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References
Additional References at PubMed
Genomics
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Predicted Targets
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 TPMLow: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM
alimentary part of gastrointestinal system | circulatory system | exocrine system | hemolymphoid system | integumental system | musculoskeletal system | nervous system | reproductive system | respiratory system | sensory system | appendage | |
High | |||||||||||
Medium | |||||||||||
Low | 3 | 2 | 2 | 2 | 2 | 3 | 1 | 2 | |||
Below cutoff | 5 | 3 | 1 | 3 | 2 | 3 | 7 | 2 | 1 | 2 |
Sequence
Nucleotide Sequences
Reference Sequences
RefSeq Acc Id: | ENST00000385242 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | NR_030200 | ||||||||||||||||||||||||
RefSeq Status: | PROVISIONAL | ||||||||||||||||||||||||
Type: | NON-CODING | ||||||||||||||||||||||||
Position: |
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Sequence: |
Clinical Variants
Name | Type | Condition(s) | Position(s) | Clinical significance |
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 19q13.41-13.43(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 19q13.33-13.43(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 19q13.42(chr19:53692245-53808292)x3 | copy number gain | See cases [RCV000141357] | Chr19:53692245..53808292 [GRCh38] Chr19:54195499..54311546 [GRCh37] Chr19:58887311..59003358 [NCBI36] Chr19:19q13.42 |
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 |
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(chr19:49907832-58557889)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 19q13.42(chr19:53553042-53899466)x3 | copy number gain | See cases [RCV000052593] | Chr19:53553042..53899466 [GRCh38] Chr19:54056296..54402720 [GRCh37] Chr19:58748108..59094532 [NCBI36] Chr19:19q13.42 |
uncertain significance |
GRCh38/hg38 19q13.42(chr19:53601298-53773028)x3 | copy number gain | See cases [RCV000052594] | Chr19:53601298..53773028 [GRCh38] Chr19:54104552..54276282 [GRCh37] Chr19:58796364..58968094 [NCBI36] Chr19:19q13.42 |
uncertain significance |
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 |
NC_000019.9:g.54039784_54484439dup | duplication | Silver Russell Syndrome-related disorder [RCV000785667] | Chr19:53536530..53981185 [GRCh38] Chr19:54039784..54484439 [GRCh37] Chr19:19q13.42 |
uncertain significance |
Additional Information
External Database Links
Database | Acc Id | Source(s) |
COSMIC | MIR524 | COSMIC |
Ensembl Genes | ENSG00000283289 | Ensembl, ENTREZGENE |
Ensembl Transcript | ENST00000385242 | ENTREZGENE |
GTEx | ENSG00000283289 | GTEx |
HGNC ID | HGNC:32110 | ENTREZGENE |
Human Proteome Map | MIR524 | Human Proteome Map |
miRBase | MI0003160 | ENTREZGENE |
NCBI Gene | 574478 | ENTREZGENE |
PharmGKB | PA164722804 | PharmGKB |
RNAcentral | URS00003BD367 | RNACentral |
URS00003E236A | RNACentral | |
URS000063B6CA | RNACentral |