ZNF665

gene
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Also known as FLJ14345ZFP160L

Summary

ZNF665 (zinc finger protein 665, HGNC:25885) is a protein-coding gene on chromosome 19q13.42, encoding Zinc finger protein 665 (Q9H7R5). May be involved in transcriptional regulation.

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-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 79788 — RefSeq curated summary.

At a glance

  • GWAS associations: 3
  • Clinical variants (ClinVar): 127 total
  • MANE Select transcript: NM_024733

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25885
Approved symbolZNF665
Namezinc finger protein 665
Location19q13.42
Locus typegene with protein product
StatusApproved
AliasesFLJ14345, ZFP160L
Ensembl geneENSG00000197497
Ensembl biotypeprotein_coding
Entrez79788

Gene structure

Transcript identifiers

Ensembl transcripts: 11 — 7 protein_coding, 4 protein_coding_CDS_not_defined

ENST00000396424, ENST00000596373, ENST00000596564, ENST00000597544, ENST00000598440, ENST00000600412, ENST00000650736, ENST00000868912, ENST00000868913, ENST00000958707, ENST00000958708

RefSeq mRNA: 4 — MANE Select: NM_024733 NM_001353457, NM_001353458, NM_001353459, NM_024733

CCDS: CCDS46169

Canonical transcript exons

ENST00000396424 — 4 exons

ExonStartEnd
ENSE000025225165317544553175571
ENSE000030978575316242453166347
ENSE000031310035319331253193358
ENSE000035728155318288453182943

Expression profiles

Bgee: expression breadth ubiquitous, 255 present calls, max score 93.34.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 3.1438 / max 54.2742, expressed in 1239 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1825553.14381239

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
corpus epididymisUBERON:000435993.34gold quality
buccal mucosa cellCL:000233693.30gold quality
caput epididymisUBERON:000435893.24gold quality
cauda epididymisUBERON:000436092.84gold quality
medial globus pallidusUBERON:000247790.98gold quality
globus pallidusUBERON:000187589.20gold quality
pancreatic ductal cellCL:000207989.07gold quality
tendon of biceps brachiiUBERON:000818888.80silver quality
postcentral gyrusUBERON:000258188.20gold quality
cartilage tissueUBERON:000241888.07silver quality
superficial temporal arteryUBERON:000161487.66gold quality
bronchial epithelial cellCL:000232887.30gold quality
epithelial cell of pancreasCL:000008387.07silver quality
parietal lobeUBERON:000187286.49gold quality
olfactory bulbUBERON:000226486.23gold quality
adult organismUBERON:000702386.15gold quality
myocardiumUBERON:000234986.02silver quality
heart right ventricleUBERON:000208086.00silver quality
diaphragmUBERON:000110385.94silver quality
oocyteCL:000002385.86gold quality
type B pancreatic cellCL:000016985.72silver quality
skin of hipUBERON:000155485.70gold quality
epithelium of bronchusUBERON:000203185.31gold quality
Brodmann (1909) area 46UBERON:000648385.30gold quality
bronchusUBERON:000218585.10gold quality
mammary ductUBERON:000176585.00gold quality
secondary oocyteCL:000065584.94gold quality
mammalian vulvaUBERON:000099784.61silver quality
pigmented layer of retinaUBERON:000178284.49gold quality
thymusUBERON:000237084.09silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-MTAB-8410yes19.58
E-ANND-3no5.72

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

48 targeting ZNF665, 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-513A-5P100.0069.772465
HSA-MIR-453199.9969.703181
HSA-MIR-477599.9875.006394
HSA-MIR-3065-5P99.9771.563281
HSA-MIR-590-3P99.9674.346478
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-9983-3P99.9471.483631
HSA-MIR-95-5P99.8972.173973
HSA-MIR-6875-3P99.8270.262983
HSA-MIR-3913-3P99.7466.53938
HSA-MIR-430699.7270.503630
HSA-MIR-518A-5P99.7069.012209
HSA-MIR-52799.7069.012209
HSA-MIR-6516-3P99.6568.571238
HSA-MIR-4743-3P99.6268.122095
HSA-MIR-18A-3P99.5665.681092
HSA-MIR-190A-5P99.5471.45933
HSA-MIR-190B-5P99.5471.40925
HSA-MIR-7159-5P99.5372.122472
HSA-MIR-1213199.4868.721673
HSA-MIR-4728-3P99.4768.94981
HSA-MIR-312399.4767.152693
HSA-MIR-318299.4068.152454
HSA-MIR-185-5P99.3568.602497
HSA-MIR-464499.3569.122514
HSA-MIR-155-5P99.3570.161509
HSA-MIR-504-3P99.3067.181745
HSA-MIR-6504-3P99.1769.312891
HSA-MIR-7151-3P99.0469.722370
HSA-MIR-607498.8969.642187

Cross-species orthologs

32 orthologs

OrganismSymbolGene ID
danio_rerioznf646ENSDARG00000061424
danio_reriosi:dkey-154p10.3ENSDARG00000068366
danio_reriosi:dkey-89b17.4ENSDARG00000075545
danio_reriozgc:66472ENSDARG00000075916
danio_reriosi:ch211-148l7.4ENSDARG00000094469
danio_rerioznf576.1ENSDARG00000097819
mus_musculusZfp160ENSMUSG00000067942
rattus_norvegicusZfp160ENSRNOG00000059492
drosophila_melanogasterSry-deltaFBGN0003512
drosophila_melanogasteraz2FBGN0025185
drosophila_melanogasterhangFBGN0026575
drosophila_melanogasterCG3032FBGN0029928
drosophila_melanogasterCG2129FBGN0030008
drosophila_melanogasterCG11695FBGN0030316
drosophila_melanogasterCG8944FBGN0030680
drosophila_melanogasterCG7101FBGN0030963
drosophila_melanogasterCG1602FBGN0033186
drosophila_melanogasterCG18011FBGN0033491
drosophila_melanogasterCG12942FBGN0033569
drosophila_melanogasterCG8089FBGN0033993
drosophila_melanogasterindraFBGN0035213
drosophila_melanogasterCG10654FBGN0036294
drosophila_melanogasterCG6791FBGN0037918
drosophila_melanogasterCG17803FBGN0038547
drosophila_melanogasterCG12219FBGN0043796
drosophila_melanogasterCG30020FBGN0050020
drosophila_melanogasterpzgFBGN0259785
drosophila_melanogastermldFBGN0263490
drosophila_melanogasterzf30CFBGN0270924
caenorhabditis_elegansztf-15WBGENE00011066
caenorhabditis_elegansWBGENE00013734
caenorhabditis_elegansWBGENE00015649

Paralogs (36): ZNF302 (ENSG00000089335), ZNF184 (ENSG00000096654), CTCF (ENSG00000102974), ZNF574 (ENSG00000105732), ZBTB24 (ENSG00000112365), ZNF142 (ENSG00000115568), CTCFL (ENSG00000124092), ZNF473 (ENSG00000142528), ZNF827 (ENSG00000151612), ZNF689 (ENSG00000156853), ZNF208 (ENSG00000160321), ZNF91 (ENSG00000167232), ZNF526 (ENSG00000167625), ZNF764 (ENSG00000169951), ZNF747 (ENSG00000169955), ZNF282 (ENSG00000170265), ZNF160 (ENSG00000170949), ZNF497 (ENSG00000174586), ZBTB34 (ENSG00000177125), ZNF771 (ENSG00000179965), ZNF48 (ENSG00000180035), ZNF594 (ENSG00000180626), ZBTB37 (ENSG00000185278), ZFP92 (ENSG00000189420), ZNF107 (ENSG00000196247), ZNF729 (ENSG00000196350), ZNF569 (ENSG00000196437), ZNF420 (ENSG00000197050), ZNF785 (ENSG00000197162), ZNF181 (ENSG00000197841), ZNF347 (ENSG00000197937), ZNF84 (ENSG00000198040), ZBTB48 (ENSG00000204859), ZNF845 (ENSG00000213799), ZNF99 (ENSG00000213973), ZNF688 (ENSG00000229809)

Protein

Protein identifiers

Zinc finger protein 665Q9H7R5 (reviewed: Q9H7R5)

Alternative names: Zinc finger protein 160-like

All UniProt accessions (2): A0A3Q5AD24, Q9H7R5

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 (4): NP_001340386, NP_001340387, NP_001340388, NP_079009* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050331Zinc_finger_PRDM4/PRDM1/PRDM14Family

Pfam: PF00096, PF01352

UniProt features (24 total): zinc finger region 18, sequence variant 3, chain 1, domain 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9H7R5-F173.100.09

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 48 (showing top): GOCC_NUCLEOLUS, YOSHIMURA_MAPK8_TARGETS_UP, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOBP_NEGATIVE_REGULATION_OF_NUCLEOBASE_CONTAINING_COMPOUND_METABOLIC_PROCESS, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, MIR4306, MIR513A_5P, MIR190A_5P, MIR190B_5P, MIR215_3P, MIR96_3P, GSE13411_NAIVE_BCELL_VS_PLASMA_CELL_UP, GSE13411_IGM_MEMORY_BCELL_VS_PLASMA_CELL_UP, GSE1460_NAIVE_CD4_TCELL_ADULT_BLOOD_VS_THYMIC_STROMAL_CELL_UP, GSE15659_NAIVE_CD4_TCELL_VS_RESTING_TREG_DN

GO Biological Process (3): regulation of transcription by RNA polymerase II (GO:0006357), negative regulation of DNA-templated transcription (GO:0045892), regulation of DNA-templated transcription (GO:0006355)

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), sequence-specific DNA binding (GO:0043565), metal ion binding (GO:0046872)

GO Cellular Component (3): nucleus (GO:0005634), nucleolus (GO:0005730), microtubule cytoskeleton (GO:0015630)

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
negative regulation of RNA biosynthetic process1
regulation of gene expression1
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
DNA binding1
cation binding1
intracellular membrane-bounded organelle1
nuclear lumen1
intracellular membraneless organelle1
cytoskeleton1

Protein interactions and networks

STRING

442 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF665KRABD2Q6ZNG9431
ZNF665TMEM74BQ9NUR3393
ZNF665ARMH4Q86TY3366
ZNF665RSKRQ96LW2360
ZNF665SYDE2Q5VT97349
ZNF665DENND4BO75064348
ZNF665LRATD1Q96KN4327
ZNF665RETREG3Q86VR2324
ZNF665TTC36A6NLP5323
ZNF665DUSP18Q8NEJ0322
ZNF665RNF145Q96MT1314
ZNF665KLHL5Q96PQ7308
ZNF665N4BP2Q86UW6300
ZNF665OTOGLQ3ZCN5296
ZNF665TPTE2Q6XPS3287

IntAct

4 interactions, top by confidence:

ABTypeScore
NEK4E2F8psi-mi:“MI:0914”(association)0.350
Mpsi-mi:“MI:0914”(association)0.350
ZNF665pepPpsi-mi:“MI:0915”(physical association)0.000

BioGRID (2): ZNF665 (Affinity Capture-MS), ZNF665 (Proximity Label-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: A0A1W2PQL4, A2RRD8, A2VDQ7, A6NHJ4, A6NK75, A6NN14, A6NNF4, A6NP11, B4DX44, B4DXR9, E9PW05, O14628, O43345, O75290, O75346, O75373, O75820, P0CB33, P0CJ79, P0DKX0, P10755, P17032, P17035, P52738, Q02386, Q03923, Q03936, Q05481, Q08AN1, Q09FC8, Q0VGE8, Q14586, Q14593, Q147U1, Q15928, Q3MIS6, Q3SXZ3, Q494X3, Q4R6C2, Q5HY98

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance109
Likely benign13
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1403 predictions. Top by Δscore:

VariantEffectΔscore
19:53166344:ATATC:Aacceptor_loss1.0000
19:53166347:TCTG:Tacceptor_loss1.0000
19:53166348:C:CAacceptor_loss1.0000
19:53166349:T:Aacceptor_loss1.0000
19:53175438:T:TAdonor_gain1.0000
19:53175484:C:Adonor_gain1.0000
19:53175567:TGTCC:Tacceptor_gain1.0000
19:53175570:CC:Cacceptor_gain1.0000
19:53175571:CC:Cacceptor_gain1.0000
19:53175571:CCTAA:Cacceptor_loss1.0000
19:53175572:C:CCacceptor_gain1.0000
19:53175572:CT:Cacceptor_loss1.0000
19:53175573:T:Gacceptor_loss1.0000
19:53166343:GATAT:Gacceptor_gain0.9900
19:53166345:TAT:Tacceptor_gain0.9900
19:53166348:C:CCacceptor_gain0.9900
19:53175440:CTCA:Cdonor_loss0.9900
19:53175441:TCACC:Tdonor_loss0.9900
19:53175442:CACCC:Cdonor_loss0.9900
19:53175443:AC:Adonor_gain0.9900
19:53175444:C:CTdonor_loss0.9900
19:53175444:CC:Cdonor_gain0.9900
19:53175460:T:TAdonor_gain0.9900
19:53175483:T:TAdonor_gain0.9900
19:53175568:GTCC:Gacceptor_gain0.9900
19:53193310:A:ACdonor_gain0.9900
19:53193311:C:CCdonor_gain0.9900
19:53193311:CG:Cdonor_gain0.9900
19:53193311:CGCGG:Cdonor_gain0.9900
19:53166344:ATAT:Aacceptor_gain0.9800

AlphaMissense

4518 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:53164585:G:CF635L0.998
19:53164585:G:TF635L0.998
19:53164587:A:GF635L0.998
19:53164669:G:CF607L0.998
19:53164669:G:TF607L0.998
19:53164671:A:GF607L0.998
19:53165173:A:CF439L0.997
19:53165173:A:TF439L0.997
19:53165175:A:GF439L0.997
19:53165341:G:CF383L0.997
19:53165341:G:TF383L0.997
19:53165343:A:GF383L0.997
19:53165509:A:CF327L0.997
19:53165509:A:TF327L0.997
19:53165511:A:GF327L0.997
19:53165593:G:CF299L0.997
19:53165593:G:TF299L0.997
19:53165595:A:GF299L0.997
19:53165677:A:CF271L0.997
19:53165677:A:TF271L0.997
19:53165679:A:GF271L0.997
19:53164501:A:CF663L0.996
19:53164501:A:TF663L0.996
19:53164503:A:GF663L0.996
19:53164753:A:CF579L0.996
19:53164753:A:TF579L0.996
19:53164755:A:GF579L0.996
19:53164921:A:CF523L0.996
19:53164921:A:TF523L0.996
19:53164923:A:GF523L0.996

dbSNP variants (sampled 300 via entrez): RS1000268467 (19:53191708 G>A), RS1000301168 (19:53191462 T>C), RS1000315901 (19:53179561 C>T), RS1000355836 (19:53192965 G>A), RS1000477979 (19:53171184 C>G), RS1000568432 (19:53167071 G>A), RS1000599231 (19:53192819 G>A), RS1000630286 (19:53192682 A>C), RS1000647140 (19:53181025 A>G), RS1000762290 (19:53185446 G>A), RS1000824442 (19:53194462 A>G), RS1000870151 (19:53175633 C>T), RS1000893437 (19:53193181 A>G), RS1000976715 (19:53189733 A>G), RS1001050502 (19:53169072 C>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

3 associations (top):

StudyTraitp-value
GCST001508_5Asthma4.000000e-06
GCST003026_6Yu-Zhi constitution type in type 2 diabetes5.000000e-06
GCST006298_5Response to haloperidol in schizophrenia7.000000e-06

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0007638Yu-Zhi constitution type

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

11 total (human), top 11 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneincreases expression, increases methylation, increases mutagenesis, affects methylation, decreases expression4
Arsenicaffects methylation, increases methylation2
Valproic Aciddecreases expression2
GSK-J4decreases expression1
triphenyl phosphateaffects expression1
arseniteincreases methylation1
sodium arseniteincreases expression1
di-n-butylphosphoric acidaffects expression1
Sunitinibincreases expression1
Tobacco Smoke Pollutiondecreases expression1
Vitamin Edecreases 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.