SRRT serrate, RNA effector molecule

Go to:

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

Information

Symbol: SRRT
Type: protein-coding
Description: serrate, RNA effector molecule
Entrez Gene ID: 51593
Genome: hg19
Position: chr7:100,472,725-100,486,285
Genome: hg38
Position: chr7:100,875,103-100,888,664
MIM: 614469 OMIM
HGNC: HGNC:24101 HGNC
Ensembl: ENSG00000087087 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	16
Likely benign	0	6
Uncertain significance	0	66

Ranking

	ClinVar
	0
	0
	0
	88
	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	ARS2
SYNONYM	ASR2
SYNONYM	serrate
MIM	614469 OMIM
HGNC	HGNC:24101 HGNC
Ensembl	ENSG00000087087 Ensembl
AllianceGenome	HGNC:24101

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000614484.4	hg38	chr7	100,875,126	100,888,664	13,539
ENST00000618411.4	hg38	chr7	100,875,185	100,888,664	13,480
ENST00000611405.5	hg38	chr7	100,875,103	100,888,664	13,562
ENST00000618262.4	hg38	chr7	100,875,126	100,888,664	13,539
ENST00000611405.5	hg19	chr7	100,472,725	100,486,285	13,561
ENST00000618262.4	hg19	chr7	100,472,748	100,486,285	13,538
ENST00000614484.4	hg19	chr7	100,472,748	100,486,285	13,538
ENST00000618411.4	hg19	chr7	100,472,807	100,486,285	13,479

Genome browser