DisGeNET - a database of gene-disease associations

MSTO1, misato mitochondrial distribution and morphology regulator 1, 55154

N. diseases: 124; N. variants: 6

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C0740279
Disease:

Cerebellar atrophy

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C0575081
Disease:

Gait abnormality

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C0454642
Disease:

Receptive language delay

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C0520966
Disease:

Abnormal coordination

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C1836479
Disease:

Saccadic smooth pursuit

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C1836696
Disease:

Lower limb hyperreflexia

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C0427190
Disease:

Ataxia, Truncal

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C3714796
Disease:

Isolated somatotropin deficiency

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C0234518
Disease:

Slurred speech

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs749922789

rs749922789

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C4540096
Disease:

MYOPATHY, MITOCHONDRIAL, AND ATAXIA

0.700

GeneticVariation

UNIPROT

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C4540096
Disease:

MYOPATHY, MITOCHONDRIAL, AND ATAXIA

0.800

GeneticVariation

UNIPROT

dbSNP:

rs622288

rs622288

Entrez Id:	55154;105371452
Gene Symbol:	MSTO1;LOC105371452

MSTO1;LOC105371452

CUI:	C4540096
Disease:

MYOPATHY, MITOCHONDRIAL, AND ATAXIA

T

0.800

GeneticVariation

CLINVAR