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Gene: LOC105376695 (uncharacterized LOC105376695) Homo sapiens

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Symbol:

LOC105376695

Name:

uncharacterized LOC105376695

RGD ID:

38640241

Description:

Type:

ncrna

RefSeq Status:

MODEL

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	1	8,239,958 - 8,249,007 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
Cytogenetic Map	1	p36.23	NCBI
CHM1_1	1	8,288,169 - 8,296,730 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	1	7,770,987 - 7,780,039 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1298451	OSTEAR17_H	Osteoarthritis QTL 17 (human)	2.4	0.0004	Joint/bone inflammation	osteoarthritis	11	1	25188105	Human
1576329	MYI9_H	Myocardial infarction susceptibility QTL 9 (human)	12		Myocardial infarction susceptibility	early-onset	1	7585503	33585503	Human
1298463	BP9_H	Blood pressure QTL 9 (human)	3.9		Blood pressure	hypertension susceptibility	1	1	25188105	Human
1576325	MYI1_H	Myocardial infarction susceptibility QTL 1 (human)	11.68	1e-12	Myocardial infarction susceptibility	early-onset	1	7585503	33585503	Human
1643380	BW316_H	Body weight QTL 316 (human)	2.62	0.0002	Body weight	BMI	1	7585503	33585503	Human

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.


RefSeq Transcripts	XR_007069840	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_946937	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AL358876	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068277	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

XR_007069840

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	7,770,987 - 7,780,039 (+)	NCBI

RefSeq Acc Id:

XR_946937

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	8,239,958 - 8,249,007 (+)	NCBI

Sequence:

show sequence

CCGGCCTCAGCCCCCCGAGCAGCTGGGAATACAGGAGAAATTAAATATCAGAGTTGGAAAGGACAGAAGCAGCCTGAACTCTCATCCATATGAACTCTGTACAACCATTGTGGAGGGCCATTGGCAGT
ACACAGTCAAGTTGAAGACGGAGTCTTGCTGTGTCGCCCAGGCGGGAG

hide sequence

Database	Acc Id	Source(s)
COSMIC	LOC105376695	COSMIC
Ensembl Genes	ENSG00000298156	ENTREZGENE
Ensembl Transcript	ENST00000753408	ENTREZGENE
GTEx	ENSG00000298156	GTEx
Human Proteome Map	LOC105376695	Human Proteome Map
NCBI Gene	LOC105376695	ENTREZGENE

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailable


InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailable


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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