MIR1322 (microRNA 1322) - Rat Genome Database
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Gene: MIR1322 (microRNA 1322) Homo sapiens
Analyze
Symbol: MIR1322
Name: microRNA 1322
RGD ID: 2312958
HGNC Page HGNC
Description: microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]
Type: ncrna
RefSeq Status: PROVISIONAL
Also known as: hsa-mir-1322; MIRN1322
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl810,825,373 - 10,825,443 (-)EnsemblGRCh38hg38GRCh38
GRCh38810,825,373 - 10,825,443 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37810,682,883 - 10,682,953 (-)NCBIGRCh37GRCh37hg19GRCh37
Celera89,810,916 - 9,810,986 (-)NCBI
Cytogenetic Map8p23.1NCBI
HuRef89,613,090 - 9,613,160 (-)NCBIHuRef
CHM1_1810,748,100 - 10,748,170 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
References
Additional References at PubMed
PMID:16381832   PMID:18230126   PMID:20686565   PMID:22315007   PMID:24097068   PMID:26114118   PMID:30079502  


Genomics

miRNA Target Status

Confirmed Targets
Gene TargetMature miRNAMethod NameResult TypeData TypeSupport TypePMID
SPINK7hsa-miR-1322OncomiRDBexternal_infoNANA22315007

Predicted Targets
Summary Value
Count of predictions:7956
Count of gene targets:4086
Count of transcripts:6990
Interacting mature miRNAs:hsa-miR-1322
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.


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 hemolymphoid system integumental system musculoskeletal system nervous system adipose tissue appendage
High
Medium 2
Low 1 30 2
Below cutoff 1 1 2 1 1 1 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000638013
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl810,825,373 - 10,825,443 (-)Ensembl
RefSeq Acc Id: NR_031711
RefSeq Status: PROVISIONAL
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38810,825,373 - 10,825,443 (-)NCBI
GRCh37810,682,883 - 10,682,953 (-)RGD
Celera89,810,916 - 9,810,986 (-)RGD
HuRef89,613,090 - 9,613,160 (-)ENTREZGENE
CHM1_1810,748,100 - 10,748,170 (-)NCBI
Sequence:

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8p23.1(chr8:8222339-12182465)x1 copy number loss See cases [RCV000053169] Chr8:8222339..12182465 [GRCh38]
Chr8:8079861..12039974 [GRCh37]
Chr8:8117271..12077383 [NCBI36]
Chr8:8p23.1
pathogenic|likely pathogenic|conflicting data from submitters
GRCh38/hg38 8p23.1(chr8:8273108-11948451)x3 copy number gain See cases [RCV000053484] Chr8:8273108..11948451 [GRCh38]
Chr8:8130630..11805960 [GRCh37]
Chr8:8168040..11843369 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:7834379-12182465)x3 copy number gain See cases [RCV000134177] Chr8:7834379..12182465 [GRCh38]
Chr8:7691901..12039974 [GRCh37]
Chr8:7729311..12077383 [NCBI36]
Chr8:8p23.1
pathogenic|likely pathogenic
GRCh38/hg38 8p23.1(chr8:8545843-11814470)x1 copy number loss See cases [RCV000134092] Chr8:8545843..11814470 [GRCh38]
Chr8:8403353..11671979 [GRCh37]
Chr8:8440763..11709388 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:8273108-12546553)x3 copy number gain See cases [RCV000134923] Chr8:8273108..12546553 [GRCh38]
Chr8:8130630..12404062 [GRCh37]
Chr8:8168040..12448433 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:8273108-11948451)x1 copy number loss See cases [RCV000135749] Chr8:8273108..11948451 [GRCh38]
Chr8:8130630..11805960 [GRCh37]
Chr8:8168040..11843369 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:8273108-12383643)x1 copy number loss See cases [RCV000135775] Chr8:8273108..12383643 [GRCh38]
Chr8:8130630..12241152 [GRCh37]
Chr8:8168040..12285523 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:241530-10867132)x1 copy number loss See cases [RCV000135534] Chr8:241530..10867132 [GRCh38]
Chr8:191530..10724642 [GRCh37]
Chr8:181530..10762052 [NCBI36]
Chr8:8p23.3-23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:7311968-12546553)x3 copy number gain See cases [RCV000136522] Chr8:7311968..12546553 [GRCh38]
Chr8:7169490..12404062 [GRCh37]
Chr8:7156900..12448433 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:7311968-12546553)x1 copy number loss See cases [RCV000136523] Chr8:7311968..12546553 [GRCh38]
Chr8:7169490..12404062 [GRCh37]
Chr8:7156900..12448433 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.3-21.3(chr8:241530-23198398)x3 copy number gain See cases [RCV000135967] Chr8:241530..23198398 [GRCh38]
Chr8:191530..23055911 [GRCh37]
Chr8:181530..23111856 [NCBI36]
Chr8:8p23.3-21.3
pathogenic
GRCh38/hg38 8p23.3-21.2(chr8:241605-24656971)x3 copy number gain See cases [RCV000136026] Chr8:241605..24656971 [GRCh38]
Chr8:191605..24514484 [GRCh37]
Chr8:181605..24570374 [NCBI36]
Chr8:8p23.3-21.2
pathogenic
GRCh38/hg38 8p23.1(chr8:8253505-12610034)x1 copy number loss See cases [RCV000137505] Chr8:8253505..12610034 [GRCh38]
Chr8:8111027..12467543 [GRCh37]
Chr8:8148437..12511914 [NCBI36]
Chr8:8p23.1
pathogenic|likely benign
GRCh38/hg38 8p23.3-23.1(chr8:226452-12712987)x3 copy number gain See cases [RCV000137984] Chr8:226452..12712987 [GRCh38]
Chr8:176452..12570496 [GRCh37]
Chr8:166452..12614867 [NCBI36]
Chr8:8p23.3-23.1
pathogenic
GRCh38/hg38 8p23.3-11.23(chr8:226452-38021728)x3 copy number gain See cases [RCV000137807] Chr8:226452..38021728 [GRCh38]
Chr8:176452..37879246 [GRCh37]
Chr8:166452..37998403 [NCBI36]
Chr8:8p23.3-11.23
pathogenic|likely pathogenic
GRCh38/hg38 8p23.1(chr8:8222339-12050329)x3 copy number gain See cases [RCV000137864] Chr8:8222339..12050329 [GRCh38]
Chr8:8079861..11907838 [GRCh37]
Chr8:8117271..11945247 [NCBI36]
Chr8:8p23.1
likely pathogenic
GRCh38/hg38 8p23.3-12(chr8:241605-31091074)x3 copy number gain See cases [RCV000138831] Chr8:241605..31091074 [GRCh38]
Chr8:191605..30948590 [GRCh37]
Chr8:181605..31068132 [NCBI36]
Chr8:8p23.3-12
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.1(chr8:7103661-12299882)x3 copy number gain See cases [RCV000138529] Chr8:7103661..12299882 [GRCh38]
Chr8:6961183..12157391 [GRCh37]
Chr8:6948593..12201760 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:8253505-12003060)x1 copy number loss See cases [RCV000138559] Chr8:8253505..12003060 [GRCh38]
Chr8:8111027..11860569 [GRCh37]
Chr8:8148437..11897978 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.2-23.1(chr8:3934205-11526939)x1 copy number loss See cases [RCV000138943] Chr8:3934205..11526939 [GRCh38]
Chr8:3791727..11384448 [GRCh37]
Chr8:3779135..11421857 [NCBI36]
Chr8:8p23.2-23.1
pathogenic
GRCh38/hg38 8p23.1-11.22(chr8:7141697-38695546)x3 copy number gain See cases [RCV000139891] Chr8:7141697..38695546 [GRCh38]
Chr8:6999219..38553064 [GRCh37]
Chr8:6986629..38672221 [NCBI36]
Chr8:8p23.1-11.22
pathogenic
GRCh38/hg38 8p23.1(chr8:10379998-10970694)x3 copy number gain See cases [RCV000139604] Chr8:10379998..10970694 [GRCh38]
Chr8:10237508..10828204 [GRCh37]
Chr8:10274918..10865614 [NCBI36]
Chr8:8p23.1
uncertain significance
GRCh38/hg38 8p23.3-12(chr8:226452-34491890)x3 copy number gain See cases [RCV000141410] Chr8:226452..34491890 [GRCh38]
Chr8:176452..34349408 [GRCh37]
Chr8:166452..34468950 [NCBI36]
Chr8:8p23.3-12
pathogenic
GRCh38/hg38 8p23.3-22(chr8:226452-16280146)x3 copy number gain See cases [RCV000141418] Chr8:226452..16280146 [GRCh38]
Chr8:176452..16137655 [GRCh37]
Chr8:166452..16182026 [NCBI36]
Chr8:8p23.3-22
pathogenic
GRCh38/hg38 8p23.1(chr8:8253505-11422633)x1 copy number loss See cases [RCV000141377] Chr8:8253505..11422633 [GRCh38]
Chr8:8111027..11280142 [GRCh37]
Chr8:8148437..11317552 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:10510192-12003060)x3 copy number gain See cases [RCV000140847] Chr8:10510192..12003060 [GRCh38]
Chr8:10367702..11860569 [GRCh37]
Chr8:10405112..11897978 [NCBI36]
Chr8:8p23.1
uncertain significance
GRCh38/hg38 8p23.1(chr8:8222339-11984333)x1 copy number loss See cases [RCV000140886] Chr8:8222339..11984333 [GRCh38]
Chr8:8079861..11841842 [GRCh37]
Chr8:8117271..11879251 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:8235647-12037723)x1 copy number loss See cases [RCV000141976] Chr8:8235647..12037723 [GRCh38]
Chr8:8093169..11895232 [GRCh37]
Chr8:8130579..11932641 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.1(chr8:8764178-11063564)x3 copy number gain See cases [RCV000141557] Chr8:8764178..11063564 [GRCh38]
Chr8:8621688..10921074 [GRCh37]
Chr8:8659098..10958484 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:9456230-11013618)x1 copy number loss See cases [RCV000141459] Chr8:9456230..11013618 [GRCh38]
Chr8:9313740..10871128 [GRCh37]
Chr8:9351150..10908538 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.1(chr8:8273108-12610034)x1 copy number loss See cases [RCV000142710] Chr8:8273108..12610034 [GRCh38]
Chr8:8130630..12467543 [GRCh37]
Chr8:8168040..12511914 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:8235647-12077956)x1 copy number loss See cases [RCV000143356] Chr8:8235647..12077956 [GRCh38]
Chr8:8093169..11935465 [GRCh37]
Chr8:8130579..11972874 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:8235544-12088347)x3 copy number gain See cases [RCV000143280] Chr8:8235544..12088347 [GRCh38]
Chr8:8093066..11945856 [GRCh37]
Chr8:8130476..11983265 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:226452-12698554)x3 copy number gain See cases [RCV000143248] Chr8:226452..12698554 [GRCh38]
Chr8:176452..12556063 [GRCh37]
Chr8:166452..12600434 [NCBI36]
Chr8:8p23.3-23.1
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.1(chr8:8222339-12182465)x1 copy number loss See cases [RCV000148286] Chr8:8222339..12182465 [GRCh38]
Chr8:8079861..12039974 [GRCh37]
Chr8:8117271..12077383 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.2-21.1(chr8:2475295-27504279)x1 copy number loss See cases [RCV000148252] Chr8:2475295..27504279 [GRCh38]
Chr8:2292235..27361796 [GRCh37]
Chr8:2121457..27417713 [NCBI36]
Chr8:8p23.2-21.1
pathogenic
GRCh38/hg38 8p23.1(chr8:7411297-12182465)x3 copy number gain See cases [RCV000051192] Chr8:7411297..12182465 [GRCh38]
Chr8:7268819..12039974 [GRCh37]
Chr8:7256229..12077383 [NCBI36]
Chr8:8p23.1
pathogenic|uncertain significance
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.1(chr8:8222339-12383643)x1 copy number loss See cases [RCV000050658] Chr8:8222339..12383643 [GRCh38]
Chr8:8079861..12241152 [GRCh37]
Chr8:8117271..12285523 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.3-21.1(chr8:2475295-27504279)x1 copy number loss See cases [RCV000050297] Chr8:2475295..27504279 [GRCh38]
Chr8:2292235..27361796 [GRCh37]
Chr8:2121457..27417713 [NCBI36]
Chr8:8p23.3-21.1
pathogenic
GRCh38/hg38 8p23.1(chr8:9970431-11984392)x3 copy number gain See cases [RCV000052154] Chr8:9970431..11984392 [GRCh38]
Chr8:9827941..11841901 [GRCh37]
Chr8:9865351..11879310 [NCBI36]
Chr8:8p23.1
pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:10056979-11573632)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052155]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052155]|See cases [RCV000052155] Chr8:10056979..11573632 [GRCh38]
Chr8:9914489..11431141 [GRCh37]
Chr8:9951899..11468550 [NCBI36]
Chr8:8p23.1
uncertain significance
GRCh38/hg38 8p23.1(chr8:10094463-11518412)x3 copy number gain See cases [RCV000052156] Chr8:10094463..11518412 [GRCh38]
Chr8:9951973..11375921 [GRCh37]
Chr8:9989383..11413330 [NCBI36]
Chr8:8p23.1
uncertain significance
GRCh38/hg38 8p23.1(chr8:8222139-12383784)x3 copy number gain See cases [RCV000053482] Chr8:8222139..12383784 [GRCh38]
Chr8:8079661..12241293 [GRCh37]
Chr8:8117071..12285664 [NCBI36]
Chr8:8p23.1
pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:8272908-12182621)x3 copy number gain See cases [RCV000053483] Chr8:8272908..12182621 [GRCh38]
Chr8:8130430..12040130 [GRCh37]
Chr8:8167840..12077539 [NCBI36]
Chr8:8p23.1
pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:8336212-11984392)x3 copy number gain See cases [RCV000053485] Chr8:8336212..11984392 [GRCh38]
Chr8:8193728..11841901 [GRCh37]
Chr8:8231138..11879310 [NCBI36]
Chr8:8p23.1
pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:8336212-11984392)x1 copy number loss See cases [RCV000053486] Chr8:8336212..11984392 [GRCh38]
Chr8:8193728..11841901 [GRCh37]
Chr8:8231138..11879310 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:8336212-12021806)x3 copy number gain See cases [RCV000053489] Chr8:8336212..12021806 [GRCh38]
Chr8:8193728..11879315 [GRCh37]
Chr8:8231138..11916724 [NCBI36]
Chr8:8p23.1
pathogenic|uncertain significance
GRCh38/hg38 8p23.3-12(chr8:96310-30614703)x3 copy number gain See cases [RCV000053599] Chr8:96310..30614703 [GRCh38]
Chr8:46310..30472220 [GRCh37]
Chr8:36310..30591762 [NCBI36]
Chr8:8p23.3-12
pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:96310-12021806)x3 copy number gain See cases [RCV000053600] Chr8:96310..12021806 [GRCh38]
Chr8:46310..11879315 [GRCh37]
Chr8:36310..11916724 [NCBI36]
Chr8:8p23.3-23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:7195664-12383643)x1 copy number loss See cases [RCV000053154] Chr8:7195664..12383643 [GRCh38]
Chr8:7053186..12241152 [GRCh37]
Chr8:7040596..12285523 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-22(chr8:241530-17678697)x3 copy number gain See cases [RCV000053603] Chr8:241530..17678697 [GRCh38]
Chr8:191530..17536206 [GRCh37]
Chr8:181530..17580486 [NCBI36]
Chr8:8p23.3-22
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.1(chr8:7234837-12514815)x1 copy number loss See cases [RCV000053165] Chr8:7234837..12514815 [GRCh38]
Chr8:7092359..12372324 [GRCh37]
Chr8:7079769..12416695 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:7411097-12610175)x1 copy number loss See cases [RCV000053166] Chr8:7411097..12610175 [GRCh38]
Chr8:7268619..12467684 [GRCh37]
Chr8:7256029..12512055 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:7411297-11961807)x1 copy number loss See cases [RCV000053167] Chr8:7411297..11961807 [GRCh38]
Chr8:7268819..11819316 [GRCh37]
Chr8:7256229..11856725 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:7411297-12546553)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053168]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053168]|See cases [RCV000053168] Chr8:7411297..12546553 [GRCh38]
Chr8:7268819..12404062 [GRCh37]
Chr8:7256229..12448433 [NCBI36]
Chr8:8p23.1
pathogenic
GRCh38/hg38 8p23.1(chr8:9924272-11573632)x1 copy number loss See cases [RCV000054226] Chr8:9924272..11573632 [GRCh38]
Chr8:9781782..11431141 [GRCh37]
Chr8:9819192..11468550 [NCBI36]
Chr8:8p23.1
pathogenic

Additional Information

Database Acc Id Source(s)
COSMIC MIR1322 COSMIC
Ensembl Genes ENSG00000283210 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000638013 ENTREZGENE
GTEx ENSG00000283210 GTEx
HGNC ID HGNC:35374 ENTREZGENE
Human Proteome Map MIR1322 Human Proteome Map
miRBase MI0006653 ENTREZGENE
NCBI Gene 100302166 ENTREZGENE
PharmGKB PA164722474 PharmGKB
RNAcentral URS000075B7CC RNACentral
  URS000075DEC8 RNACentral