RN7SL386P (RNA, 7SL, cytoplasmic 386, pseudogene) - Rat Genome Database

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Gene: RN7SL386P (RNA, 7SL, cytoplasmic 386, pseudogene) Homo sapiens
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Symbol: RN7SL386P
Name: RNA, 7SL, cytoplasmic 386, pseudogene
RGD ID: 10413203
HGNC Page HGNC:46402
Description:
Type: pseudo (Ensembl: misc_RNA)
RefSeq Status: INFERRED
Related Functional Gene: RN7SL1  
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38121,987,481 - 21,987,777 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl121,987,481 - 21,987,777 (+)EnsemblGRCh38hg38GRCh38
GRCh37122,313,974 - 22,314,270 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map1p36.12NCBI
CHM1_1122,426,513 - 22,426,808 (+)NCBICHM1_1
T2T-CHM13v2.0121,811,293 - 21,811,589 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


References

Genomics


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1298451OSTEAR17_HOsteoarthritis QTL 17 (human)2.40.0004Joint/bone inflammationosteoarthritis11125188105Human
1576329MYI9_HMyocardial infarction susceptibility QTL 9 (human)12Myocardial infarction susceptibilityearly-onset1758550333585503Human
1298463BP9_HBlood pressure QTL 9 (human)3.9Blood pressurehypertension susceptibility1125188105Human
1576325MYI1_HMyocardial infarction susceptibility QTL 1 (human)11.681e-12Myocardial infarction susceptibilityearly-onset1758550333585503Human
1643380BW316_HBody weight QTL 316 (human)2.620.0002Body weightBMI1758550333585503Human


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
sensory system
54 255 77 68 126 88 84 26 83 14 59 307 244 66 22 174 58 13

Sequence


Ensembl Acc Id: ENST00000485776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,987,481 - 21,987,777 (+)Ensembl

Additional Information

Database Acc Id Source(s)
COSMIC RN7SL386P COSMIC
Ensembl Genes ENSG00000273610 Ensembl, ENTREZGENE
GTEx ENSG00000273610 GTEx
HGNC ID HGNC:46402 ENTREZGENE
Human Proteome Map RN7SL386P Human Proteome Map
NCBI Gene RN7SL386P ENTREZGENE