ZNF843 (zinc finger protein 843) - 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: ZNF843 (zinc finger protein 843) Homo sapiens
Analyze
Symbol: ZNF843
Name: zinc finger protein 843
RGD ID: 2300359
HGNC Page HGNC:28710
Description: Predicted to enable metal ion binding activity.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: MGC46336
RGD Orthologs
Bonobo
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381631,435,434 - 31,443,160 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1631,432,593 - 31,443,160 (-)EnsemblGRCh38hg38GRCh38
GRCh371631,446,755 - 31,454,481 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361631,354,386 - 31,361,849 (-)NCBINCBI36Build 36hg18NCBI36
Celera1628,854,038 - 28,861,497 (+)NCBICelera
Cytogenetic Map16p11.2NCBI
HuRef1629,007,272 - 29,014,730 (-)NCBIHuRef
CHM1_11632,765,512 - 32,772,971 (-)NCBICHM1_1
T2T-CHM13v2.01631,822,848 - 31,830,569 (-)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

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:22939624   PMID:25036637   PMID:28514442   PMID:32296183   PMID:33961781  


Genomics

Comparative Map Data
ZNF843
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381631,435,434 - 31,443,160 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1631,432,593 - 31,443,160 (-)EnsemblGRCh38hg38GRCh38
GRCh371631,446,755 - 31,454,481 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361631,354,386 - 31,361,849 (-)NCBINCBI36Build 36hg18NCBI36
Celera1628,854,038 - 28,861,497 (+)NCBICelera
Cytogenetic Map16p11.2NCBI
HuRef1629,007,272 - 29,014,730 (-)NCBIHuRef
CHM1_11632,765,512 - 32,772,971 (-)NCBICHM1_1
T2T-CHM13v2.01631,822,848 - 31,830,569 (-)NCBIT2T-CHM13v2.0
ZNF843
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21834,643,993 - 34,645,392 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11639,439,671 - 39,452,931 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01623,522,907 - 23,530,912 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11631,805,809 - 31,828,619 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1631,805,098 - 31,807,111 (-)Ensemblpanpan1.1panPan2
ZNF843
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1528,131,522 - 28,142,641 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660681,297,505 - 1,305,248 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in ZNF843
24 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16p11.2-11.1(chr16:30691912-36160463)x3 copy number gain See cases [RCV000133811] Chr16:30691912..36160463 [GRCh38]
Chr16:30703233..35147508 [GRCh37]
Chr16:30610734..35005009 [NCBI36]
Chr16:16p11.2-11.1		 pathogenic
GRCh38/hg38 16p11.2(chr16:29909613-31438697)x3 copy number gain See cases [RCV000135339] Chr16:29909613..31438697 [GRCh38]
Chr16:29920934..31450018 [GRCh37]
Chr16:29828435..31357519 [NCBI36]
Chr16:16p11.2		 pathogenic
GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3 copy number gain See cases [RCV000141141] Chr16:23752047..31943755 [GRCh38]
Chr16:23763368..31955076 [GRCh37]
Chr16:23670869..31862577 [NCBI36]
Chr16:16p12.2-11.2		 pathogenic
GRCh37/hg19 16p11.2(chr16:31154186-31926800)x3 copy number gain Breast ductal adenocarcinoma [RCV000207245] Chr16:31154186..31926800 [GRCh37]
Chr16:16p11.2		 uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3 copy number gain Breast ductal adenocarcinoma [RCV000207053] Chr16:1279324..31926800 [GRCh37]
Chr16:16p13.3-11.2		 uncertain significance
Single allele deletion Branched-chain keto acid dehydrogenase kinase deficiency [RCV000735205] Chr16:30554158..31536880 [GRCh37]
Chr16:16p11.2		 uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p11.2(chr16:30830287-31827011)x4 copy number gain See cases [RCV000447708] Chr16:30830287..31827011 [GRCh37]
Chr16:16p11.2		 uncertain significance
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 copy number gain See cases [RCV000511622] Chr16:9273328..89548493 [GRCh37]
Chr16:16p13.2-q24.3		 uncertain significance
GRCh37/hg19 16p11.2(chr16:28826162-29043901)x1 copy number loss See cases [RCV000448084] Chr16:28826162..29043901 [GRCh37]
Chr16:16p11.2		 likely pathogenic
maternal UPD(16p) complex Hemimegalencephaly [RCV000494707] Chr16:1280042..33710558 [GRCh37]
Chr16:16p13.3-11.2		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
NM_001136509.3(ZNF843):c.43G>A (p.Ala15Thr) single nucleotide variant not specified [RCV004320248] Chr16:31436807 [GRCh38]
Chr16:31448128 [GRCh37]
Chr16:16p11.2		 uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p11.2(chr16:30738551-34194635)x3 copy number gain not provided [RCV000739123] Chr16:30738551..34194635 [GRCh37]
Chr16:16p11.2		 benign
NM_001136509.3(ZNF843):c.776C>T (p.Pro259Leu) single nucleotide variant not specified [RCV004298423] Chr16:31436074 [GRCh38]
Chr16:31447395 [GRCh37]
Chr16:16p11.2		 uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-11.2(chr16:5805001-34230001) copy number gain Microcephaly [RCV001252948] Chr16:5805001..34230001 [GRCh37]
Chr16:16p13.3-11.2		 pathogenic
GRCh37/hg19 16p11.2(chr16:30350747-31905898)x3 copy number gain not provided [RCV001258619] Chr16:30350747..31905898 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.248G>A (p.Ser83Asn) single nucleotide variant not specified [RCV004292134] Chr16:31436602 [GRCh38]
Chr16:31447923 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.557G>C (p.Ser186Thr) single nucleotide variant not specified [RCV004161228] Chr16:31436293 [GRCh38]
Chr16:31447614 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.970C>G (p.Pro324Ala) single nucleotide variant not specified [RCV004119762] Chr16:31435880 [GRCh38]
Chr16:31447201 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.896G>C (p.Arg299Thr) single nucleotide variant not specified [RCV004216986] Chr16:31435954 [GRCh38]
Chr16:31447275 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.724G>A (p.Ala242Thr) single nucleotide variant not specified [RCV004190623] Chr16:31436126 [GRCh38]
Chr16:31447447 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.650G>A (p.Arg217Gln) single nucleotide variant not specified [RCV004247048] Chr16:31436200 [GRCh38]
Chr16:31447521 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.625C>G (p.Leu209Val) single nucleotide variant not specified [RCV004117195] Chr16:31436225 [GRCh38]
Chr16:31447546 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.661C>T (p.Leu221Phe) single nucleotide variant not specified [RCV004232886] Chr16:31436189 [GRCh38]
Chr16:31447510 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.538A>G (p.Ser180Gly) single nucleotide variant not specified [RCV004141801] Chr16:31436312 [GRCh38]
Chr16:31447633 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.829C>T (p.Arg277Trp) single nucleotide variant not specified [RCV004237218] Chr16:31436021 [GRCh38]
Chr16:31447342 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.532G>A (p.Val178Met) single nucleotide variant not specified [RCV004232391] Chr16:31436318 [GRCh38]
Chr16:31447639 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.537G>C (p.Glu179Asp) single nucleotide variant not specified [RCV004199202] Chr16:31436313 [GRCh38]
Chr16:31447634 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.490G>A (p.Val164Ile) single nucleotide variant not specified [RCV004109385] Chr16:31436360 [GRCh38]
Chr16:31447681 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.757G>T (p.Val253Phe) single nucleotide variant not specified [RCV004173226] Chr16:31436093 [GRCh38]
Chr16:31447414 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.120G>C (p.Arg40Ser) single nucleotide variant not specified [RCV004163403] Chr16:31436730 [GRCh38]
Chr16:31448051 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.319A>T (p.Thr107Ser) single nucleotide variant not specified [RCV004188917] Chr16:31436531 [GRCh38]
Chr16:31447852 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.1031A>G (p.Asn344Ser) single nucleotide variant not specified [RCV004261700] Chr16:31435819 [GRCh38]
Chr16:31447140 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.913G>T (p.Gly305Cys) single nucleotide variant not specified [RCV004248210] Chr16:31435937 [GRCh38]
Chr16:31447258 [GRCh37]
Chr16:16p11.2		 likely benign
NM_001136509.3(ZNF843):c.949G>T (p.Ala317Ser) single nucleotide variant not specified [RCV004272501] Chr16:31435901 [GRCh38]
Chr16:31447222 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.370G>A (p.Gly124Ser) single nucleotide variant not specified [RCV004269828] Chr16:31436480 [GRCh38]
Chr16:31447801 [GRCh37]
Chr16:16p11.2		 likely benign
GRCh37/hg19 16p11.2(chr16:31451337-31491435)x1 copy number loss not specified [RCV003987152] Chr16:31451337..31491435 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.284G>A (p.Arg95Gln) single nucleotide variant not specified [RCV004495133] Chr16:31436566 [GRCh38]
Chr16:31447887 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.417C>A (p.His139Gln) single nucleotide variant not specified [RCV004495134] Chr16:31436433 [GRCh38]
Chr16:31447754 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.682A>T (p.Ser228Cys) single nucleotide variant not specified [RCV004495135] Chr16:31436168 [GRCh38]
Chr16:31447489 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.797C>T (p.Ala266Val) single nucleotide variant not specified [RCV004495136] Chr16:31436053 [GRCh38]
Chr16:31447374 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.893A>G (p.His298Arg) single nucleotide variant not specified [RCV004495140] Chr16:31435957 [GRCh38]
Chr16:31447278 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.176G>A (p.Arg59Gln) single nucleotide variant not specified [RCV004335552] Chr16:31436674 [GRCh38]
Chr16:31447995 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.977G>T (p.Trp326Leu) single nucleotide variant not specified [RCV004336536] Chr16:31435873 [GRCh38]
Chr16:31447194 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.805C>T (p.Pro269Ser) single nucleotide variant not specified [RCV004495137] Chr16:31436045 [GRCh38]
Chr16:31447366 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.809G>A (p.Arg270Lys) single nucleotide variant not specified [RCV004495138] Chr16:31436041 [GRCh38]
Chr16:31447362 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_001136509.3(ZNF843):c.883G>C (p.Ala295Pro) single nucleotide variant not specified [RCV004495139] Chr16:31435967 [GRCh38]
Chr16:31447288 [GRCh37]
Chr16:16p11.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:524
Count of miRNA genes:440
Interacting mature miRNAs:460
Transcripts:ENST00000315678, ENST00000564218
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
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
sY3084  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map4q27UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map1p35.3-p33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q32.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map3q12.3UniSTS


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 1 1
Low 1221 1715 1122 138 168 55 3722 1508 3458 237 1263 1087 87 874 2442 1
Below cutoff 1201 1195 585 468 1566 393 631 685 249 177 180 517 83 330 346 3

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000315678   ⟹   ENSP00000322899
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,435,434 - 31,442,789 (-)Ensembl
RefSeq Acc Id: ENST00000564218   ⟹   ENSP00000455858
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,432,593 - 31,443,025 (-)Ensembl
RefSeq Acc Id: ENST00000618063   ⟹   ENSP00000483573
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,435,438 - 31,443,160 (-)Ensembl
RefSeq Acc Id: NM_001136509   ⟹   NP_001129981
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,435,434 - 31,442,789 (-)NCBI
GRCh371631,446,885 - 31,454,348 (-)RGD
Celera1628,854,038 - 28,861,497 (+)RGD
HuRef1629,007,272 - 29,014,730 (-)RGD
CHM1_11632,765,512 - 32,772,971 (-)NCBI
T2T-CHM13v2.01631,822,848 - 31,830,198 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001353381   ⟹   NP_001340310
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,435,438 - 31,443,160 (-)NCBI
T2T-CHM13v2.01631,822,852 - 31,830,569 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_001129981   ⟸   NM_001136509
- UniProtKB: A8K4U8 (UniProtKB/Swiss-Prot),   Q8N446 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001340310   ⟸   NM_001353381
- UniProtKB: Q8N446 (UniProtKB/Swiss-Prot),   A8K4U8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000455858   ⟸   ENST00000564218
RefSeq Acc Id: ENSP00000483573   ⟸   ENST00000618063
RefSeq Acc Id: ENSP00000322899   ⟸   ENST00000315678
Protein Domains
C2H2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8N446-F1-model_v2 AlphaFold Q8N446 1-348 view protein structure

Promoters
RGD ID:6793649
Promoter ID:HG_KWN:23629
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000315678,   UC002EBY.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361631,361,611 - 31,362,111 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
COSMIC ZNF843 COSMIC
Ensembl Genes ENSG00000176723 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000315678 ENTREZGENE
  ENST00000315678.10 UniProtKB/Swiss-Prot
  ENST00000564218.5 UniProtKB/TrEMBL
  ENST00000618063 ENTREZGENE
  ENST00000618063.1 UniProtKB/Swiss-Prot
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000176723 GTEx
HGNC ID HGNC:28710 ENTREZGENE
Human Proteome Map ZNF843 Human Proteome Map
InterPro Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:283933 UniProtKB/Swiss-Prot
NCBI Gene 283933 ENTREZGENE
PANTHER LMO7 DOWNSTREAM NEIGHBOR PROTEIN UniProtKB/TrEMBL
  PRIMATE-EXPANDED PROTEIN FAMILY UniProtKB/TrEMBL
PharmGKB PA162410853 PharmGKB
PRINTS F138DOMAIN UniProtKB/TrEMBL
PROSITE ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K4U8 ENTREZGENE
  H3BQN5_HUMAN UniProtKB/TrEMBL
  Q8N446 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A8K4U8 UniProtKB/Swiss-Prot