MID1IP1 MID1 interacting protein 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: MID1IP1
Type: protein-coding
Description: MID1 interacting protein 1
Entrez Gene ID: 58526
Genome: hg19
Position: chrX:38,660,708-38,665,790
Genome: hg38
Position: chrX:38,801,455-38,806,537
MIM: 300961 OMIM
HGNC: HGNC:20715 HGNC
Ensembl: ENSG00000165175 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	6
not provided	6	0
Uncertain significance	0	8

Ranking

	ClinVar
	0
	0
	0
	14
	2

Frequency

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

Disease area statistics

Locus Zoom

Variants

Search Word

Target data	:	MGeND data only
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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
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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	:
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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	G12-like
SYNONYM	MIG12
SYNONYM	S14R
SYNONYM	STRAIT11499
SYNONYM	THRSPL
MIM	300961 OMIM
HGNC	HGNC:20715 HGNC
Ensembl	ENSG00000165175 Ensembl
AllianceGenome	HGNC:20715

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000336949.7	hg38	chrX	38,801,455	38,806,537	5,083
ENST00000614558.3	hg38	chrX	38,801,459	38,806,532	5,074
ENST00000378474.3	hg38	chrX	38,801,454	38,806,433	4,980
ENST00000457894.5	hg38	chrX	38,801,440	38,806,446	5,007
ENST00000457894.5	hg19	chrX	38,660,693	38,665,699	5,007
ENST00000378474.3	hg19	chrX	38,660,707	38,665,686	4,980
ENST00000336949.7	hg19	chrX	38,660,708	38,665,790	5,083
ENST00000614558.3	hg19	chrX	38,660,712	38,665,785	5,074

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