LINC01725 (long intergenic non-protein coding RNA 1725) - Rat Genome Database

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Gene: LINC01725 (long intergenic non-protein coding RNA 1725) Homo sapiens
Analyze
Symbol: LINC01725
Name: long intergenic non-protein coding RNA 1725
RGD ID: 11563594
Description:
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38183,801,516 - 83,860,546 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl183,575,776 - 83,861,053 (-)EnsemblGRCh38hg38GRCh38
GRCh37184,267,199 - 84,326,229 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map1p31.1NCBI
HuRef182,384,301 - 82,443,167 (-)NCBIHuRef
CHM1_1184,381,857 - 84,440,965 (-)NCBICHM1_1
T2T-CHM13v2.0183,641,830 - 83,700,893 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


References
Additional References at PubMed
PMID:14702039  


Genomics

Variants

.
Variants in LINC01725
1 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p31.1-21.1(chr1:83457325-104273917)x3 copy number gain See cases [RCV000135654] Chr1:83457325..104273917 [GRCh38]
Chr1:83923008..104816539 [GRCh37]
Chr1:83695596..104618062 [NCBI36]
Chr1:1p31.1-21.1
pathogenic
GRCh38/hg38 1p31.1-22.2(chr1:76419302-88628464)x1 copy number loss See cases [RCV000138957] Chr1:76419302..88628464 [GRCh38]
Chr1:76884987..89094147 [GRCh37]
Chr1:76657575..88866735 [NCBI36]
Chr1:1p31.1-22.2
pathogenic
GRCh38/hg38 1p32.1-22.3(chr1:58819605-86098611)x1 copy number loss See cases [RCV000136913] Chr1:58819605..86098611 [GRCh38]
Chr1:59285277..86564294 [GRCh37]
Chr1:59057865..86336882 [NCBI36]
Chr1:1p32.1-22.3
pathogenic
GRCh38/hg38 1p31.1-13.3(chr1:72661709-107456880)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051825]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051825]|See cases [RCV000051825] Chr1:72661709..107456880 [GRCh38]
Chr1:73127392..107999502 [GRCh37]
Chr1:72899980..107801025 [NCBI36]
Chr1:1p31.1-13.3
pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:463
Count of miRNA genes:222
Interacting mature miRNAs:227
Transcripts:ENST00000413975, ENST00000417565, ENST00000417975, ENST00000419733, ENST00000457273
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.


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 1 1 1 1
Low 12 36 566 117 71 111 104 2 37 16 515 460 9 1 72 2 2
Below cutoff 1758 2373 1118 474 985 319 3390 1377 3211 343 786 982 163 1011 2104 3

Sequence


RefSeq Acc Id: ENST00000413975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,831,621 - 83,861,031 (-)Ensembl
RefSeq Acc Id: ENST00000417565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,831,621 - 83,860,943 (-)Ensembl
RefSeq Acc Id: ENST00000417975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,575,776 - 83,860,996 (-)Ensembl
RefSeq Acc Id: ENST00000419733
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,831,621 - 83,861,023 (-)Ensembl
RefSeq Acc Id: ENST00000457273
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,801,516 - 83,860,546 (-)Ensembl
RefSeq Acc Id: ENST00000657125
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,842,497 - 83,861,016 (-)Ensembl
RefSeq Acc Id: ENST00000662803
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,747,054 - 83,752,515 (-)Ensembl
RefSeq Acc Id: ENST00000670031
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,745,318 - 83,861,024 (-)Ensembl
RefSeq Acc Id: ENST00000685925
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,735,501 - 83,861,018 (-)Ensembl
RefSeq Acc Id: ENST00000688380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,747,383 - 83,861,038 (-)Ensembl
RefSeq Acc Id: ENST00000688565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,802,582 - 83,861,016 (-)Ensembl
RefSeq Acc Id: ENST00000689046
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,746,147 - 83,861,053 (-)Ensembl
RefSeq Acc Id: ENST00000689600
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,844,375 - 83,861,026 (-)Ensembl
RefSeq Acc Id: ENST00000701060
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,735,501 - 83,861,038 (-)Ensembl
RefSeq Acc Id: ENST00000701853
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,616,044 - 83,861,038 (-)Ensembl
RefSeq Acc Id: ENST00000701862
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,616,053 - 83,860,992 (-)Ensembl
RefSeq Acc Id: ENST00000702837
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,860,387 - 83,861,016 (-)Ensembl
RefSeq Acc Id: ENST00000702881
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl183,735,501 - 83,861,038 (-)Ensembl
RefSeq Acc Id: NR_119374
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38183,801,516 - 83,860,546 (-)NCBI
T2T-CHM13v2.0183,641,830 - 83,700,893 (-)NCBI
Sequence:

Additional Information

Database Acc Id Source(s)
COSMIC LINC01725 COSMIC
Ensembl Genes ENSG00000233008 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000457273 ENTREZGENE
GTEx ENSG00000233008 GTEx
Human Proteome Map LINC01725 Human Proteome Map
NCBI Gene LOC101927560 ENTREZGENE
RNAcentral URS000057EC58 RNACentral