(Q37342031)

19 August 2017

Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes (English)

1 reference

19 August 2017

Belphegor Dmel_CG6815

1 reference

GOA release 2020-03-11

1 reference

1 reference

16

1 reference

19 August 2017

38

Eric Boerwinkle

0 references

Jennifer E. Posey

Jennifer E Posey

7

0 references

Brett H Graham

Brett H Graham

43

0 references

Massimo Zeviani

30

Massimo Zeviani

1 reference

19 August 2017

20

Costanza Lamperti

1 reference

University of Washington Center for Mendelian Genomics

19 August 2017

40

University of Washington Center for Mendelian Genomics

1 reference

19 August 2017

50

James R Lupski

1 reference

19 August 2017

41

Richard A Gibbs

1 reference

19 August 2017

36

Donna M Muzny

1 reference

19 August 2017

24

Christine M Eng

1 reference

19 August 2017

44

Yaping Yang

1 reference

19 August 2017

27

Tommaso Pippucci

1 reference

19 August 2017

2

Wan Hee Yoon

1 reference

19 August 2017

9

Jill A Rosenfeld

1 reference

19 August 2017

1

Tamar Harel

1 reference

19 August 2017

14

Theodore Chiang

1 reference

19 August 2017

6

Mohammad K Eldomery

1 reference

19 August 2017

Baylor-Hopkins Center for Mendelian Genomics

39

Baylor-Hopkins Center for Mendelian Genomics

1 reference

19 August 2017

18

Yunru Shao

1 reference

19 August 2017

Caterina Garone

3

1 reference

19 August 2017

Shen Gu

4

1 reference

19 August 2017

Zeynep Coban-Akdemir

5

1 reference

19 August 2017

Shalini N Jhangiani

8

1 reference

19 August 2017

Megan T Cho

10

1 reference

19 August 2017

Stephanie Fox

11

1 reference

19 August 2017

Marjorie Withers

12

1 reference

19 August 2017

Stephanie M Brooks

13

1 reference

19 August 2017

Lita Duraine

15

1 reference

19 August 2017

Bo Yuan

17

1 reference

19 August 2017

Elie Moussallem

19

1 reference

19 August 2017

Maria A Donati

21

1 reference

19 August 2017

Joshua D Smith

22

1 reference

19 August 2017

Heather M McLaughlin

23

1 reference

19 August 2017

Magdalena Walkiewicz

25

1 reference

19 August 2017

Fan Xia

26

1 reference

19 August 2017

Pamela Magini

28

1 reference

19 August 2017

Marco Seri

29

1 reference

19 August 2017

Michio Hirano

31

1 reference

19 August 2017

Jill V Hunter

32

1 reference

19 August 2017

Myriam Srour

33

1 reference

19 August 2017

Stefano Zanigni

34

1 reference

19 August 2017

Richard Alan Lewis

35

1 reference

19 August 2017

Timothy E Lotze

37

1 reference

19 August 2017

Scott E Hickey

42

1 reference

19 August 2017

Daniela Buhas

45

1 reference

19 August 2017

Donna M Martin

46

1 reference

19 August 2017

Lorraine Potocki

47

1 reference

19 August 2017

Claudio Graziano

48

1 reference

19 August 2017

Hugo J Bellen

49

1 reference

19 August 2017

language of work or name

English

0 references

publication date

7 September 2016

1 reference

American Journal of Human Genetics

19 August 2017

1 reference

19 August 2017

99

1 reference

19 August 2017

4

1 reference

19 August 2017

831-845

1 reference

describes a project that uses

19 August 2017

PyMOL

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=pmc&rettype=xml&id=PMC5065660

cites work

Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy

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Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila

6 September 2017

1 reference

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Mechanisms underlying structural variant formation in genomic disorders

6 September 2017

1 reference

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Molecular diagnostic experience of whole-exome sequencing in adult patients

6 September 2017

1 reference

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Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation

6 September 2017

1 reference

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Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

6 September 2017

1 reference

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Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission

6 September 2017

1 reference

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Somatic mosaicism: implications for disease and transmission genetics

6 September 2017

1 reference

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Mitochondrial dynamics and inherited peripheral nerve diseases.

6 September 2017

1 reference

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Mitochondrial ATAD3A combines with GRP78 to regulate the WASF3 metastasis-promoting protein

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defect

6 September 2017

1 reference

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De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

The I-TASSER Suite: protein structure and function prediction.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

A high-resolution copy-number variation resource for clinical and population genetics

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

6 September 2017

1 reference

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Mitochondria-associated membrane formation in hormone-stimulated Leydig cell steroidogenesis: role of ATAD3.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Molecular findings among patients referred for clinical whole-exome sequencing

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Parent of origin, mosaicism, and recurrence risk: probabilistic modeling explains the broken symmetry of transmission genetics

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Mitochondrial dynamics and inheritance during cell division, development and disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Expression analysis of ATAD3 isoforms in rodent and human cell lines and tissues.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Clinical whole-exome sequencing for the diagnosis of mendelian disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Mitochondrial protein ATPase family, AAA domain containing 3A correlates with radioresistance in glioblastoma

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Atad3 function is essential for early post-implantation development in the mouse

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Identification of a dynamic mitochondrial protein complex driving cholesterol import, trafficking, and metabolism to steroid hormones

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

ATAD3B is a human embryonic stem cell specific mitochondrial protein, re-expressed in cancer cells, that functions as dominant negative for the ubiquitous ATAD3A.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Mitochondrial nucleoid interacting proteins support mitochondrial protein synthesis.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

An integrative variant analysis suite for whole exome next-generation sequencing data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

A copy number variation morbidity map of developmental delay

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

ConSurf 2010: calculating evolutionary conservation in sequence and structure of proteins and nucleic acids

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

ATPase family AAA domain-containing 3A is a novel anti-apoptotic factor in lung adenocarcinoma cells

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Multi-system neurological disease is common in patients with OPA1 mutations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

The AAA+ ATPase ATAD3A controls mitochondrial dynamics at the interface of the inner and outer membranes.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

C. elegans ATAD-3 is essential for mitochondrial activity and development

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

The Sequence Alignment/Map format and SAMtools

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

I-TASSER server for protein 3D structure prediction

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

An optimized transgenesis system for Drosophila using germ-line-specific phiC31 integrases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

P[acman]: a BAC transgenic platform for targeted insertion of large DNA fragments in D. melanogaster.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

AAA proteases of mitochondria: quality control of membrane proteins and regulatory functions during mitochondrial biogenesis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Molecular basis of base substitution hotspots in Escherichia coli

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

GeneMatcher: a matching tool for connecting investigators with an interest in the same gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

GDAP1 mutations differ in their effects on mitochondrial dynamics and apoptosis depending on the mode of inheritance.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides, as well as in CpG dinucleotides

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

A lethal defect of mitochondrial and peroxisomal fission

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Miropeats: graphical DNA sequence comparisons

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Retraction for Li et al., "ATAD3 Is a Limiting Factor in Mitochondrial Biogenesis and Adipogenesis of White Adipocyte-Like 3T3-L1 Cells".

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Mutation rates in the dystrophin gene: a hotspot of mutation at a CpG dinucleotide

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Clinical and molecular findings in children with complex I deficiency

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5065660

10.1016/J.AJHG.2016.08.007

2 September 2018

Identifiers

DOI

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

27640307

1 reference