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References
References - curated
Additional References at PubMed
Genomics
miRNA Target Status
Predicted Targets
Summary Value | Count of predictions: | 72705 | Count of gene targets: | 20165 | Count of transcripts: | 50556 | Interacting mature miRNAs: | hsa-miR-4700-3p, hsa-miR-4700-5p | 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. |
Expression
Sequence
Nucleotide Sequences
Reference Sequences
RefSeq Acc Id: | ENST00000578311 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | NR_039849 | ||||||||||||||||||||
RefSeq Status: | PROVISIONAL | ||||||||||||||||||||
Type: | NON-CODING | ||||||||||||||||||||
Position: |
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Sequence: |
Clinical Variants
Name | Type | Condition(s) | Position(s) | Clinical significance |
NM_001080533.2(UNC119B):c.664C>T (p.Pro222Ser) | single nucleotide variant | Malignant melanoma [RCV000069853] | Chr12:120719940 [GRCh38] Chr12:121157743 [GRCh37] Chr12:119642126 [NCBI36] Chr12:12q24.31 |
not provided |
GRCh38/hg38 12q24.31-24.33(chr12:120697672-133202490)x3 | copy number gain | See cases [RCV000137651] | Chr12:120697672..133202490 [GRCh38] Chr12:121135475..133779076 [GRCh37] Chr12:119619858..132289149 [NCBI36] Chr12:12q24.31-24.33 |
pathogenic |
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 | copy number gain | See cases [RCV000139555] | Chr12:121271..133196807 [GRCh38] Chr12:282465..133773393 [GRCh37] Chr12:100698..132283466 [NCBI36] Chr12:12p13.33-q24.33 |
pathogenic |
GRCh38/hg38 12q24.31-24.32(chr12:120718786-127500215)x1 | copy number loss | See cases [RCV000142454] | Chr12:120718786..127500215 [GRCh38] Chr12:121156589..127984760 [GRCh37] Chr12:119640972..126550713 [NCBI36] Chr12:12q24.31-24.32 |
pathogenic |
GRCh38/hg38 12q24.21-24.33(chr12:114268403-133201316)x3 | copy number gain | See cases [RCV000143656] | Chr12:114268403..133201316 [GRCh38] Chr12:114706208..133777902 [GRCh37] Chr12:113190591..132287975 [NCBI36] Chr12:12q24.21-24.33 |
pathogenic |
GRCh38/hg38 12q24.31(chr12:120504068-122459718)x1 | copy number loss | See cases [RCV000051342] | Chr12:120504068..122459718 [GRCh38] Chr12:120941871..122944265 [GRCh37] Chr12:119426254..121510218 [NCBI36] Chr12:12q24.31 |
pathogenic |
GRCh38/hg38 12q24.23-24.33(chr12:118165459-133182322)x3 | copy number gain | See cases [RCV000050866] | Chr12:118165459..133182322 [GRCh38] Chr12:118603264..133758908 [GRCh37] Chr12:117087647..132268981 [NCBI36] Chr12:12q24.23-24.33 |
pathogenic |
GRCh38/hg38 12q24.23-24.31(chr12:119286893-122638552)x3 | copy number gain | See cases [RCV000051981] | Chr12:119286893..122638552 [GRCh38] Chr12:119724698..123123099 [GRCh37] Chr12:118209081..121689052 [NCBI36] Chr12:12q24.23-24.31 |
uncertain significance |
GRCh38/hg38 12q24.21-24.33(chr12:115131583-133166920)x3 | copy number gain | See cases [RCV000053689] | Chr12:115131583..133166920 [GRCh38] Chr12:115569388..133743506 [GRCh37] Chr12:114053771..132253579 [NCBI36] Chr12:12q24.21-24.33 |
pathogenic |
GRCh38/hg38 12q24.23-24.33(chr12:119417382-133191400)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053691]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053691]|See cases [RCV000053691] | Chr12:119417382..133191400 [GRCh38] Chr12:119855187..133767986 [GRCh37] Chr12:118339570..132278059 [NCBI36] Chr12:12q24.23-24.33 |
pathogenic |
Additional Information
External Database Links
Database | Acc Id | Source(s) |
COSMIC | MIR4700 | COSMIC |
Ensembl Genes | ENSG00000284143 | Ensembl, ENTREZGENE |
Ensembl Transcript | ENST00000578311 | ENTREZGENE |
GTEx | ENSG00000284143 | GTEx |
HGNC ID | HGNC:41806 | ENTREZGENE |
Human Proteome Map | MIR4700 | Human Proteome Map |
miRBase | MI0017333 | ENTREZGENE |
NCBI Gene | 100616329 | ENTREZGENE |
RNAcentral | URS0000334286 | RNACentral |
URS00003840E5 | RNACentral | |
URS000075B578 | RNACentral |