ZNF382 (zinc finger protein 382) - Rat Genome Database

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Gene: ZNF382 (zinc finger protein 382) Homo sapiens
Analyze
Symbol: ZNF382
Name: zinc finger protein 382
RGD ID: 1352355
HGNC Page HGNC:17409
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. Predicted to be located in nucleus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ14686; KRAB/zinc finger suppressor protein 1; KS1; multiple zinc finger and krueppel-associated box protein KS1; multiple-zinc-finger-Kruppel-associated box protein KS1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
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
GRCh381936,605,313 - 36,634,114 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1936,604,817 - 36,634,114 (+)EnsemblGRCh38hg38GRCh38
GRCh371937,096,215 - 37,125,016 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361941,788,061 - 41,811,339 (+)NCBINCBI36Build 36hg18NCBI36
Build 341941,788,060 - 41,811,338NCBI
Celera1933,880,792 - 33,904,099 (+)NCBICelera
Cytogenetic Map19q13.12NCBI
HuRef1933,564,157 - 33,587,507 (+)NCBIHuRef
CHM1_11937,096,795 - 37,120,088 (+)NCBICHM1_1
T2T-CHM13v2.01939,280,598 - 39,309,416 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
nucleus  (IEA)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Large-scale characterization of DNA methylation changes in human gastric carcinomas with and without metastasis. Liu Z, etal., Clin Cancer Res. 2014 Sep 1;20(17):4598-612. doi: 10.1158/1078-0432.CCR-13-3380. Epub 2014 Jul 9.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9835615   PMID:11154279   PMID:12459182   PMID:12477932   PMID:14519192   PMID:14702039   PMID:20682794   PMID:21873635   PMID:21876767   PMID:25319049   PMID:25820252   PMID:29760376  
PMID:29956735   PMID:30804458   PMID:31678273   PMID:33150179   PMID:33961781  


Genomics

Comparative Map Data
ZNF382
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381936,605,313 - 36,634,114 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1936,604,817 - 36,634,114 (+)EnsemblGRCh38hg38GRCh38
GRCh371937,096,215 - 37,125,016 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361941,788,061 - 41,811,339 (+)NCBINCBI36Build 36hg18NCBI36
Build 341941,788,060 - 41,811,338NCBI
Celera1933,880,792 - 33,904,099 (+)NCBICelera
Cytogenetic Map19q13.12NCBI
HuRef1933,564,157 - 33,587,507 (+)NCBIHuRef
CHM1_11937,096,795 - 37,120,088 (+)NCBICHM1_1
T2T-CHM13v2.01939,280,598 - 39,309,416 (+)NCBIT2T-CHM13v2.0
Zfp382
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39729,821,255 - 29,840,180 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl729,821,367 - 29,834,375 (+)EnsemblGRCm39 Ensembl
GRCm38730,121,833 - 30,140,758 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl730,121,942 - 30,134,950 (+)EnsemblGRCm38mm10GRCm38
MGSCv37730,906,967 - 30,920,051 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36729,830,708 - 29,843,792 (+)NCBIMGSCv36mm8
Celera724,724,357 - 24,738,559 (+)NCBICelera
Cytogenetic Map7B1NCBI
Zfp382
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8194,504,344 - 94,528,316 (+)NCBIGRCr8
mRatBN7.2185,377,614 - 85,400,832 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl185,377,484 - 85,399,667 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx190,795,435 - 90,818,893 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0199,264,250 - 99,287,453 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0192,553,703 - 92,577,163 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0188,582,641 - 88,603,219 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl188,581,206 - 88,605,697 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0189,743,564 - 89,763,846 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4185,175,213 - 85,184,576 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1185,253,323 - 85,262,683 (+)NCBI
Celera179,753,982 - 79,774,540 (+)NCBICelera
Cytogenetic Map1q21NCBI
Znf382
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554682,278,594 - 2,299,493 (+)NCBIChiLan1.0ChiLan1.0
ZNF382
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22042,747,013 - 42,775,910 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11944,631,787 - 44,660,680 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01933,566,071 - 33,594,961 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11943,176,836 - 43,199,770 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1943,176,591 - 43,199,760 (-)Ensemblpanpan1.1panPan2
ZNF382
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11116,226,916 - 116,278,163 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1116,252,743 - 116,277,633 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1115,633,164 - 115,684,983 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01116,828,932 - 116,880,949 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1116,829,615 - 116,880,948 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11116,398,704 - 116,450,707 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01116,017,627 - 116,069,916 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01117,069,239 - 117,121,249 (+)NCBIUU_Cfam_GSD_1.0
Znf382
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934911,571,859 - 11,594,975 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936922347,898 - 362,345 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936922348,997 - 362,345 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF382
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl645,777,393 - 45,812,338 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1645,776,183 - 45,795,964 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2641,220,163 - 41,236,080 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ZNF382
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1631,429,216 - 31,482,534 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660739,233,325 - 9,288,334 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Znf382
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462479410,573,286 - 10,590,943 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462479410,577,110 - 10,646,192 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZNF382
18 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.12(chr19:36439647-37163160)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051288]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051288]|See cases [RCV000051288] Chr19:36439647..37163160 [GRCh38]
Chr19:36930549..37654062 [GRCh37]
Chr19:41622389..42345902 [NCBI36]
Chr19:19q13.12		 uncertain significance
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1 copy number loss See cases [RCV000135879] Chr19:29661858..38114723 [GRCh38]
Chr19:30152765..38605363 [GRCh37]
Chr19:34844605..43297203 [NCBI36]
Chr19:19q12-13.13		 pathogenic
GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1 copy number loss See cases [RCV000136794] Chr19:29671324..37902990 [GRCh38]
Chr19:30162231..38393630 [GRCh37]
Chr19:34854071..43085470 [NCBI36]
Chr19:19q12-13.13		 pathogenic
GRCh37/hg19 19q13.12-13.2(chr19:36685995-38708166)x1 copy number loss Breast ductal adenocarcinoma [RCV000207200] Chr19:36685995..38708166 [GRCh37]
Chr19:19q13.12-13.2		 uncertain significance
chr19:36674305-38652962 complex variant complex Breast ductal adenocarcinoma [RCV000207036] Chr19:36674305..38652962 [GRCh37]
Chr19:19q13.12-13.13		 uncertain significance
GRCh37/hg19 19q13.12-13.13(chr19:36475577-38399402)x3 copy number gain See cases [RCV000240597] Chr19:36475577..38399402 [GRCh37]
Chr19:19q13.12-13.13		 uncertain significance
GRCh37/hg19 19q13.12(chr19:36910874-37705345)x1 copy number loss See cases [RCV000447259] Chr19:36910874..37705345 [GRCh37]
Chr19:19q13.12		 uncertain significance
GRCh37/hg19 19q13.12(chr19:36147111-37249653)x1 copy number loss See cases [RCV000511504] Chr19:36147111..37249653 [GRCh37]
Chr19:19q13.12		 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 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_032825.5(ZNF382):c.163A>G (p.Met55Val) single nucleotide variant not specified [RCV004310151] Chr19:36610673 [GRCh38]
Chr19:37101575 [GRCh37]
Chr19:19q13.12		 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 19q13.11-13.12(chr19:35111811-37744992) copy number loss Generalized epilepsy with febrile seizures plus, type 1 [RCV000767768] Chr19:35111811..37744992 [GRCh37]
Chr19:19q13.11-13.12		 pathogenic
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3 copy number gain not provided [RCV000845733] Chr19:28271106..49213832 [GRCh37]
Chr19:19q11-13.33		 pathogenic
GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3 copy number gain Specific learning disability [RCV001801194] Chr19:19546923..41313229 [GRCh37]
Chr19:19p13.11-q13.2		 pathogenic
GRCh37/hg19 19q13.12(chr19:36910874-37705345) copy number loss not specified [RCV002052681] Chr19:36910874..37705345 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1643G>A (p.Gly548Glu) single nucleotide variant not specified [RCV004328589] Chr19:36627540 [GRCh38]
Chr19:37118442 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.75C>A (p.Asp25Glu) single nucleotide variant not specified [RCV004233177] Chr19:36609989 [GRCh38]
Chr19:37100891 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.214C>G (p.Pro72Ala) single nucleotide variant not specified [RCV004164272] Chr19:36610724 [GRCh38]
Chr19:37101626 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1483C>G (p.Pro495Ala) single nucleotide variant not specified [RCV004110761] Chr19:36627380 [GRCh38]
Chr19:37118282 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.934A>G (p.Ile312Val) single nucleotide variant not specified [RCV004200383] Chr19:36626831 [GRCh38]
Chr19:37117733 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.336G>C (p.Glu112Asp) single nucleotide variant not specified [RCV004095351] Chr19:36626233 [GRCh38]
Chr19:37117135 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1329G>T (p.Lys443Asn) single nucleotide variant not specified [RCV004160047] Chr19:36627226 [GRCh38]
Chr19:37118128 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.860A>C (p.Gln287Pro) single nucleotide variant not specified [RCV004170254] Chr19:36626757 [GRCh38]
Chr19:37117659 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1084C>T (p.Arg362Cys) single nucleotide variant not specified [RCV004127500] Chr19:36626981 [GRCh38]
Chr19:37117883 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.164T>G (p.Met55Arg) single nucleotide variant not specified [RCV004148331] Chr19:36610674 [GRCh38]
Chr19:37101576 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.254A>G (p.Asp85Gly) single nucleotide variant not specified [RCV004122256] Chr19:36626151 [GRCh38]
Chr19:37117053 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1600A>G (p.Asn534Asp) single nucleotide variant not specified [RCV004131938] Chr19:36627497 [GRCh38]
Chr19:37118399 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.785T>C (p.Leu262Pro) single nucleotide variant not specified [RCV004078664] Chr19:36626682 [GRCh38]
Chr19:37117584 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.170G>A (p.Arg57His) single nucleotide variant not specified [RCV004258340] Chr19:36610680 [GRCh38]
Chr19:37101582 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1420C>T (p.Arg474Cys) single nucleotide variant not specified [RCV004255586] Chr19:36627317 [GRCh38]
Chr19:37118219 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.663C>G (p.Phe221Leu) single nucleotide variant not specified [RCV004272403] Chr19:36626560 [GRCh38]
Chr19:37117462 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1475A>G (p.Asn492Ser) single nucleotide variant not specified [RCV004314281] Chr19:36627372 [GRCh38]
Chr19:37118274 [GRCh37]
Chr19:19q13.12		 uncertain significance
GRCh37/hg19 19q13.12(chr19:36804753-37720742)x1 copy number loss not provided [RCV003483353] Chr19:36804753..37720742 [GRCh37]
Chr19:19q13.12		 uncertain significance
Single allele deletion not provided [RCV003448708] Chr19:35225414..37357598 [GRCh37]
Chr19:19q13.11-13.12		 pathogenic
GRCh37/hg19 19q11-13.2(chr19:28271146-41508851)x3 copy number gain not specified [RCV003986115] Chr19:28271146..41508851 [GRCh37]
Chr19:19q11-13.2		 pathogenic
NM_032825.5(ZNF382):c.1610T>C (p.Val537Ala) single nucleotide variant not specified [RCV004486766] Chr19:36627507 [GRCh38]
Chr19:37118409 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.238G>T (p.Asp80Tyr) single nucleotide variant not specified [RCV004486767] Chr19:36626135 [GRCh38]
Chr19:37117037 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.487G>A (p.Asp163Asn) single nucleotide variant not specified [RCV004486768] Chr19:36626384 [GRCh38]
Chr19:37117286 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1508G>A (p.Arg503Lys) single nucleotide variant not specified [RCV004486765] Chr19:36627405 [GRCh38]
Chr19:37118307 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.851T>C (p.Ile284Thr) single nucleotide variant not specified [RCV004486770] Chr19:36626748 [GRCh38]
Chr19:37117650 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.737G>A (p.Gly246Glu) single nucleotide variant not specified [RCV004486769] Chr19:36626634 [GRCh38]
Chr19:37117536 [GRCh37]
Chr19:19q13.12		 uncertain significance
NM_032825.5(ZNF382):c.1421G>A (p.Arg474His) single nucleotide variant not specified [RCV004486764] Chr19:36627318 [GRCh38]
Chr19:37118220 [GRCh37]
Chr19:19q13.12		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1615
Count of miRNA genes:663
Interacting mature miRNAs:721
Transcripts:ENST00000292928, ENST00000423582, ENST00000435416, ENST00000439428, ENST00000460384, ENST00000460670, ENST00000463910, ENST00000590785
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
SHGC-83924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371937,111,062 - 37,111,391UniSTSGRCh37
Build 361941,802,902 - 41,803,231RGDNCBI36
Celera1933,895,655 - 33,895,984RGD
Cytogenetic Map19q13.12UniSTS
HuRef1933,579,059 - 33,579,388UniSTS
TNG Radiation Hybrid Map1913248.0UniSTS
RH123256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371937,100,637 - 37,100,933UniSTSGRCh37
Build 361941,792,477 - 41,792,773RGDNCBI36
Celera1933,885,205 - 33,885,501RGD
Cytogenetic Map19q13.12UniSTS
HuRef1933,568,585 - 33,568,881UniSTS
TNG Radiation Hybrid Map1913259.0UniSTS


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 3 2 46 2 487 20 9 1
Low 1902 2107 1376 240 1037 129 2370 1354 3185 358 1342 1411 116 1 767 1544 5 2
Below cutoff 526 873 340 376 857 328 1986 840 62 60 96 192 57 437 1244 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000292928   ⟹   ENSP00000292928
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,605,313 - 36,634,114 (+)Ensembl
RefSeq Acc Id: ENST00000423582   ⟹   ENSP00000389722
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,604,817 - 36,627,992 (+)Ensembl
RefSeq Acc Id: ENST00000435416   ⟹   ENSP00000410113
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,608,420 - 36,628,270 (+)Ensembl
RefSeq Acc Id: ENST00000439428   ⟹   ENSP00000407593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,605,335 - 36,628,567 (+)Ensembl
RefSeq Acc Id: ENST00000460384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,605,313 - 36,608,092 (+)Ensembl
RefSeq Acc Id: ENST00000460670   ⟹   ENSP00000467675
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,605,313 - 36,609,993 (+)Ensembl
RefSeq Acc Id: ENST00000463910
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,605,328 - 36,607,811 (+)Ensembl
RefSeq Acc Id: ENST00000585467
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,628,793 - 36,630,190 (+)Ensembl
RefSeq Acc Id: ENST00000590785   ⟹   ENSP00000465485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,610,498 - 36,626,596 (+)Ensembl
RefSeq Acc Id: ENST00000639288   ⟹   ENSP00000492867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1936,626,774 - 36,628,842 (+)Ensembl
RefSeq Acc Id: NM_001256838   ⟹   NP_001243767
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,605,313 - 36,634,114 (+)NCBI
GRCh371937,096,207 - 37,119,499 (+)NCBI
HuRef1933,564,157 - 33,587,507 (+)NCBI
CHM1_11937,096,795 - 37,120,088 (+)NCBI
T2T-CHM13v2.01939,280,598 - 39,309,416 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001398490   ⟹   NP_001385419
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,605,313 - 36,634,114 (+)NCBI
T2T-CHM13v2.01939,280,598 - 39,309,416 (+)NCBI
RefSeq Acc Id: NM_001398491   ⟹   NP_001385420
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,605,313 - 36,634,114 (+)NCBI
T2T-CHM13v2.01939,280,598 - 39,309,416 (+)NCBI
RefSeq Acc Id: NM_001398492   ⟹   NP_001385421
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,605,313 - 36,634,114 (+)NCBI
T2T-CHM13v2.01939,280,598 - 39,309,416 (+)NCBI
RefSeq Acc Id: NM_032825   ⟹   NP_116214
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,605,313 - 36,634,114 (+)NCBI
GRCh371937,096,207 - 37,119,499 (+)NCBI
Build 361941,788,061 - 41,811,339 (+)NCBI Archive
Celera1933,880,792 - 33,904,099 (+)RGD
HuRef1933,564,157 - 33,587,507 (+)NCBI
CHM1_11937,096,795 - 37,120,088 (+)NCBI
T2T-CHM13v2.01939,280,598 - 39,309,416 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_116214   ⟸   NM_032825
- Peptide Label: isoform 1
- UniProtKB: Q53ZY8 (UniProtKB/Swiss-Prot),   C9K0V5 (UniProtKB/Swiss-Prot),   A8MT55 (UniProtKB/Swiss-Prot),   A3KMP6 (UniProtKB/Swiss-Prot),   Q5JPJ2 (UniProtKB/Swiss-Prot),   Q96SR6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001243767   ⟸   NM_001256838
- Peptide Label: isoform 2
- UniProtKB: Q96SR6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000389722   ⟸   ENST00000423582
RefSeq Acc Id: ENSP00000292928   ⟸   ENST00000292928
RefSeq Acc Id: ENSP00000407593   ⟸   ENST00000439428
RefSeq Acc Id: ENSP00000492867   ⟸   ENST00000639288
RefSeq Acc Id: ENSP00000465485   ⟸   ENST00000590785
RefSeq Acc Id: ENSP00000467675   ⟸   ENST00000460670
RefSeq Acc Id: ENSP00000410113   ⟸   ENST00000435416
RefSeq Acc Id: NP_001385420   ⟸   NM_001398491
- Peptide Label: isoform 1
- UniProtKB: Q96SR6 (UniProtKB/Swiss-Prot),   Q53ZY8 (UniProtKB/Swiss-Prot),   C9K0V5 (UniProtKB/Swiss-Prot),   A8MT55 (UniProtKB/Swiss-Prot),   A3KMP6 (UniProtKB/Swiss-Prot),   Q5JPJ2 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001385419   ⟸   NM_001398490
- Peptide Label: isoform 1
- UniProtKB: Q96SR6 (UniProtKB/Swiss-Prot),   Q53ZY8 (UniProtKB/Swiss-Prot),   C9K0V5 (UniProtKB/Swiss-Prot),   A8MT55 (UniProtKB/Swiss-Prot),   A3KMP6 (UniProtKB/Swiss-Prot),   Q5JPJ2 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001385421   ⟸   NM_001398492
- Peptide Label: isoform 2
Protein Domains
C2H2-type   KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96SR6-F1-model_v2 AlphaFold Q96SR6 1-550 view protein structure

Promoters
RGD ID:7239683
Promoter ID:EPDNEW_H25588
Type:initiation region
Name:ZNF382_3
Description:zinc finger protein 382
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H25587  EPDNEW_H25590  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,604,836 - 36,604,896EPDNEW
RGD ID:7239689
Promoter ID:EPDNEW_H25590
Type:initiation region
Name:ZNF382_1
Description:zinc finger protein 382
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H25588  EPDNEW_H25587  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,605,313 - 36,605,373EPDNEW
RGD ID:6796312
Promoter ID:HG_KWN:29741
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Jurkat,   K562,   Lymphoblastoid
Transcripts:NM_032825,   OTTHUMT00000340400,   OTTHUMT00000340401,   OTTHUMT00000340402,   UC010EFA.1,   UC010EFB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361941,787,776 - 41,788,402 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17409 AgrOrtholog
COSMIC ZNF382 COSMIC
Ensembl Genes ENSG00000161298 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000292928 ENTREZGENE
  ENST00000292928.7 UniProtKB/Swiss-Prot
  ENST00000423582.5 UniProtKB/TrEMBL
  ENST00000435416.1 UniProtKB/Swiss-Prot
  ENST00000439428 ENTREZGENE
  ENST00000439428.5 UniProtKB/Swiss-Prot
  ENST00000460670.5 UniProtKB/TrEMBL
  ENST00000590785.1 UniProtKB/TrEMBL
Gene3D-CATH 6.10.140.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000161298 GTEx
HGNC ID HGNC:17409 ENTREZGENE
Human Proteome Map ZNF382 Human Proteome Map
InterPro KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KRAB_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZNF781 UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:84911 UniProtKB/Swiss-Prot
NCBI Gene 84911 ENTREZGENE
OMIM 609516 OMIM
PANTHER C2H2-TYPE DOMAIN-CONTAINING PROTEIN UniProtKB/TrEMBL
  GH18834P-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR14947 UniProtKB/TrEMBL
  ZINC FINGER PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134869965 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
  ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF109640 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A3KMP6 ENTREZGENE
  A8MT55 ENTREZGENE
  C9JME7_HUMAN UniProtKB/TrEMBL
  C9K0V5 ENTREZGENE
  K7EK67_HUMAN UniProtKB/TrEMBL
  K7EQ52_HUMAN UniProtKB/TrEMBL
  L0R6T6_HUMAN UniProtKB/TrEMBL
  Q53ZY8 ENTREZGENE
  Q5JPJ2 ENTREZGENE
  Q96SR6 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A3KMP6 UniProtKB/Swiss-Prot
  A8MT55 UniProtKB/Swiss-Prot
  C9K0V5 UniProtKB/Swiss-Prot
  Q53ZY8 UniProtKB/Swiss-Prot
  Q5JPJ2 UniProtKB/Swiss-Prot