LARP4 La ribonucleoprotein 4

Go to:

Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
Genome browser

Information

Symbol: LARP4
Type: protein-coding
Description: La ribonucleoprotein 4
Entrez Gene ID: 113251
Genome: hg19
Position: chr12:50,794,640-50,871,300
Genome: hg38
Position: chr12:50,400,857-50,477,517
MIM: 618657 OMIM
HGNC: HGNC:24320 HGNC
Ensembl: ENSG00000161813 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
Uncertain significance	0	58

Ranking

	ClinVar
	0
	0
	0
	60
	0

Frequency

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

Disease area statistics

[No Data.]

Locus Zoom

Variants

Search Word

Target data	:	MGeND data only
Category	:
Search word	:
Filtering	:

Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	MGeND				Genome	ClinVar			CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

Search Word

Target data	:	MGeND data only
Category	:
Search word	:
Filtering	:

Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
Category	:
Search word	:
Filtering	:

Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	PP13296
MIM	618657 OMIM
HGNC	HGNC:24320 HGNC
Ensembl	ENSG00000161813 Ensembl
AllianceGenome	HGNC:24320

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000293618.12	hg38	chr12	50,400,809	50,479,996	79,188
ENST00000518561.5	hg38	chr12	50,400,956	50,461,487	60,532
ENST00000347328.9	hg38	chr12	50,400,985	50,477,497	76,513
ENST00000518444.5	hg38	chr12	50,400,929	50,476,463	75,535
ENST00000429001.7	hg38	chr12	50,400,857	50,477,517	76,661
ENST00000398473.7	hg38	chr12	50,400,885	50,480,004	79,120
ENST00000522085.5	hg38	chr12	50,400,908	50,461,487	60,580
ENST00000293618.12	hg19	chr12	50,794,592	50,873,779	79,188
ENST00000429001.7	hg19	chr12	50,794,640	50,871,300	76,661
ENST00000398473.7	hg19	chr12	50,794,668	50,873,787	79,120
ENST00000518444.5	hg19	chr12	50,794,712	50,870,246	75,535
ENST00000347328.9	hg19	chr12	50,794,768	50,871,280	76,513
ENST00000518561.5	hg19	chr12	50,794,739	50,855,270	60,532
ENST00000522085.5	hg19	chr12	50,794,691	50,855,270	60,580

Key	Value
strand	+
start	50,794,591
Gene Symbol	LARP4
Entrez GeneId	113,251
Chr Band	12q13.12
end	50,873,787
chr	chr12

Genome browser