MIR192 (microRNA 192) - Rat Genome Database

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Gene: MIR192 (microRNA 192) Homo sapiens
Analyze
Symbol: MIR192
Name: microRNA 192
RGD ID: 1353067
HGNC Page HGNC:31562
Description: Enables mRNA 3'-UTR binding activity and mRNA base-pairing post-transcriptional repressor activity. Involved in miRNA-mediated gene silencing by mRNA destabilization; negative regulation of cell-matrix adhesion; and negative regulation of interleukin-21 production. Located in extracellular space. Biomarker of cholangiocarcinoma; malignant pleural mesothelioma; and opisthorchiasis.
Type: ncrna (Ensembl: miRNA)
RefSeq Status: PROVISIONAL
Previously known as: miR-192; MIRN192; miRNA192
RGD Orthologs
Mouse
Rat
Dog
Pig
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
GRCh381164,891,137 - 64,891,246 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1164,891,137 - 64,891,246 (-)Ensemblhg38GRCh38
GRCh371164,658,609 - 64,658,718 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361164,415,184 - 64,415,293 (-)NCBIBuild 36Build 36hg18NCBI36
Celera1161,984,676 - 61,984,785 (-)NCBICelera
Cytogenetic Map11q13.1NCBI
HuRef1160,985,641 - 60,985,750 (-)NCBIHuRef
CHM1_11164,542,391 - 64,542,500 (-)NCBICHM1_1
T2T-CHM13v2.01164,884,376 - 64,884,485 (-)NCBIT2T-CHM13v2.0
JBrowse:




Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Selection and Application of Tissue microRNAs for Nonendoscopic Diagnosis of Barrett's Esophagus. Li X, etal., Gastroenterology. 2018 Sep;155(3):771-783.e3. doi: 10.1053/j.gastro.2018.05.050. Epub 2018 Jun 12.
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. Urinary microRNA-192 and microRNA-21 as potential indicators for liver fluke-associated cholangiocarcinoma risk group. Silakit R, etal., Parasitol Int. 2017 Aug;66(4):479-485. doi: 10.1016/j.parint.2015.10.001. Epub 2015 Oct 9.
4. miR-193a-3p is a potential tumor suppressor in malignant pleural mesothelioma. Williams M, etal., Oncotarget. 2015 Sep 15;6(27):23480-95.
Additional References at PubMed
PMID:12554859   PMID:12554860   PMID:12624257   PMID:14573789   PMID:16381832   PMID:17604727   PMID:18766170   PMID:19074876   PMID:19088023   PMID:20056746   PMID:20647341   PMID:20889907  
PMID:21037258   PMID:21119604   PMID:21372198   PMID:21511813   PMID:21672525   PMID:21785383   PMID:22205577   PMID:22264233   PMID:22433310   PMID:23170939   PMID:23612862   PMID:23649428  
PMID:23715501   PMID:23737550   PMID:23737551   PMID:23743335   PMID:24012720   PMID:24213572   PMID:24223844   PMID:24508230   PMID:24623846   PMID:24791633   PMID:24854555   PMID:24981590  
PMID:25146671   PMID:25203061   PMID:25532038   PMID:25566965   PMID:25857602   PMID:26209011   PMID:26339371   PMID:26352740   PMID:26506238   PMID:26565986   PMID:26580097   PMID:26642352  
PMID:26646931   PMID:26684241   PMID:26710269   PMID:26743688   PMID:26747651   PMID:26881255   PMID:26942205   PMID:27079614   PMID:27153322   PMID:27216198   PMID:27279796   PMID:27304060  
PMID:27317768   PMID:27350618   PMID:27659777   PMID:27683056   PMID:28039611   PMID:28056546   PMID:28321538   PMID:28351309   PMID:28409330   PMID:28483554   PMID:28488550   PMID:28577875  
PMID:28798470   PMID:28884252   PMID:28945992   PMID:29034845   PMID:29239144   PMID:29471417   PMID:29490514   PMID:29529220   PMID:29536411   PMID:29571988   PMID:29578116   PMID:29689705  
PMID:29845236   PMID:30006518   PMID:30024615   PMID:30059664   PMID:30142428   PMID:30250222   PMID:30332302   PMID:30366671   PMID:30530815   PMID:30544100   PMID:30595117   PMID:30628692  
PMID:30844143   PMID:31020657   PMID:31229581   PMID:31450012   PMID:31485620   PMID:31561425   PMID:31629394   PMID:31775784   PMID:31873114   PMID:31918268   PMID:32013999   PMID:32076107  
PMID:32091625   PMID:32102564   PMID:32106776   PMID:32210284   PMID:32307002   PMID:32406504   PMID:32965165   PMID:33024199   PMID:33097010   PMID:33256802   PMID:33325098   PMID:33499877  
PMID:33614788   PMID:33639203   PMID:33735626   PMID:33986456   PMID:34042256   PMID:34085163   PMID:34104082   PMID:34256371   PMID:34296287   PMID:34296808   PMID:34357569   PMID:34486645  
PMID:34715618   PMID:34716242   PMID:34717195   PMID:34906278   PMID:35000146   PMID:35109781   PMID:35893704   PMID:35976169   PMID:35992154   PMID:36254230   PMID:36803590   PMID:36861382  
PMID:37396169   PMID:37585722   PMID:37903058   PMID:38044851   PMID:38254634   PMID:38486141   PMID:38717494  


Genomics

Comparative Map Data
MIR192
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381164,891,137 - 64,891,246 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1164,891,137 - 64,891,246 (-)Ensemblhg38GRCh38
GRCh371164,658,609 - 64,658,718 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361164,415,184 - 64,415,293 (-)NCBIBuild 36Build 36hg18NCBI36
Celera1161,984,676 - 61,984,785 (-)NCBICelera
Cytogenetic Map11q13.1NCBI
HuRef1160,985,641 - 60,985,750 (-)NCBIHuRef
CHM1_11164,542,391 - 64,542,500 (-)NCBICHM1_1
T2T-CHM13v2.01164,884,376 - 64,884,485 (-)NCBIT2T-CHM13v2.0
Mir192
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39196,314,874 - 6,314,962 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl196,314,874 - 6,314,962 (+)EnsemblGRCm39 EnsemblGRCm39
GRCm38196,264,844 - 6,264,932 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl196,264,844 - 6,264,932 (+)Ensemblmm10GRCm38
MGSCv37196,264,844 - 6,264,932 (+)NCBIMGSCv37MGSCv37mm9NCBIm37
Celera196,137,173 - 6,137,261 (+)NCBICelera
Cytogenetic Map19ANCBI
cM Map194.39NCBI
Mir192
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81212,994,209 - 212,994,318 (+)NCBIGRCr8GRCr8GRCr8
GRCr8 Ensembl1212,994,209 - 212,994,318 (+)EnsemblGRCr8
mRatBN7.21203,564,946 - 203,565,055 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1203,564,946 - 203,565,055 (+)EnsemblmRatBN7.2
UTH_Rnor_SHR_Utx1211,913,950 - 211,914,059 (+)NCBIUTH_Rnor_SHR_UtxUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01219,010,277 - 219,010,386 (+)NCBIUTH_Rnor_SHRSP_BbbUtx_1.0UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01211,701,334 - 211,701,443 (+)NCBIUTH_Rnor_WKY_Bbb_1.0UTH_Rnor_WKY_Bbb_1.0
Rnor_6.01221,634,971 - 221,635,080 (+)NCBIRnor_6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1221,634,971 - 221,635,080 (+)Ensemblrn6Rnor6.0
Rnor_5.01228,620,072 - 228,620,181 (+)NCBIRnor_5.0Rnor_5.0rn5
Celera1201,098,481 - 201,098,590 (+)NCBICelera
Cytogenetic Map1q43NCBI
MIR192
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11852,281,129 - 52,281,193 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1852,281,129 - 52,281,193 (+)EnsemblcanFam3CanFam3.1
Dog10K_Boxer_Tasha1850,888,461 - 50,888,525 (+)NCBIDog10K_Boxer_TashaDog10K_Boxer_Tasha
ROS_Cfam_1.01853,322,283 - 53,322,347 (+)NCBIROS_Cfam_1.0ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1853,322,283 - 53,322,347 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11852,417,276 - 52,417,340 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01852,002,572 - 52,002,636 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01852,786,986 - 52,787,050 (+)NCBIUU_Cfam_GSD_1.0UU_Cfam_GSD_1.0
MIR192
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl27,285,667 - 7,285,746 (+)EnsemblsusScr11Sscrofa11.1
Sscrofa11.127,285,667 - 7,285,746 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.226,416,980 - 6,417,059 (+)NCBISscrofa10.2Sscrofa10.2susScr3


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh37/hg19 11q13.1(chr11:64485197-64691737)x3 copy number gain See cases [RCV000203413] Chr11:64485197..64691737 [GRCh37]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11q13.1-13.2(chr11:64501919-67129258)x3 copy number gain See cases [RCV000511632] Chr11:64501919..67129258 [GRCh37]
Chr11:11q13.1-13.2		 likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
dup(11)(q13.1q13.1) duplication Ependymoma [RCV000785872] Chr11:63533279..65429676 [GRCh37]
Chr11:11q13.1		 likely pathogenic
GRCh37/hg19 11q13.1(chr11:64396501-64883447)x3 copy number gain not provided [RCV000848683] Chr11:64396501..64883447 [GRCh37]
Chr11:11q13.1		 uncertain significance
NC_000011.9:g.(?_59596957)_(68707199_?)dup duplication Familial temporal lobe epilepsy 8 [RCV001372442] Chr11:59596957..68707199 [GRCh37]
Chr11:11q12.1-13.3		 uncertain significance
NC_000011.9:g.(?_64522783)_(66283694_?)del deletion Bardet-Biedl syndrome [RCV002014493]|Glycogen storage disease, type V [RCV002004587] Chr11:64522783..66283694 [GRCh37]
Chr11:11q13.1-13.2		 pathogenic
NC_000011.9:g.(?_58916346)_(64972349_?)dup duplication Leukocyte adhesion deficiency 3 [RCV003113394]|not provided [RCV003113393] Chr11:58916346..64972349 [GRCh37]
Chr11:11q12.1-13.1		 uncertain significance|no classifications from unflagged records
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3 copy number gain not provided [RCV003484842] Chr11:59923608..76272324 [GRCh37]
Chr11:11q12.2-13.5		 pathogenic
GRCh37/hg19 11q13.1(chr11:64557855-64741375)x3 copy number gain not provided [RCV003484843] Chr11:64557855..64741375 [GRCh37]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11q13.1(chr11:64573225-65193732)x3 copy number gain not provided [RCV003484844] Chr11:64573225..65193732 [GRCh37]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3 copy number gain not specified [RCV003986944] Chr11:56895955..69295402 [GRCh37]
Chr11:11q12.1-13.3		 likely pathogenic
miRNA Target Status (No longer updated)

Confirmed Targets
Gene TargetMature miRNAMethod NameResult TypeData TypeSupport TypePMID
ERCC4hsa-miR-192-5pMirtarbaseexternal_infoMicroarrayFunctional MTI (Weak)19074876
RB1hsa-miR-192-5pMirtarbaseexternal_infoImmunoblot//Luciferase reporter assay//qRT-PCR//WeFunctional MTI21511813
ACVR2Bhsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assay//Western blotFunctional MTI22431721
CLIC1hsa-miR-192-5pMirtarbaseexternal_infoMicroarrayFunctional MTI (Weak)16822819
BCL2hsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assay//qRT-PCR//Reporter assayFunctional MTI19074876
CDC7hsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assay//qRT-PCR//Western blot//Functional MTI19074876
HOXA10hsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assay//qRT-PCRFunctional MTI19074876
PIM1hsa-miR-192-5pMirtarbaseexternal_infoSequencingFunctional MTI (Weak)20371350
RACGAP1hsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assay//qRT-PCR//Microarray//ReFunctional MTI19074876
CDKN1Bhsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assayNon-Functional MTI17627278
WNK1hsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assay//Northern blot//qRT-PCR/Functional MTI20813867
ATP1B1hsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI23221637
BRWD1hsa-miR-192-5pMirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248
PLCE1hsa-miR-192-5pTarbaseexternal_infoMicroarrayPOSITIVE
CUL5hsa-miR-192-5pTarbaseexternal_infoReporter GenePOSITIVE
CUL5hsa-miR-192-5pTarbaseexternal_infoWesternblitPOSITIVE
PIGMhsa-miR-192-5pTarbaseexternal_infoSequencingPOSITIVE
DHFRhsa-miR-192-5pMirecordsexternal_info{unchanged}NA19088023
RB1hsa-miR-192-5pMirecordsexternal_info{changed}NA21511813
ACVR2Bhsa-miR-192-5pOncomiRDBexternal_infoNANA22431721
ERCC3hsa-miR-192-5pOncomiRDBexternal_infoNANA21672525
RB1hsa-miR-192-5pOncomiRDBexternal_infoNANA21511813
ALCAMhsa-miR-192-5pOncomiRDBexternal_infoNANA21119604
MDM2hsa-miR-192-5pOncomiRDBexternal_infoNANA20951946
DHFRhsa-miR-192-5pOncomiRDBexternal_infoNANA19088023
ZEB1hsa-miR-192-5pOncomiRDBexternal_infoNANA18805502
ERCC4hsa-miR-192-5pMirtarbaseexternal_infoLuciferase reporter assay//qRT-PCR//Western blotFunctional MTI21672525

Predicted Targets
Summary Value
Count of predictions:13928
Count of gene targets:6381
Count of transcripts:11434
Interacting mature miRNAs:hsa-miR-192-3p, hsa-miR-192-5p
Prediction methods:Microtar, Miranda, Pita, Rnahybrid, Targetscan
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1357380BW64_HBody weight QTL 64 (human)2.2Body weightpercent fat after exercise training116097893786978937Human

Markers in Region
ECD00132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,658,555 - 64,659,487UniSTSGRCh37
Build 361164,415,131 - 64,416,063RGDNCBI36
Celera1161,984,622 - 61,985,554RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,985,587 - 60,986,519UniSTS
ECD23426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,659,792 - 64,659,981UniSTSGRCh37
Build 361164,416,368 - 64,416,557RGDNCBI36
Celera1161,985,859 - 61,986,048RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,986,824 - 60,987,013UniSTS
REN56877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,658,151 - 64,658,399UniSTSGRCh37
Build 361164,414,727 - 64,414,975RGDNCBI36
Celera1161,984,218 - 61,984,466RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,985,183 - 60,985,431UniSTS
REN56878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,658,396 - 64,658,645UniSTSGRCh37
Build 361164,414,972 - 64,415,221RGDNCBI36
Celera1161,984,463 - 61,984,712RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,985,428 - 60,985,677UniSTS
REN56879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,658,622 - 64,658,860UniSTSGRCh37
Build 361164,415,198 - 64,415,436RGDNCBI36
Celera1161,984,689 - 61,984,927RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,985,654 - 60,985,892UniSTS
REN56880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,658,807 - 64,659,042UniSTSGRCh37
Build 361164,415,383 - 64,415,618RGDNCBI36
Celera1161,984,874 - 61,985,109RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,985,839 - 60,986,074UniSTS
REN56881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,659,019 - 64,659,268UniSTSGRCh37
Build 361164,415,595 - 64,415,844RGDNCBI36
Celera1161,985,086 - 61,985,335RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,986,051 - 60,986,300UniSTS
REN56882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,659,247 - 64,659,507UniSTSGRCh37
Build 361164,415,823 - 64,416,083RGDNCBI36
Celera1161,985,314 - 61,985,574RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,986,279 - 60,986,539UniSTS
REN56883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,659,484 - 64,659,735UniSTSGRCh37
Build 361164,416,060 - 64,416,311RGDNCBI36
Celera1161,985,551 - 61,985,802RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,986,516 - 60,986,767UniSTS
REN56884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,659,743 - 64,659,968UniSTSGRCh37
Build 361164,416,319 - 64,416,544RGDNCBI36
Celera1161,985,810 - 61,986,035RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,986,775 - 60,987,000UniSTS
REN56885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,659,943 - 64,660,204UniSTSGRCh37
Build 361164,416,519 - 64,416,780RGDNCBI36
Celera1161,986,010 - 61,986,271RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,986,975 - 60,987,236UniSTS
REN56886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,660,197 - 64,660,446UniSTSGRCh37
Build 361164,416,773 - 64,417,022RGDNCBI36
Celera1161,986,264 - 61,986,513RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,987,229 - 60,987,478UniSTS
REN56887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,660,301 - 64,660,551UniSTSGRCh37
Build 361164,416,877 - 64,417,127RGDNCBI36
Celera1161,986,368 - 61,986,618RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,987,333 - 60,987,583UniSTS


Expression

RNA-SEQ Expression


Sequence


Ensembl Acc Id: ENST00000384915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1164,891,137 - 64,891,246 (-)Ensembl
RefSeq Acc Id: NR_029578
RefSeq Status: PROVISIONAL
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381164,891,137 - 64,891,246 (-)NCBI
GRCh371164,658,609 - 64,658,718 (-)RGD
Celera1161,984,676 - 61,984,785 (-)RGD
HuRef1160,985,641 - 60,985,750 (-)ENTREZGENE
CHM1_11164,542,391 - 64,542,500 (-)NCBI
T2T-CHM13v2.01164,884,376 - 64,884,485 (-)NCBI
Sequence:

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:31562 AgrOrtholog
COSMIC MIR192 COSMIC
Ensembl Genes ENSG00000283926 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000384915 ENTREZGENE
GTEx ENSG00000283926 GTEx
HGNC ID HGNC:31562 ENTREZGENE
Human Proteome Map MIR192 Human Proteome Map
miRBase MI0000234 ENTREZGENE
NCBI Gene 406967 ENTREZGENE
OMIM 610939 OMIM
PharmGKB PA164722550 PharmGKB
RNAcentral URS00000B59A2 RNACentral
  URS0000155642 RNACentral
  URS00006ECF62 RNACentral