ZNF157

gene
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Also known as HZF22

Summary

ZNF157 (zinc finger protein 157, HGNC:12942) is a protein-coding gene on chromosome Xp11.3, encoding Zinc finger protein 157 (P51786). May be involved in transcriptional regulation.

This gene product is a likely zinc finger family transcription factor. It contains KRAB-A and KRAB-B domains that act as transcriptional repressors in related proteins, and multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. This gene is part of a gene cluster on chromosome Xp11.23.

Source: NCBI Gene 7712 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 82 total
  • MANE Select transcript: NM_003446

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:12942
Approved symbolZNF157
Namezinc finger protein 157
LocationXp11.3
Locus typegene with protein product
StatusApproved
AliasesHZF22
Ensembl geneENSG00000147117
Ensembl biotypeprotein_coding
OMIM300024
Entrez7712

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000377073

RefSeq mRNA: 1 — MANE Select: NM_003446 NM_003446

CCDS: CCDS14278

Canonical transcript exons

ENST00000377073 — 4 exons

ExonStartEnd
ENSE000013911784741068047410775
ENSE000014726994741236947414498
ENSE000014727014737057847370740
ENSE000017902524741027647410402

Expression profiles

Bgee: expression breadth broad, 93 present calls, max score 68.52.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
cortical plateUBERON:000534368.52gold quality
endometrium epitheliumUBERON:000481165.68gold quality
ventricular zoneUBERON:000305364.69gold quality
ganglionic eminenceUBERON:000402364.40gold quality
right uterine tubeUBERON:000130261.83gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099161.77gold quality
olfactory segment of nasal mucosaUBERON:000538661.66gold quality
islet of LangerhansUBERON:000000659.58gold quality
cerebellar cortexUBERON:000212959.14gold quality
cerebellar hemisphereUBERON:000224559.11gold quality
embryoUBERON:000092257.87gold quality
cerebellumUBERON:000203757.86gold quality
right hemisphere of cerebellumUBERON:001489057.72gold quality
adenohypophysisUBERON:000219655.19gold quality
prefrontal cortexUBERON:000045154.78gold quality
pituitary glandUBERON:000000754.14gold quality
paraflocculusUBERON:000535152.72gold quality
fallopian tubeUBERON:000388952.26gold quality
lymph nodeUBERON:000002951.98gold quality
nasal cavity mucosaUBERON:000182651.20gold quality
thymusUBERON:000237051.16silver quality
stromal cell of endometriumCL:000225551.10silver quality
smooth muscle tissueUBERON:000113550.54gold quality
frontal poleUBERON:000279550.41gold quality
middle frontal gyrusUBERON:000270250.30gold quality
Brodmann (1909) area 10UBERON:001354150.18gold quality
frontal cortexUBERON:000187050.01gold quality
quadriceps femorisUBERON:000137749.95gold quality
neocortexUBERON:000195049.72gold quality
vastus lateralisUBERON:000137949.56gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.26
E-GEOD-83139no24.51

Regulation

Is transcription factor: yes

JASPAR motifs

MotifNameFamily
MA2331.1ZNF157More than 3 adjacent zinc fingers

JASPAR matrix evidence (PMIDs): PMID:28273063

Upstream regulators (CollecTRI, top): STAT1

miRNA regulators (miRDB)

4 targeting ZNF157, 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-6715B-5P99.6469.631420
HSA-MIR-426999.5569.891373
HSA-MIR-64098.4466.93644
HSA-MIR-3085-5P97.7265.43544

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), ZNF182 (ENSG00000147118), ZNF41 (ENSG00000147124), ZNF7 (ENSG00000147789), ZNF117 (ENSG00000152926), ZNF221 (ENSG00000159905), ZNF235 (ENSG00000159917), ZNF714 (ENSG00000160352), ZNF577 (ENSG00000161551), ZNF12 (ENSG00000164631), ZNF3 (ENSG00000166526)

Protein

Protein identifiers

Zinc finger protein 157P51786 (reviewed: P51786)

Alternative names: Zinc finger protein HZF22

All UniProt accessions (1): P51786

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_003437* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (15 total): zinc finger region 12, chain 1, domain 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P51786-F176.240.39

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 102 (showing top): MORF_FLT1, MORF_MSH3, MORF_BRCA1, MORF_ESR1, MORF_RAD51L3, MORF_CTSB, MORF_IL4, MORF_PRKCA, CAR_MYST2, MODULE_123, MODULE_157, CAR_MLANA, MORF_THPO, MODULE_113, MORF_ATF2

GO Biological Process (3): regulation of DNA-templated transcription (GO:0006355), regulation of macromolecule metabolic process (GO:0060255), regulation of primary metabolic process (GO:0080090)

GO Molecular Function (3): DNA binding (GO:0003677), 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 metabolic process2
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
macromolecule metabolic process1
primary metabolic process1
nucleic acid binding1
transition metal ion binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

482 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF157ARAFP07557813
ZNF157CTSVO60911671
ZNF157TIMP1P01033667
ZNF157CD99P14209545
ZNF157TMEM63AO94886509
ZNF157UBA1P22314506
ZNF157TIMP3P35625490
ZNF157CTSSP25774473
ZNF157GNB3P16520427
ZNF157PRSS8Q16651426
ZNF157DCAF12L2Q5VW00418
ZNF157SCNN1AP37088418
ZNF157SPANXN4Q5MJ08417
ZNF157PPP1R1BQ9UD71391
ZNF157PTGER3P43115387

IntAct

3 interactions, top by confidence:

ABTypeScore
ZNF157EDF1psi-mi:“MI:0915”(physical association)0.400
ZNF157ECHS1psi-mi:“MI:0915”(physical association)0.400

BioGRID (9): ZNF157 (Affinity Capture-MS), ZNF157 (Affinity Capture-MS), ZNF157 (Affinity Capture-MS), ZNF157 (Affinity Capture-MS), ZNF157 (Affinity Capture-MS), ZNF157 (Affinity Capture-MS), ZNF157 (Proximity Label-MS), ZNF157 (Proximity Label-MS), ZNF157 (Cross-Linking-MS (XL-MS))

ESM2 similar proteins: A2RRD8, A6NHJ4, B4DX44, O75346, P10077, P10755, P15621, P16372, P16373, P51786, P52737, P85977, Q0VGE8, Q14588, Q147U1, Q15928, Q15973, Q2M3X9, Q3KNS6, Q3MIS6, Q494X3, Q5HY98, Q5RBQ3, Q5REK1, Q5VIY5, Q60585, Q61751, Q6GQR8, Q7L2R6, Q7TSH9, Q8IYX0, Q8N782, Q8N823, Q8N988, Q8N9F8, Q8NA42, Q8NCK3, Q8NDP4, Q8NEP9, Q8TC21

Diamond homologs: A0A1W2PQL4, A0JNB1, A0JPL0, A6NK53, A6QLU5, A6QPT6, A7MBI1, A8MT65, A8MUV8, A8MWA4, B2RXC5, B4DU55, B4DX44, E9PYI1, O14628, O75346, P0CH99, P0CI00, P17014, P17030, P17032, P17098, P51786, P85977, Q02386, Q06730, Q06732, Q0VAW7, Q12901, Q13360, Q14586, Q14588, Q14590, Q16587, Q2M3X9, Q2VY69, Q32M78, Q3ZCX4, Q49AA0, Q4R6J4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance54
Likely benign4
Benign5

Top pathogenic / likely-pathogenic (0)

SpliceAI

1226 predictions. Top by Δscore:

VariantEffectΔscore
X:47370737:TGAGG:Tdonor_loss1.0000
X:47370740:GGTA:Gdonor_loss1.0000
X:47370741:GTA:Gdonor_loss1.0000
X:47370742:T:Gdonor_loss1.0000
X:47410274:A:ACacceptor_loss1.0000
X:47410274:A:AGacceptor_gain1.0000
X:47410274:AGG:Aacceptor_gain1.0000
X:47410275:G:GAacceptor_loss1.0000
X:47410275:G:GGacceptor_gain1.0000
X:47410275:GGG:Gacceptor_gain1.0000
X:47410363:G:GTdonor_gain1.0000
X:47410398:TGTGG:Tdonor_loss1.0000
X:47410399:GTGG:Gdonor_gain1.0000
X:47410401:GG:Gdonor_gain1.0000
X:47410402:GG:Gdonor_gain1.0000
X:47410403:G:GGdonor_gain1.0000
X:47410403:GT:Gdonor_loss1.0000
X:47410404:T:Adonor_loss1.0000
X:47410408:G:GTdonor_gain1.0000
X:47410771:CTCAG:Cdonor_gain1.0000
X:47410772:TCAG:Tdonor_gain1.0000
X:47410774:AG:Adonor_gain1.0000
X:47410775:GG:Gdonor_gain1.0000
X:47410776:G:GGdonor_gain1.0000
X:47370738:GAG:Gdonor_gain0.9900
X:47370741:G:GGdonor_gain0.9900
X:47381250:G:GTdonor_gain0.9900
X:47407208:C:Gdonor_gain0.9900
X:47410274:AG:Aacceptor_gain0.9900
X:47410274:AGGG:Aacceptor_gain0.9900

AlphaMissense

3355 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
X:47412836:T:CF255L0.999
X:47412838:T:AF255L0.999
X:47412838:T:GF255L0.999
X:47412752:T:CF227L0.998
X:47412754:T:AF227L0.998
X:47412754:T:GF227L0.998
X:47412855:T:CL261P0.998
X:47412668:T:CF199L0.997
X:47412670:C:AF199L0.997
X:47412670:C:GF199L0.997
X:47412771:T:CL233P0.997
X:47412863:C:GH264D0.997
X:47412867:A:CQ265P0.997
X:47412920:T:CF283L0.997
X:47412922:T:AF283L0.997
X:47412922:T:GF283L0.997
X:47413004:T:CF311L0.997
X:47413006:C:AF311L0.997
X:47413006:C:GF311L0.997
X:47412793:C:AH240Q0.996
X:47412793:C:GH240Q0.996
X:47412877:C:AH268Q0.996
X:47412877:C:GH268Q0.996
X:47412939:T:CL289P0.996
X:47412687:T:CL205P0.995
X:47412781:T:AH236Q0.995
X:47412781:T:GH236Q0.995
X:47412837:T:CF255S0.995
X:47412863:C:AH264N0.995
X:47412865:T:AH264Q0.995

dbSNP variants (sampled 300 via entrez): RS1000254993 (X:47385965 T>A), RS1000304895 (X:47370891 G>C), RS1000366766 (X:47370221 A>G), RS1000420853 (X:47373782 C>G), RS1000517864 (X:47393519 T>C), RS1000905952 (X:47369023 A>C,G), RS1000923321 (X:47410301 C>A), RS1000954104 (X:47410722 G>A), RS1001012921 (X:47395595 T>C), RS1001040503 (X:47396052 C>T), RS1001120175 (X:47409612 C>T), RS1001130608 (X:47401976 G>A,T), RS1001342391 (X:47386656 C>T), RS1001397734 (X:47381660 G>A), RS1001423035 (X:47376346 G>T)

Disease associations

OMIM: gene MIM:300024 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

1 associations (top):

StudyTraitp-value
GCST000657_7Optic nerve measurement (disc area)4.000000e-07

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
bisphenol Aaffects cotreatment, increases expression1
arseniteincreases methylation1
sodium arsenitedecreases expression1
Decitabineincreases expression1
Benzo(a)pyrenedecreases methylation1
Dexamethasoneaffects cotreatment, increases expression1
Indomethacinaffects cotreatment, increases expression1
Niclosamideincreases expression1
Tobacco Smoke Pollutiondecreases expression1
1-Methyl-3-isobutylxanthineaffects cotreatment, increases expression1
Aflatoxin B1decreases methylation1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

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

CellosaurusNameCategorySex
CVCL_XW10HEK293 eGFP-ZNF157Transformed 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.