z761, S4R440

UniProt curated annotations — full annotation on UniProt →

Function. May be involved in transcriptional regulation.

Subcellular location. Nucleus.

Tissue specificity. Highly expressed in kidney, weakly expressed in heart, liver, spleen, and small intestine. Not expressed in adult brain or spinal cord.

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

RefSeq proteins (3): NP_001288204, NP_003439, NP_919301* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050752C2H2-ZF_domainFamily

Pfam: PF00096, PF01352

UniProt features (30 total): zinc finger region 13, sequence conflict 7, sequence variant 5, region of interest 2, chain 1, domain 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q14929-F172.110.41

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 54 (showing top): chr9q22, URS_ADIPOCYTE_DIFFERENTIATION_DN, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ASH1L_TARGET_GENES, DLX4_TARGET_GENES, DMRT1_TARGET_GENES, ELF2_TARGET_GENES, FEV_TARGET_GENES, PAX3_TARGET_GENES, SUPT16H_TARGET_GENES, ZSCAN2_TARGET_GENES, MIR3941, MIR6876_5P, MIR4476

GO Biological Process (2): regulation of transcription by RNA polymerase II (GO:0006357), regulation of DNA-templated transcription (GO:0006355)

GO Molecular Function (6): 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), DNA binding (GO:0003677), protein binding (GO:0005515), 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
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
transcription cis-regulatory region binding1
chromatin1
RNA polymerase II transcription regulatory region sequence-specific DNA binding1
DNA-binding transcription factor activity1
regulation of transcription by RNA polymerase II1
transition metal ion binding1
nucleic acid binding1
binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

628 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF169ASS1P00966750
ZNF169FANCCQ00597624
ZNF169XPAP23025581
ZNF169TGFBR1P36897574
ZNF169PTCH1Q13635529
ZNF169ATP13A4Q4VNC1508
ZNF169NUTM2GQ5VZR2473
ZNF169SLC67A1Q96BI1457
ZNF169GJA10Q969M2452
ZNF169SLC38A4Q969I6449
ZNF169HHATQ5VTY9449
ZNF169NUTM2FA1L443448
ZNF169CFAP210Q0VFZ6448
ZNF169DUSP22Q9NRW4441
ZNF169AGPAT2O15120432

IntAct

19 interactions, top by confidence:

ABTypeScore
CCNDBP1ZNF169psi-mi:“MI:0915”(physical association)0.560
KRTAP10-7ZNF169psi-mi:“MI:0915”(physical association)0.560
ZNF169CEP70psi-mi:“MI:0915”(physical association)0.560
ZNF169CCNDBP1psi-mi:“MI:0915”(physical association)0.560
ZNF169KRTAP10-7psi-mi:“MI:0915”(physical association)0.560
KRTAP10-6ZNF169psi-mi:“MI:0915”(physical association)0.560
ZNF169CABP5psi-mi:“MI:0915”(physical association)0.560
ZNF169ZNF316psi-mi:“MI:0914”(association)0.530
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
ZNF169KRTAP10-6psi-mi:“MI:0915”(physical association)0.000
CABP5ZNF169psi-mi:“MI:0915”(physical association)0.000

BioGRID (85): ZNF169 (Two-hybrid), ZNF169 (Two-hybrid), KRTAP10-7 (Two-hybrid), ZNF169 (Affinity Capture-MS), C10orf2 (Affinity Capture-MS), RBAK (Affinity Capture-MS), SOGA1 (Affinity Capture-MS), ZYG11A (Affinity Capture-MS), ZNF92 (Affinity Capture-MS), SORL1 (Affinity Capture-MS), ZNF689 (Affinity Capture-MS), ZBTB10 (Affinity Capture-MS), ZNF445 (Affinity Capture-MS), TRIM41 (Affinity Capture-MS), TRIM26 (Affinity Capture-MS)

ESM2 similar proteins: A3KN32, A3KN36, O14709, O43296, O75123, P15622, P16373, P17023, P17031, P17097, P52736, P85977, Q07230, Q12901, Q14929, Q29RZ4, Q4V8A8, Q571J5, Q5CZA5, Q5JNZ3, Q5R7I8, Q5RBX0, Q5RBY9, Q5RCD9, Q5RCX4, Q61751, Q61967, Q6GQR8, Q6IV72, Q6NX45, Q6PK81, Q6ZMS4, Q7TNU6, Q7TSH9, Q7Z398, Q7Z7L9, Q8BI99, Q8BIQ3, Q8BLB0, Q8IZ26

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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance82
Likely benign4
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

819 predictions. Top by Δscore:

VariantEffectΔscore
9:94278754:CCAG:Cacceptor_loss1.0000
9:94278757:GATTT:Gacceptor_gain1.0000
9:94278842:GGAG:Gdonor_gain1.0000
9:94278843:GAG:Gdonor_gain1.0000
9:94278843:GAGG:Gdonor_gain1.0000
9:94278844:AGGTA:Adonor_loss1.0000
9:94278845:GGTA:Gdonor_loss1.0000
9:94278846:G:GAdonor_loss1.0000
9:94278846:G:GGdonor_gain1.0000
9:94278847:T:Adonor_loss1.0000
9:94292335:TTACA:Tacceptor_loss1.0000
9:94292339:A:AGacceptor_gain1.0000
9:94292339:AG:Aacceptor_gain1.0000
9:94292340:G:GTacceptor_gain1.0000
9:94292340:GG:Gacceptor_gain1.0000
9:94292340:GGC:Gacceptor_gain1.0000
9:94292340:GGCA:Gacceptor_gain1.0000
9:94292340:GGCAT:Gacceptor_gain1.0000
9:94292428:G:Tdonor_gain1.0000
9:94292434:A:AGdonor_gain1.0000
9:94292466:GG:Gdonor_gain1.0000
9:94292467:GG:Gdonor_gain1.0000
9:94292468:G:Adonor_loss1.0000
9:94292468:G:GGdonor_gain1.0000
9:94292469:T:Gdonor_loss1.0000
9:94292965:T:TAacceptor_gain1.0000
9:94292967:T:TAacceptor_gain1.0000
9:94292971:TAGGA:Tacceptor_loss1.0000
9:94292972:A:Gacceptor_loss1.0000
9:94292973:G:GTacceptor_loss1.0000

AlphaMissense

3953 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
9:94300537:T:CF327L0.999
9:94300539:T:AF327L0.999
9:94300539:T:GF327L0.999
9:94300621:T:CF355L0.999
9:94300623:T:AF355L0.999
9:94300623:T:GF355L0.999
9:94300873:T:CF439L0.999
9:94300875:T:AF439L0.999
9:94300875:T:GF439L0.999
9:94300957:T:CF467L0.999
9:94300959:T:AF467L0.999
9:94300959:T:GF467L0.999
9:94300369:T:CF271L0.997
9:94300371:T:AF271L0.997
9:94300371:T:GF271L0.997
9:94300453:T:CF299L0.997
9:94300455:C:AF299L0.997
9:94300455:C:GF299L0.997
9:94300789:T:CF411L0.997
9:94300791:T:AF411L0.997
9:94300791:T:GF411L0.997
9:94300874:T:CF439S0.997
9:94300538:T:CF327S0.996
9:94300705:T:CF383L0.996
9:94300707:C:AF383L0.996
9:94300707:C:GF383L0.996
9:94300734:C:AH392Q0.996
9:94300734:C:GH392Q0.996
9:94300892:T:CL445P0.996
9:94300902:C:AH448Q0.996

dbSNP variants (sampled 300 via entrez): RS1000223284 (9:94269146 T>C), RS1000264404 (9:94260982 G>A), RS1000273346 (9:94276580 A>G), RS1000488597 (9:94282226 T>G), RS1000506612 (9:94268206 A>G), RS1000607420 (9:94274864 C>T), RS1000698369 (9:94260711 G>A), RS1000737627 (9:94273984 A>C), RS1000744311 (9:94277718 T>G), RS1000845877 (9:94298685 C>T), RS1000874510 (9:94263089 T>A,C), RS1000938007 (9:94293937 G>A), RS1001024954 (9:94273780 C>T), RS1001038723 (9:94294443 GA>G,GAA), RS1001137898 (9:94258123 C>G,T)

Disease associations

OMIM: gene MIM:603404 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

9 associations (top):

StudyTraitp-value
GCST001416_9Body mass index (SNP x SNP interaction)6.000000e-07
GCST004904_45Body mass index3.000000e-09
GCST004904_63Body mass index2.000000e-09
GCST006222_3Cerebellum growth1.000000e-06
GCST008128_5Body mass index9.000000e-10
GCST009379_90Type 2 diabetes2.000000e-09
GCST009379_91Type 2 diabetes3.000000e-06
GCST90002396_410Mean reticulocyte volume4.000000e-29
GCST90002397_687Mean spheric corpuscular volume3.000000e-13

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0004340body mass index
EFO:0010701mean reticulocyte volume

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

9 total (human), top 9 by PubMed support.

ChemicalActions (top 5)PubMed papers
Tobacco Smoke Pollutiondecreases expression, increases expression2
Cadmium Chloridedecreases expression2
TAK-243increases sumoylation1
bisphenol Adecreases methylation1
(+)-JQ1 compounddecreases expression1
Arsenicaffects methylation1
Benzo(a)pyreneincreases methylation1
Okadaic Aciddecreases expression1
Acrylamidedecreases expression1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

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

CellosaurusNameCategorySex
CVCL_XW11HEK293 eGFP-ZNF169Transformed 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.