ZNF134 (zinc finger protein 134) - Rat Genome Database

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Gene: ZNF134 (zinc finger protein 134) Homo sapiens
Analyze
Symbol: ZNF134
Name: zinc finger protein 134
RGD ID: 1352509
HGNC Page HGNC:12918
Description: Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Predicted to be located in nucleus. Predicted to be active in nucleoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: MGC138499; MGC141970; pHZ-15; zinc finger protein 134 (clone pHZ-15)
RGD Orthologs
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: LOC100419834  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381957,614,242 - 57,624,724 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1957,614,233 - 57,624,724 (+)EnsemblGRCh38hg38GRCh38
GRCh371958,125,610 - 58,136,092 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361962,817,642 - 62,825,448 (+)NCBINCBI36Build 36hg18NCBI36
Build 341962,817,439 - 62,826,533NCBI
Celera1955,169,407 - 55,177,213 (+)NCBICelera
Cytogenetic Map19q13.43NCBI
HuRef1954,438,256 - 54,446,062 (+)NCBIHuRef
CHM1_11958,119,534 - 58,127,952 (+)NCBICHM1_1
T2T-CHM13v2.01960,711,171 - 60,721,651 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Biological Process

Cellular Component
nucleoplasm  (IBA)
nucleus  (IEA)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7557990   PMID:12477932   PMID:16344560   PMID:18029348   PMID:21873635   PMID:25144775   PMID:32296183  


Genomics

Comparative Map Data
ZNF134
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381957,614,242 - 57,624,724 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1957,614,233 - 57,624,724 (+)EnsemblGRCh38hg38GRCh38
GRCh371958,125,610 - 58,136,092 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361962,817,642 - 62,825,448 (+)NCBINCBI36Build 36hg18NCBI36
Build 341962,817,439 - 62,826,533NCBI
Celera1955,169,407 - 55,177,213 (+)NCBICelera
Cytogenetic Map19q13.43NCBI
HuRef1954,438,256 - 54,446,062 (+)NCBIHuRef
CHM1_11958,119,534 - 58,127,952 (+)NCBICHM1_1
T2T-CHM13v2.01960,711,171 - 60,721,651 (+)NCBIT2T-CHM13v2.0
ZNF134
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22063,893,788 - 63,904,603 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11965,680,309 - 65,692,131 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01954,626,116 - 54,636,580 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1 Ensembl1963,460,448 - 63,462,383 (+)Ensemblpanpan1.1panPan2
LOC119870876
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ROS_Cfam_1.01100,990,704 - 100,997,660 (+)NCBIROS_Cfam_1.0
UMICH_Zoey_3.11100,659,823 - 100,666,778 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01100,346,726 - 100,353,680 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01101,102,394 - 101,109,350 (+)NCBIUU_Cfam_GSD_1.0
Znf134
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409349263,188 - 266,413 (-)NCBIHiC_Itri_2
SpeTri2.0NW_004936897440,218 - 443,537 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF134
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1662,082,810 - 62,121,795 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2656,711,977 - 56,720,051 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ZNF134
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1649,987,989 - 49,995,590 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl649,987,988 - 49,995,064 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660453,239,891 - 3,250,557 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Znf134
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473312,854,729 - 12,856,731 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZNF134
30 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
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 19q13.43(chr19:56363208-58581203)x3 copy number gain See cases [RCV000052927] Chr19:56363208..58581203 [GRCh38]
Chr19:56874577..59092570 [GRCh37]
Chr19:61566389..63784382 [NCBI36]
Chr19:19q13.43		 pathogenic
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(chr19:47908540-58539965)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
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(chr19:52955056-58581203)x3 copy number gain See cases [RCV000134139] Chr19:52955056..58581203 [GRCh38]
Chr19:53458309..59092570 [GRCh37]
Chr19:58150121..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3 copy number gain See cases [RCV000134174] Chr19:52612432..58581203 [GRCh38]
Chr19:53115685..59092570 [GRCh37]
Chr19:57807497..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.43(chr19:57546443-57889946)x3 copy number gain See cases [RCV000141360] Chr19:57546443..57889946 [GRCh38]
Chr19:58057811..58401314 [GRCh37]
Chr19:62749623..63093126 [NCBI36]
Chr19:19q13.43		 uncertain significance
GRCh38/hg38 19q13.43(chr19:56353449-58445521)x3 copy number gain See cases [RCV000141900] Chr19:56353449..58445521 [GRCh38]
Chr19:56864818..58956888 [GRCh37]
Chr19:61556630..63648700 [NCBI36]
Chr19:19q13.43		 uncertain significance
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 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:50489390..59095359 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.43(chr19:58133156-58153681)x3 copy number gain See cases [RCV000446579] Chr19:58133156..58153681 [GRCh37]
Chr19:19q13.43		 likely benign
GRCh37/hg19 19q13.42-13.43(chr19:54344821-58956888)x3 copy number gain See cases [RCV000448186] Chr19:54344821..58956888 [GRCh37]
Chr19:19q13.42-13.43		 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 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 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 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 19q13.43(chr19:58026984-58246176)x1 copy number loss See cases [RCV000512135] Chr19:58026984..58246176 [GRCh37]
Chr19:19q13.43		 uncertain significance
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
GRCh37/hg19 19q13.43(chr19:56706500-58956888)x3 copy number gain See cases [RCV000512396] Chr19:56706500..58956888 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3 copy number gain not provided [RCV000684095] Chr19:54196216..58759679 [GRCh37]
Chr19:19q13.42-13.43		 pathogenic
Single allele duplication not provided [RCV000677936] Chr19:57953199..58196644 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.43(chr19:57891243-58536930)x3 copy number gain not provided [RCV000684084] Chr19:57891243..58536930 [GRCh37]
Chr19:19q13.43		 likely benign
GRCh37/hg19 19q13.43(chr19:58092045-58686148)x3 copy number gain not provided [RCV000849080] Chr19:58092045..58686148 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.43(chr19:57952073-58661581)x3 copy number gain not provided [RCV000846105] Chr19:57952073..58661581 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.43(chr19:58054819-58410552)x3 copy number gain not provided [RCV000848932] Chr19:58054819..58410552 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.43(chr19:58026985-58255427)x3 copy number gain not provided [RCV001832942] Chr19:58026985..58255427 [GRCh37]
Chr19:19q13.43		 likely benign
NM_003435.5(ZNF134):c.769G>C (p.Glu257Gln) single nucleotide variant not specified [RCV004215129] Chr19:57620888 [GRCh38]
Chr19:58132256 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.856A>T (p.Arg286Trp) single nucleotide variant not specified [RCV004196031] Chr19:57620975 [GRCh38]
Chr19:58132343 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.182A>T (p.Asp61Val) single nucleotide variant not specified [RCV004215075] Chr19:57620301 [GRCh38]
Chr19:58131669 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.689G>A (p.Arg230Lys) single nucleotide variant not specified [RCV004215076] Chr19:57620808 [GRCh38]
Chr19:58132176 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.428C>G (p.Ala143Gly) single nucleotide variant not specified [RCV004200188] Chr19:57620547 [GRCh38]
Chr19:58131915 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.1078A>G (p.Ile360Val) single nucleotide variant not specified [RCV004088376] Chr19:57621197 [GRCh38]
Chr19:58132565 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.559C>T (p.Arg187Cys) single nucleotide variant not specified [RCV004188914] Chr19:57620678 [GRCh38]
Chr19:58132046 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.520A>G (p.Met174Val) single nucleotide variant not specified [RCV004180990] Chr19:57620639 [GRCh38]
Chr19:58132007 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.325G>A (p.Asp109Asn) single nucleotide variant not specified [RCV004239786] Chr19:57620444 [GRCh38]
Chr19:58131812 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.143C>T (p.Thr48Met) single nucleotide variant not specified [RCV004174141] Chr19:57620262 [GRCh38]
Chr19:58131630 [GRCh37]
Chr19:19q13.43		 likely benign
NM_003435.5(ZNF134):c.646A>G (p.Lys216Glu) single nucleotide variant not specified [RCV004077494] Chr19:57620765 [GRCh38]
Chr19:58132133 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.100G>C (p.Val34Leu) single nucleotide variant not specified [RCV004199201] Chr19:57620219 [GRCh38]
Chr19:58131587 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.208G>T (p.Gly70Cys) single nucleotide variant not specified [RCV004122371] Chr19:57620327 [GRCh38]
Chr19:58131695 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.797G>A (p.Gly266Glu) single nucleotide variant not specified [RCV004093546] Chr19:57620916 [GRCh38]
Chr19:58132284 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.182A>G (p.Asp61Gly) single nucleotide variant not specified [RCV004219074] Chr19:57620301 [GRCh38]
Chr19:58131669 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.398C>T (p.Thr133Met) single nucleotide variant not specified [RCV004194121] Chr19:57620517 [GRCh38]
Chr19:58131885 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.1103G>T (p.Gly368Val) single nucleotide variant not specified [RCV004263539] Chr19:57621222 [GRCh38]
Chr19:58132590 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.653C>T (p.Thr218Ile) single nucleotide variant not specified [RCV004302477] Chr19:57620772 [GRCh38]
Chr19:58132140 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.644G>A (p.Arg215His) single nucleotide variant not specified [RCV004284351] Chr19:57620763 [GRCh38]
Chr19:58132131 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.478C>T (p.His160Tyr) single nucleotide variant not specified [RCV004288891] Chr19:57620597 [GRCh38]
Chr19:58131965 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.809G>C (p.Ser270Thr) single nucleotide variant not specified [RCV004278041] Chr19:57620928 [GRCh38]
Chr19:58132296 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.278T>G (p.Leu93Arg) single nucleotide variant not specified [RCV004282887] Chr19:57620397 [GRCh38]
Chr19:58131765 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.172A>G (p.Ile58Val) single nucleotide variant not specified [RCV004323952] Chr19:57620291 [GRCh38]
Chr19:58131659 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.1279C>T (p.Leu427Phe) single nucleotide variant not specified [RCV004292180] Chr19:57621398 [GRCh38]
Chr19:58132766 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.1123A>G (p.Ser375Gly) single nucleotide variant not specified [RCV004338472] Chr19:57621242 [GRCh38]
Chr19:58132610 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.1151C>T (p.Thr384Ile) single nucleotide variant not specified [RCV004297380] Chr19:57621270 [GRCh38]
Chr19:58132638 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.1047C>T (p.Cys349=) single nucleotide variant not provided [RCV003425459] Chr19:57621166 [GRCh38]
Chr19:58132534 [GRCh37]
Chr19:19q13.43		 likely benign
NM_003435.5(ZNF134):c.197A>C (p.Asp66Ala) single nucleotide variant not specified [RCV004352234] Chr19:57620316 [GRCh38]
Chr19:58131684 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.43(chr19:58034484-58421498)x3 copy number gain not provided [RCV003485203] Chr19:58034484..58421498 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.40+93A>C single nucleotide variant not provided [RCV003415475] Chr19:57619601 [GRCh38]
Chr19:58130969 [GRCh37]
Chr19:19q13.43		 likely benign
NM_003435.5(ZNF134):c.497G>T (p.Gly166Val) single nucleotide variant not specified [RCV004489308] Chr19:57620616 [GRCh38]
Chr19:58131984 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.1048G>A (p.Gly350Arg) single nucleotide variant not specified [RCV004489304] Chr19:57621167 [GRCh38]
Chr19:58132535 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.268A>G (p.Ser90Gly) single nucleotide variant not specified [RCV004489305] Chr19:57620387 [GRCh38]
Chr19:58131755 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.326A>G (p.Asp109Gly) single nucleotide variant not specified [RCV004489306] Chr19:57620445 [GRCh38]
Chr19:58131813 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_003435.5(ZNF134):c.483G>T (p.Arg161Ser) single nucleotide variant not specified [RCV004489307] Chr19:57620602 [GRCh38]
Chr19:58131970 [GRCh37]
Chr19:19q13.43		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1308
Count of miRNA genes:840
Interacting mature miRNAs:973
Transcripts:ENST00000396161, ENST00000597975, ENST00000600344, ENST00000600883
Prediction methods:Microtar, 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
STS-U09412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371958,132,822 - 58,132,942UniSTSGRCh37
Build 361962,824,634 - 62,824,754RGDNCBI36
Celera1955,176,399 - 55,176,519RGD
Cytogenetic Map19q13.4UniSTS
HuRef1954,445,248 - 54,445,368UniSTS
GeneMap99-GB4 RH Map19287.74UniSTS
NCBI RH Map19600.5UniSTS
D19S1016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371958,133,122 - 58,133,240UniSTSGRCh37
Build 361962,824,934 - 62,825,052RGDNCBI36
Celera1955,176,699 - 55,176,817RGD
Cytogenetic Map19q13.4UniSTS
HuRef1954,445,548 - 54,445,666UniSTS


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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1052 409 809 65 847 48 1761 623 1113 186 822 1012 29 1 167 998 3 2
Low 1341 2552 916 558 1071 416 2595 1572 2620 231 627 596 146 1037 1790 2
Below cutoff 8 30 1 1 29 1 2 1 2 4 2

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000396161   ⟹   ENSP00000379464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1957,614,242 - 57,624,724 (+)Ensembl
RefSeq Acc Id: ENST00000597975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1957,614,233 - 57,620,447 (+)Ensembl
RefSeq Acc Id: ENST00000600344   ⟹   ENSP00000472314
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1957,614,238 - 57,619,628 (+)Ensembl
RefSeq Acc Id: ENST00000600883   ⟹   ENSP00000469065
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1957,614,256 - 57,620,318 (+)Ensembl
RefSeq Acc Id: NM_003435   ⟹   NP_003426
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381957,614,242 - 57,624,724 (+)NCBI
GRCh371958,125,830 - 58,133,636 (+)RGD
Build 361962,817,642 - 62,825,448 (+)NCBI Archive
Celera1955,169,407 - 55,177,213 (+)RGD
HuRef1954,438,256 - 54,446,062 (+)ENTREZGENE
CHM1_11958,119,534 - 58,130,030 (+)NCBI
T2T-CHM13v2.01960,711,171 - 60,721,651 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_003426   ⟸   NM_003435
- UniProtKB: Q9Y4B2 (UniProtKB/Swiss-Prot),   P52741 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000472314   ⟸   ENST00000600344
RefSeq Acc Id: ENSP00000469065   ⟸   ENST00000600883
RefSeq Acc Id: ENSP00000379464   ⟸   ENST00000396161
Protein Domains
C2H2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P52741-F1-model_v2 AlphaFold P52741 1-427 view protein structure

Promoters
RGD ID:13205913
Promoter ID:EPDNEW_H26537
Type:initiation region
Name:ZNF134_1
Description:zinc finger protein 134
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381957,614,242 - 57,614,302EPDNEW
RGD ID:6796255
Promoter ID:HG_KWN:31176
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_003435,   UC002QPO.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361962,817,184 - 62,817,684 (+)MPROMDB
RGD ID:6851648
Promoter ID:EP73626
Type:multiple initiation site
Name:HS_ZNF134
Description:Zinc finger protein 134 (clone pHZ-15).
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:NEDO full length human cDNA sequencing project.; Oligo-capping
Position:
Human AssemblyChrPosition (strand)Source
Build 361962,817,431 - 62,817,491EPD

Additional Information

Database Acc Id Source(s)
COSMIC ZNF134 COSMIC
Ensembl Genes ENSG00000213762 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000396161 ENTREZGENE
  ENST00000396161.10 UniProtKB/Swiss-Prot
  ENST00000600344.1 UniProtKB/TrEMBL
  ENST00000600883.1 UniProtKB/TrEMBL
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000213762 GTEx
HGNC ID HGNC:12918 ENTREZGENE
Human Proteome Map ZNF134 Human Proteome Map
InterPro Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:7693 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 7693 ENTREZGENE
OMIM 604076 OMIM
PANTHER KRAB DOMAIN C2H2 ZINC FINGER UniProtKB/TrEMBL
  KRAB DOMAIN-CONTAINING PROTEIN 5-RELATED UniProtKB/TrEMBL
  ZINC FINGER AND BTB DOMAIN-CONTAINING PROTEIN 17 UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN 142 UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN 726 UniProtKB/TrEMBL
Pfam zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37506 PharmGKB
PROSITE ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt M0QXC7_HUMAN UniProtKB/TrEMBL
  M0R246_HUMAN UniProtKB/TrEMBL
  P52741 ENTREZGENE
  Q5U5N5_HUMAN UniProtKB/TrEMBL
  Q6PJ68_HUMAN UniProtKB/TrEMBL
  Q6PJU4_HUMAN UniProtKB/TrEMBL
  Q9Y4B2 ENTREZGENE
  ZN134_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q9Y4B2 UniProtKB/Swiss-Prot