ZNF578 (zinc finger protein 578) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: ZNF578 (zinc finger protein 578) Homo sapiens
Analyze
Symbol: ZNF578
Name: zinc finger protein 578
RGD ID: 1346407
HGNC Page HGNC:26449
Description: 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 located in cytoplasm. Predicted to be active in nucleus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ31384; Putative chemokine-related protein B42
RGD Orthologs
Bonobo
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381952,453,553 - 52,516,882 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1952,453,553 - 52,516,882 (+)EnsemblGRCh38hg38GRCh38
GRCh371952,956,806 - 53,020,135 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361957,648,641 - 57,711,943 (+)NCBINCBI36Build 36hg18NCBI36
Build 341957,706,024 - 57,708,794NCBI
Celera1950,006,763 - 50,070,083 (+)NCBICelera
Cytogenetic Map19q13.41NCBI
HuRef1949,287,068 - 49,350,657 (+)NCBIHuRef
CHM1_11952,958,517 - 53,021,908 (+)NCBICHM1_1
T2T-CHM13v2.01955,538,104 - 55,601,470 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IEA)
nucleus  (IBA,IEA)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:14702039   PMID:21873635   PMID:25416956   PMID:32296183   PMID:35563538  


Genomics

Comparative Map Data
ZNF578
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381952,453,553 - 52,516,882 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1952,453,553 - 52,516,882 (+)EnsemblGRCh38hg38GRCh38
GRCh371952,956,806 - 53,020,135 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361957,648,641 - 57,711,943 (+)NCBINCBI36Build 36hg18NCBI36
Build 341957,706,024 - 57,708,794NCBI
Celera1950,006,763 - 50,070,083 (+)NCBICelera
Cytogenetic Map19q13.41NCBI
HuRef1949,287,068 - 49,350,657 (+)NCBIHuRef
CHM1_11952,958,517 - 53,021,908 (+)NCBICHM1_1
T2T-CHM13v2.01955,538,104 - 55,601,470 (+)NCBIT2T-CHM13v2.0
ZNF578
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22058,506,190 - 58,569,415 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11960,430,628 - 60,493,796 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01949,406,986 - 49,470,155 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11958,319,947 - 58,341,138 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1958,330,055 - 58,340,361 (+)Ensemblpanpan1.1panPan2

Variants

.
Variants in ZNF578
35 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3 copy number gain See cases [RCV000050883] Chr19:50191219..58535818 [GRCh38]
Chr19:50694476..59047185 [GRCh37]
Chr19:55386288..63738997 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3 copy number gain See cases [RCV000052925] Chr19:49907832..58557889 [GRCh38]
Chr19:50411089..59069256 [GRCh37]
Chr19:55102901..63761068 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3 copy number gain See cases [RCV000052926] Chr19:51141518..58539965 [GRCh38]
Chr19:51644775..59051332 [GRCh37]
Chr19:56336587..63743144 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
NM_001099694.1(ZNF578):c.43C>T (p.Pro15Ser) single nucleotide variant Malignant melanoma [RCV000072313] Chr19:52501888 [GRCh38]
Chr19:53005141 [GRCh37]
Chr19:57696953 [NCBI36]
Chr19:19q13.41		 not provided
NM_001099694.1(ZNF578):c.1645A>C (p.Met549Leu) single nucleotide variant Malignant melanoma [RCV000063616] Chr19:52512026 [GRCh38]
Chr19:53015279 [GRCh37]
Chr19:57707091 [NCBI36]
Chr19:19q13.41		 not provided
NM_001099694.1(ZNF578):c.-121-390T>C single nucleotide variant Lung cancer [RCV000101310] Chr19:52490934 [GRCh38]
Chr19:52994187 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3 copy number gain See cases [RCV000135843] Chr19:50152520..58581203 [GRCh38]
Chr19:50655777..59092570 [GRCh37]
Chr19:55347589..63784382 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3 copy number gain See cases [RCV000142008] Chr19:52143873..58445521 [GRCh38]
Chr19:52647126..58956888 [GRCh37]
Chr19:57338938..63648700 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh37/hg19 19q13.41(chr19:52825019-53017595)x1 copy number loss See cases [RCV000240580] Chr19:52825019..53017595 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:50489390..59095359 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.41(chr19:53002514-53030962)x3 copy number gain See cases [RCV000448858] Chr19:53002514..53030962 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001099694.2(ZNF578):c.496G>C (p.Glu166Gln) single nucleotide variant Inborn genetic diseases [RCV003300318] Chr19:52510877 [GRCh38]
Chr19:53014130 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
NM_001099694.2(ZNF578):c.776A>G (p.Tyr259Cys) single nucleotide variant Inborn genetic diseases [RCV003251478] Chr19:52511157 [GRCh38]
Chr19:53014410 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.8A>G (p.His3Arg) single nucleotide variant Inborn genetic diseases [RCV003279547] Chr19:52501853 [GRCh38]
Chr19:53005106 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3 copy number gain not provided [RCV000740208] Chr19:50740074..59097160 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.41(chr19:52999494-53035705)x3 copy number gain not provided [RCV000740220] Chr19:52999494..53035705 [GRCh37]
Chr19:19q13.41		 benign
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3 copy number gain not provided [RCV001007050] Chr19:44738088..53621561 [GRCh37]
Chr19:19q13.31-13.42		 pathogenic
NM_001099694.2(ZNF578):c.1687G>A (p.Gly563Arg) single nucleotide variant Inborn genetic diseases [RCV003251017] Chr19:52512068 [GRCh38]
Chr19:53015321 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871) copy number gain not provided [RCV001249294] Chr19:47939842..54626871 [GRCh37]
Chr19:19q13.32-13.42		 not provided
GRCh37/hg19 19q13.41(chr19:52987284-53052558)x1 copy number loss not provided [RCV001259946] Chr19:52987284..53052558 [GRCh37]
Chr19:19q13.41		 likely benign
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:48463931..57095254 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438) copy number gain not specified [RCV002052689] Chr19:49911081..53127438 [GRCh37]
Chr19:19q13.33-13.41		 likely pathogenic
NM_001099694.2(ZNF578):c.1285T>G (p.Cys429Gly) single nucleotide variant Inborn genetic diseases [RCV003261351] Chr19:52511666 [GRCh38]
Chr19:53014919 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.17C>T (p.Ala6Val) single nucleotide variant Inborn genetic diseases [RCV002837273] Chr19:52501862 [GRCh38]
Chr19:53005115 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.632A>T (p.Asn211Ile) single nucleotide variant Inborn genetic diseases [RCV002754868] Chr19:52511013 [GRCh38]
Chr19:53014266 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1619A>G (p.Lys540Arg) single nucleotide variant Inborn genetic diseases [RCV002968634] Chr19:52512000 [GRCh38]
Chr19:53015253 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1303G>A (p.Ala435Thr) single nucleotide variant Inborn genetic diseases [RCV002688803] Chr19:52511684 [GRCh38]
Chr19:53014937 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.325G>C (p.Asp109His) single nucleotide variant Inborn genetic diseases [RCV002865014] Chr19:52510706 [GRCh38]
Chr19:53013959 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1144C>G (p.Gln382Glu) single nucleotide variant Inborn genetic diseases [RCV002837078] Chr19:52511525 [GRCh38]
Chr19:53014778 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1387G>C (p.Val463Leu) single nucleotide variant Inborn genetic diseases [RCV002911428] Chr19:52511768 [GRCh38]
Chr19:53015021 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1178A>G (p.His393Arg) single nucleotide variant Inborn genetic diseases [RCV002987101] Chr19:52511559 [GRCh38]
Chr19:53014812 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.380C>G (p.Ala127Gly) single nucleotide variant Inborn genetic diseases [RCV002830647] Chr19:52510761 [GRCh38]
Chr19:53014014 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.205C>T (p.Arg69Cys) single nucleotide variant Inborn genetic diseases [RCV002666379] Chr19:52510586 [GRCh38]
Chr19:53013839 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001099694.2(ZNF578):c.131C>T (p.Ala44Val) single nucleotide variant Inborn genetic diseases [RCV002893171] Chr19:52504722 [GRCh38]
Chr19:53007975 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1505G>A (p.Arg502His) single nucleotide variant Inborn genetic diseases [RCV002764499] Chr19:52511886 [GRCh38]
Chr19:53015139 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1356G>T (p.Glu452Asp) single nucleotide variant Inborn genetic diseases [RCV002675095] Chr19:52511737 [GRCh38]
Chr19:53014990 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1756C>G (p.Pro586Ala) single nucleotide variant Inborn genetic diseases [RCV002813640] Chr19:52512137 [GRCh38]
Chr19:53015390 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1012A>G (p.Thr338Ala) single nucleotide variant Inborn genetic diseases [RCV003008624] Chr19:52511393 [GRCh38]
Chr19:53014646 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.949T>C (p.Cys317Arg) single nucleotide variant Inborn genetic diseases [RCV002988230] Chr19:52511330 [GRCh38]
Chr19:53014583 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1106A>G (p.Lys369Arg) single nucleotide variant Inborn genetic diseases [RCV003184470] Chr19:52511487 [GRCh38]
Chr19:53014740 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1535A>T (p.Lys512Met) single nucleotide variant Inborn genetic diseases [RCV003205011] Chr19:52511916 [GRCh38]
Chr19:53015169 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1084C>T (p.Arg362Cys) single nucleotide variant Inborn genetic diseases [RCV003260411] Chr19:52511465 [GRCh38]
Chr19:53014718 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.437A>G (p.His146Arg) single nucleotide variant Inborn genetic diseases [RCV003208077] Chr19:52510818 [GRCh38]
Chr19:53014071 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1668C>G (p.Asn556Lys) single nucleotide variant Inborn genetic diseases [RCV003208380] Chr19:52512049 [GRCh38]
Chr19:53015302 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.1732C>T (p.His578Tyr) single nucleotide variant Inborn genetic diseases [RCV003305143] Chr19:52512113 [GRCh38]
Chr19:53015366 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.749A>G (p.Gln250Arg) single nucleotide variant Inborn genetic diseases [RCV003372225] Chr19:52511130 [GRCh38]
Chr19:53014383 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.387G>C (p.Met129Ile) single nucleotide variant Inborn genetic diseases [RCV003347762] Chr19:52510768 [GRCh38]
Chr19:53014021 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001099694.2(ZNF578):c.476G>C (p.Ser159Thr) single nucleotide variant Inborn genetic diseases [RCV003363695] Chr19:52510857 [GRCh38]
Chr19:53014110 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:49625130..57647352 [GRCh37]
Chr19:19q13.33-13.43		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:475
Count of miRNA genes:388
Interacting mature miRNAs:414
Transcripts:ENST00000421239, ENST00000594118, ENST00000596382, ENST00000596674, ENST00000601120, ENST00000602221
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH39501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371952,955,143 - 52,955,294UniSTSGRCh37
GRCh371548,634,222 - 48,634,377UniSTSGRCh37
Build 361546,421,514 - 46,421,669RGDNCBI36
Celera1950,005,076 - 50,005,227UniSTS
Celera1525,526,689 - 25,526,844RGD
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map19q13.41UniSTS
HuRef1949,285,381 - 49,285,532UniSTS
HuRef1525,467,222 - 25,467,377UniSTS
D19S651E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371953,019,888 - 53,020,036UniSTSGRCh37
Build 361957,711,700 - 57,711,848RGDNCBI36
Celera1950,069,840 - 50,069,988RGD
Cytogenetic Map19q13.41UniSTS
HuRef1949,350,414 - 49,350,562UniSTS
GeneMap99-GB4 RH Map19278.34UniSTS
D5S2354  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q21UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map12q24.11UniSTS
D7S3207  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map2q31.2-q33.1UniSTS
D16S325  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map10q11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3q13.32UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map2p13-p12UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map8q21.13UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map1p36.3-p34.3UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19q13.4UniSTS
UniSTS:481881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371953,014,233 - 53,015,545UniSTSGRCh37
Celera1950,064,184 - 50,065,496UniSTS
HuRef1949,344,757 - 49,346,069UniSTS
UniSTS:484132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371953,014,223 - 53,015,582UniSTSGRCh37
Celera1950,064,174 - 50,065,533UniSTS
HuRef1949,344,747 - 49,346,106UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 4 1
Low 283 232 819 21 344 23 869 176 761 71 981 958 1 118 583 3
Below cutoff 2117 2669 798 498 1332 338 3455 1998 2923 305 435 599 167 1085 2198 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001099694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438189 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319853 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319854 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319855 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319856 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB091373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB091374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB091375 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB091376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC022150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK095562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC103904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC115704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX955279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000421239   ⟹   ENSP00000459216
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,453,553 - 52,516,882 (+)Ensembl
RefSeq Acc Id: ENST00000601120   ⟹   ENSP00000470790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,492,830 - 52,511,142 (+)Ensembl
RefSeq Acc Id: NM_001099694   ⟹   NP_001093164
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,453,553 - 52,516,882 (+)NCBI
GRCh371952,956,829 - 53,020,131 (+)RGD
GRCh371952,956,829 - 53,020,131 (+)NCBI
Build 361957,648,641 - 57,711,943 (+)NCBI Archive
Celera1950,006,763 - 50,070,083 (+)RGD
HuRef1949,287,068 - 49,350,657 (+)ENTREZGENE
CHM1_11952,958,517 - 53,021,908 (+)NCBI
T2T-CHM13v2.01955,538,104 - 55,601,470 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001366182   ⟹   NP_001353111
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,453,553 - 52,516,882 (+)NCBI
T2T-CHM13v2.01955,538,104 - 55,601,470 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047438189   ⟹   XP_047294145
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,453,553 - 52,516,882 (+)NCBI
RefSeq Acc Id: XM_047438190   ⟹   XP_047294146
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,489,977 - 52,516,882 (+)NCBI
RefSeq Acc Id: XM_047438191   ⟹   XP_047294147
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,486,443 - 52,516,882 (+)NCBI
RefSeq Acc Id: XM_047438192   ⟹   XP_047294148
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,490,358 - 52,516,882 (+)NCBI
RefSeq Acc Id: XM_047438193   ⟹   XP_047294149
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,492,804 - 52,516,882 (+)NCBI
RefSeq Acc Id: XM_047438194   ⟹   XP_047294150
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,453,553 - 52,516,882 (+)NCBI
RefSeq Acc Id: XM_054319850   ⟹   XP_054175825
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,538,104 - 55,601,470 (+)NCBI
RefSeq Acc Id: XM_054319851   ⟹   XP_054175826
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,538,104 - 55,601,470 (+)NCBI
RefSeq Acc Id: XM_054319852   ⟹   XP_054175827
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,574,559 - 55,601,470 (+)NCBI
RefSeq Acc Id: XM_054319853   ⟹   XP_054175828
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,571,033 - 55,601,470 (+)NCBI
RefSeq Acc Id: XM_054319854   ⟹   XP_054175829
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,574,947 - 55,601,470 (+)NCBI
RefSeq Acc Id: XM_054319855   ⟹   XP_054175830
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,577,331 - 55,601,470 (+)NCBI
RefSeq Acc Id: XM_054319856   ⟹   XP_054175831
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,577,362 - 55,601,470 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001093164 (Get FASTA)   NCBI Sequence Viewer  
  NP_001353111 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294145 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294146 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294147 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294148 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294149 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294150 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175825 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175826 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175827 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175828 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175829 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175830 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175831 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI03905 (Get FASTA)   NCBI Sequence Viewer  
  AAI15705 (Get FASTA)   NCBI Sequence Viewer  
  BAB71051 (Get FASTA)   NCBI Sequence Viewer  
  BAC04574 (Get FASTA)   NCBI Sequence Viewer  
  BAE93189 (Get FASTA)   NCBI Sequence Viewer  
  BAE93190 (Get FASTA)   NCBI Sequence Viewer  
  BAE93191 (Get FASTA)   NCBI Sequence Viewer  
  BAE93192 (Get FASTA)   NCBI Sequence Viewer  
  BAG61163 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000459216
  ENSP00000459216.1
  ENSP00000470790.1
GenBank Protein Q1T7F1 (Get FASTA)   NCBI Sequence Viewer  
  Q96N58 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001093164   ⟸   NM_001099694
- UniProtKB: B4DR51 (UniProtKB/Swiss-Prot),   I3L1Y6 (UniProtKB/Swiss-Prot),   Q96N58 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001353111   ⟸   NM_001366182
- UniProtKB: Q96N58 (UniProtKB/Swiss-Prot),   B4DR51 (UniProtKB/Swiss-Prot),   I3L1Y6 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: ENSP00000470790   ⟸   ENST00000601120
RefSeq Acc Id: ENSP00000459216   ⟸   ENST00000421239
RefSeq Acc Id: XP_047294145   ⟸   XM_047438189
- Peptide Label: isoform X1
- UniProtKB: Q96N58 (UniProtKB/Swiss-Prot),   B4DR51 (UniProtKB/Swiss-Prot),   I3L1Y6 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047294150   ⟸   XM_047438194
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047294147   ⟸   XM_047438191
- Peptide Label: isoform X1
- UniProtKB: Q96N58 (UniProtKB/Swiss-Prot),   B4DR51 (UniProtKB/Swiss-Prot),   I3L1Y6 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047294146   ⟸   XM_047438190
- Peptide Label: isoform X1
- UniProtKB: Q96N58 (UniProtKB/Swiss-Prot),   B4DR51 (UniProtKB/Swiss-Prot),   I3L1Y6 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047294148   ⟸   XM_047438192
- Peptide Label: isoform X1
- UniProtKB: Q96N58 (UniProtKB/Swiss-Prot),   B4DR51 (UniProtKB/Swiss-Prot),   I3L1Y6 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047294149   ⟸   XM_047438193
- Peptide Label: isoform X1
- UniProtKB: Q96N58 (UniProtKB/Swiss-Prot),   B4DR51 (UniProtKB/Swiss-Prot),   I3L1Y6 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054175826   ⟸   XM_054319851
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175825   ⟸   XM_054319850
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175828   ⟸   XM_054319853
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175827   ⟸   XM_054319852
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175829   ⟸   XM_054319854
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175830   ⟸   XM_054319855
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175831   ⟸   XM_054319856
- Peptide Label: isoform X2
Protein Domains
C2H2-type   KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q1T7F1-F1-model_v2 AlphaFold Q1T7F1 1-81 view protein structure
AF-Q96N58-F1-model_v2 AlphaFold Q96N58 1-590 view protein structure

Promoters
RGD ID:13205475
Promoter ID:EPDNEW_H26318
Type:initiation region
Name:ZNF578_1
Description:zinc finger protein 578
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,453,576 - 52,453,636EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26449 AgrOrtholog
COSMIC ZNF578 COSMIC
Ensembl Genes ENSG00000258405 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000421239 ENTREZGENE
  ENST00000421239.7 UniProtKB/Swiss-Prot
  ENST00000601120.1 UniProtKB/TrEMBL
Gene3D-CATH 6.10.140.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000258405 GTEx
HGNC ID HGNC:26449 ENTREZGENE
Human Proteome Map ZNF578 Human Proteome Map
InterPro KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KRAB_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:147660 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 147660 ENTREZGENE
PANTHER KRAB DOMAIN C2H2 ZINC FINGER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KRAB DOMAIN-CONTAINING PROTEIN 5-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC FINGER PROTEIN 728-LIKE UniProtKB/TrEMBL
  ZINC FINGER PROTEIN ZIC AND GLI UniProtKB/TrEMBL
Pfam KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2_6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134936072 PharmGKB
PROSITE KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF109640 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B4DR51 ENTREZGENE
  CCB42_HUMAN UniProtKB/Swiss-Prot
  I3L1Y6 ENTREZGENE
  M0QZV4_HUMAN UniProtKB/TrEMBL
  Q1T7F1 ENTREZGENE
  Q3MI94_HUMAN UniProtKB/TrEMBL
  Q96N58 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B4DR51 UniProtKB/Swiss-Prot
  I3L1Y6 UniProtKB/Swiss-Prot
  Q1LZM9 UniProtKB/TrEMBL