ZNF135

gene
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Also known as pHZ-17

Summary

ZNF135 (zinc finger protein 135, HGNC:12919) is a protein-coding gene on chromosome 19q13.43, encoding Zinc finger protein 135 (P52742). Plays a role in the regulation of cell morphology and cytoskeletal organization.

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. Predicted to be active in nucleus.

Source: NCBI Gene 7694 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 114 total
  • MANE Select transcript: NM_001289401

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:12919
Approved symbolZNF135
Namezinc finger protein 135
Location19q13.43
Locus typegene with protein product
StatusApproved
AliasespHZ-17
Ensembl geneENSG00000176293
Ensembl biotypeprotein_coding
OMIM604077
Entrez7694

Gene structure

Transcript identifiers

Ensembl transcripts: 11 — 10 protein_coding, 1 nonsense_mediated_decay

ENST00000313434, ENST00000359978, ENST00000401053, ENST00000506786, ENST00000511556, ENST00000515535, ENST00000890101, ENST00000890102, ENST00000890103, ENST00000890104, ENST00000938056

RefSeq mRNA: 7 — MANE Select: NM_001289401 NM_001164527, NM_001164529, NM_001164530, NM_001289401, NM_001289402, NM_003436, NM_007134

CCDS: CCDS12970, CCDS54329, CCDS54330, CCDS74471, CCDS74472

Canonical transcript exons

ENST00000313434 — 5 exons

ExonStartEnd
ENSE000013535705805996958060035
ENSE000013535775805928258059310
ENSE000017192545806344658063541
ENSE000020196075806674158069755
ENSE000035848715806158058061706

Expression profiles

Bgee: expression breadth ubiquitous, 186 present calls, max score 89.09.

FANTOM5 (CAGE): breadth broad, TPM avg 1.5642 / max 45.8352, expressed in 652 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1778111.3989606
2089500.165385

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099189.09gold quality
ganglionic eminenceUBERON:000402385.29gold quality
cortical plateUBERON:000534384.11gold quality
endothelial cellCL:000011583.52silver quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.57gold quality
left ovaryUBERON:000211979.79gold quality
ventricular zoneUBERON:000305379.58gold quality
right lobe of thyroid glandUBERON:000111978.77gold quality
right ovaryUBERON:000211878.29gold quality
right uterine tubeUBERON:000130278.12gold quality
left lobe of thyroid glandUBERON:000112077.96gold quality
thyroid glandUBERON:000204676.99gold quality
ovaryUBERON:000099276.79gold quality
body of uterusUBERON:000985376.78gold quality
apex of heartUBERON:000209876.16gold quality
adenohypophysisUBERON:000219675.63gold quality
stromal cell of endometriumCL:000225575.53gold quality
pituitary glandUBERON:000000775.43gold quality
endocervixUBERON:000045875.17gold quality
left uterine tubeUBERON:000130375.05gold quality
right coronary arteryUBERON:000162574.68gold quality
ectocervixUBERON:001224974.54gold quality
lower esophagus muscularis layerUBERON:003583374.40gold quality
lower esophagusUBERON:001347374.36gold quality
popliteal arteryUBERON:000225074.17gold quality
C1 segment of cervical spinal cordUBERON:000646974.17gold quality
tibial arteryUBERON:000761074.16gold quality
hair follicleUBERON:000207374.15gold quality
right testisUBERON:000453474.11gold quality
islet of LangerhansUBERON:000000674.08gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no3.22

Regulation

Is transcription factor: yes

Downstream targets (CollecTRI)

2 targets.

TargetRegulation
CADM1
CDKN2A

JASPAR motifs

MotifNameFamily
MA1587.1ZNF135More than 3 adjacent zinc fingers

JASPAR matrix evidence (PMIDs): PMID:28092692

miRNA regulators (miRDB)

47 targeting ZNF135, 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-450A-1-3P100.0069.331837
HSA-MIR-548AW99.9972.573559
HSA-MIR-1229-3P99.9766.49906
HSA-MIR-570-3P99.9672.414910
HSA-MIR-1468-3P99.9672.743797
HSA-MIR-6744-5P99.9366.82748
HSA-MIR-6508-5P99.9270.672465
HSA-MIR-7-1-3P99.9171.534384
HSA-MIR-7-2-3P99.9171.404394
HSA-MIR-10523-5P99.9169.222038
HSA-MIR-1211999.8768.351653
HSA-MIR-576-5P99.8470.462582
HSA-MIR-44899.7972.372103
HSA-MIR-548AJ-5P99.7871.123085
HSA-MIR-548G-5P99.7871.123085
HSA-MIR-548X-5P99.7871.123085
HSA-MIR-548F-5P99.7871.023093
HSA-MIR-4524A-3P99.7266.852406
HSA-MIR-3158-5P99.6567.511763
HSA-MIR-4762-5P99.5768.541424
HSA-MIR-182-3P99.5767.57825
HSA-MIR-6716-5P99.5668.621244
HSA-MIR-186-3P99.5166.241685
HSA-MIR-135A-5P99.3671.851601
HSA-MIR-135B-5P99.3671.631613
HSA-MIR-3678-3P99.3167.101432
HSA-MIR-504-3P99.3067.181745
HSA-MIR-7151-3P99.0469.722370
HSA-MIR-1213598.9970.261814
HSA-MIR-629-5P98.7868.721032

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 135P52742 (reviewed: P52742)

Alternative names: Zinc finger protein 61, Zinc finger protein 78-like 1

All UniProt accessions (3): P52742, M0R0N7, Q8N9M3

UniProt curated annotations — full annotation on UniProt →

Function. Plays a role in the regulation of cell morphology and cytoskeletal organization. May be involved in transcriptional regulation.

Subcellular location. Nucleus.

Miscellaneous. May be due to competing acceptor splice site.

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

Isoforms (4)

UniProt IDNamesCanonical?
P52742-11yes
P52742-22
P52742-33
P52742-44

RefSeq proteins (7): NP_001157999, NP_001158001, NP_001158002, NP_001276330, NP_001276331, NP_003427, NP_009065 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (30 total): zinc finger region 16, sequence variant 5, splice variant 3, sequence conflict 3, chain 1, domain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P52742-F173.590.31

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 101 (showing top): GOBP_REGULATION_OF_CELL_MORPHOGENESIS, BROWNE_HCMV_INFECTION_48HR_DN, BROWNE_HCMV_INFECTION_14HR_DN, MULLIGHAN_NPM1_SIGNATURE_3_DN, GRADE_COLON_AND_RECTAL_CANCER_DN, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, MULLIGHAN_NPM1_MUTATED_SIGNATURE_1_DN, BAE_BRCA1_TARGETS_DN, PURBEY_TARGETS_OF_CTBP1_NOT_SATB1_UP, E2F3_UP.V1_DN, SRC_UP.V1_DN, NFE2L2.V2, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, MIR570_3P, MIR4795_3P

GO Biological Process (6): regulation of transcription by RNA polymerase II (GO:0006357), cytoskeleton organization (GO:0007010), regulation of cell morphogenesis (GO:0022604), regulation of DNA-templated transcription (GO:0006355), regulation of anatomical structure morphogenesis (GO:0022603), negative regulation of DNA-templated transcription (GO:0045892)

GO Molecular Function (6): 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), 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 transcription2
DNA-templated transcription2
RNA polymerase II transcription regulatory region sequence-specific DNA binding2
transcription by RNA polymerase II1
organelle organization1
cell morphogenesis1
regulation of anatomical structure morphogenesis1
regulation of gene expression1
regulation of RNA biosynthetic process1
anatomical structure morphogenesis1
regulation of developmental process1
negative regulation of RNA biosynthetic process1
cis-regulatory region sequence-specific DNA binding1
chromatin1
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

402 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF135MAGEB10Q96LZ2398
ZNF135ITPRID1Q6ZRS4372
ZNF135GPATCH2LQ9NWQ4351
ZNF135ADHFE1Q8IWW8318
ZNF135MAGEB3O15480317
ZNF135LRRIQ1Q96JM4302
ZNF135MYO15BQ96JP2300
ZNF135HTATIP2Q9BUP3290
ZNF135EML3Q32P44290
ZNF135CARD8Q9Y2G2290
ZNF135PPP1R3EQ9H7J1289
ZNF135TMEM25Q86YD3272
ZNF135CCDC124Q96CT7272
ZNF135MAGEF1Q9HAY2271
ZNF135MAGEB18Q96M61270
ZNF135FAM163AQ96GL9270

IntAct

20 interactions, top by confidence:

ABTypeScore
ZNF135LMO4psi-mi:“MI:0915”(physical association)0.560
ZNF135SCNM1psi-mi:“MI:0915”(physical association)0.560
ZNF135ANKS1Apsi-mi:“MI:0915”(physical association)0.560
ZNF135WWOXpsi-mi:“MI:0915”(physical association)0.560
ZNF135psi-mi:“MI:0915”(physical association)0.370
ANXA7ZNF135psi-mi:“MI:0915”(physical association)0.370
ZNF135CDKN1Apsi-mi:“MI:0915”(physical association)0.370
ZNF135GADD45Apsi-mi:“MI:0915”(physical association)0.370
GSK3BZNF135psi-mi:“MI:0915”(physical association)0.370
ZNF135RAP1Bpsi-mi:“MI:0915”(physical association)0.370
ZNF135RCC1psi-mi:“MI:0915”(physical association)0.370
WWOXZNF135psi-mi:“MI:0915”(physical association)0.000
LMO4ZNF135psi-mi:“MI:0915”(physical association)0.000
SCNM1ZNF135psi-mi:“MI:0915”(physical association)0.000
ANKS1AZNF135psi-mi:“MI:0915”(physical association)0.000

BioGRID (11): ZNF135 (Two-hybrid), ZNF135 (Two-hybrid), ZNF135 (Two-hybrid), WWOX (Two-hybrid), ZNF135 (Affinity Capture-RNA), ZNF135 (Two-hybrid), ZNF135 (Two-hybrid), ZNF135 (Two-hybrid), ZNF135 (Two-hybrid), ZNF135 (Two-hybrid), ZNF135 (Two-hybrid)

ESM2 similar proteins: A2VDQ7, A6NN14, A8MQ14, A8MTY0, B7Z6K7, E9QAG8, O75290, O75373, P08043, P0CJ79, P10751, P17017, P17035, P17039, P18745, P18751, P35789, P51522, P51523, P52742, Q02386, Q08AN1, Q14585, Q14587, Q3SYV7, Q4R4C7, Q5R5U3, Q5R8X1, Q5R9F0, Q5SXM1, Q6P5C7, Q6ZN06, Q6ZN57, Q86UE3, Q86XN6, Q8IYB9, Q8N4W9, Q8N7M2, Q8N7Q3, Q8N972

Diamond homologs: A0JPL0, A1L1L7, A2A761, A2VDP4, A3KN36, A6QLU5, A6QPT6, A7MBI1, A8MT65, B2RXC5, E9PYI1, E9Q8G5, O75290, O94892, O95780, P10076, P17014, P17023, P17025, P17030, P17032, P17098, P51523, P51814, P52736, P52742, P58317, Q02975, Q06730, Q06732, Q08DG8, Q0VCB0, Q13360, Q14584, Q14587, Q14590, Q147U1, Q16587, Q29RZ4, Q2M218

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance94
Likely benign5
Benign6

Top pathogenic / likely-pathogenic (0)

SpliceAI

1172 predictions. Top by Δscore:

VariantEffectΔscore
19:58061702:TGTGG:Tdonor_loss1.0000
19:58061703:GTGG:Gdonor_gain1.0000
19:58061705:GG:Gdonor_gain1.0000
19:58061705:GGGT:Gdonor_loss1.0000
19:58061706:GG:Gdonor_gain1.0000
19:58061706:GGTAA:Gdonor_loss1.0000
19:58061707:G:GCdonor_loss1.0000
19:58061708:TAA:Tdonor_loss1.0000
19:58086168:CCTCA:Cdonor_loss1.0000
19:58086169:CTCA:Cdonor_loss1.0000
19:58086170:TCA:Tdonor_loss1.0000
19:58086171:CAC:Cdonor_loss1.0000
19:58086187:T:TAdonor_gain1.0000
19:58086262:ATACC:Aacceptor_gain1.0000
19:58086263:TACC:Tacceptor_gain1.0000
19:58086264:ACC:Aacceptor_gain1.0000
19:58086264:ACCC:Aacceptor_loss1.0000
19:58086265:CC:Cacceptor_gain1.0000
19:58086265:CCC:Cacceptor_gain1.0000
19:58086266:CC:Cacceptor_gain1.0000
19:58086267:C:CCacceptor_gain1.0000
19:58086267:C:Tacceptor_gain1.0000
19:58086271:G:Cacceptor_gain1.0000
19:58086271:G:GCacceptor_gain1.0000
19:58086276:G:Cacceptor_gain1.0000
19:58086276:G:GCacceptor_gain1.0000
19:58086277:T:Cacceptor_gain1.0000
19:58086277:T:TCacceptor_gain1.0000
19:58086285:C:CTacceptor_gain1.0000
19:58059306:GGAGG:Gdonor_gain0.9900

AlphaMissense

4378 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:58067487:T:CF335L0.999
19:58067489:C:AF335L0.999
19:58067489:C:GF335L0.999
19:58067571:T:CF363L0.999
19:58067573:C:AF363L0.999
19:58067573:C:GF363L0.999
19:58067655:T:CF391L0.999
19:58067657:C:AF391L0.999
19:58067657:C:GF391L0.999
19:58067739:T:CF419L0.999
19:58067741:C:AF419L0.999
19:58067741:C:GF419L0.999
19:58067403:T:CF307L0.998
19:58067405:C:AF307L0.998
19:58067405:C:GF307L0.998
19:58067506:T:CL341P0.998
19:58067516:T:AH344Q0.998
19:58067516:T:GH344Q0.998
19:58067605:G:CR374P0.998
19:58067907:T:CF475L0.998
19:58067909:C:AF475L0.998
19:58067909:C:GF475L0.998
19:58067991:T:CF503L0.998
19:58067993:C:AF503L0.998
19:58067993:C:GF503L0.998
19:58068159:T:CF559L0.998
19:58068161:C:AF559L0.998
19:58068161:C:GF559L0.998
19:58067235:T:CF251L0.997
19:58067237:C:AF251L0.997

dbSNP variants (sampled 300 via entrez): RS1000007384 (19:58062497 C>G,T), RS1000038573 (19:58062733 C>T), RS1000100401 (19:58062260 C>G,T), RS1001012788 (19:58069879 T>C), RS1001044296 (19:58066522 T>C), RS1001052817 (19:58058220 G>A,C), RS1001677741 (19:58060863 G>A), RS1001710686 (19:58061086 C>T), RS1002201440 (19:58066049 A>G), RS1002232334 (19:58066262 C>T), RS1003239205 (19:58064697 T>A), RS1003392654 (19:58059809 C>A,G), RS1003487903 (19:58059541 A>G), RS1003812937 (19:58062865 A>C), RS1004155942 (19:58057245 T>C)

Disease associations

OMIM: gene MIM:604077 | 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

16 total (human), top 16 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, increases methylation2
GSK-J4decreases expression1
triphenyl phosphateaffects expression1
sodium arsenitedecreases expression1
Resveratrolincreases expression1
Sunitinibincreases expression1
Benzo(a)pyreneaffects methylation1
Cadmiumdecreases expression, increases abundance1
Bucladesineaffects cotreatment, increases expression1
Estradiolaffects cotreatment, increases expression1
Niclosamideincreases expression1
Tobacco Smoke Pollutiondecreases expression1
Medroxyprogesterone Acetateaffects cotreatment, increases expression1
Sodium Selenitedecreases expression1
Cadmium Chlorideincreases abundance, decreases expression1
Acrylamidedecreases expression1

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.