Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases
Descripción del Articulo
KIF1A is a molecular motor for membrane-bound cargo important to the development and survival of sensory neurons. KIF1A dysfunction has been associated with several Mendelian disorders with a spectrum of overlapping phenotypes, ranging from spastic paraplegia to intellectual disability. We present a...
| Autores: | , , , , , , , , , , , , , , , , , , , , , , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2020 |
| Institución: | Universidad Peruana de Ciencias Aplicadas |
| Repositorio: | UPC-Institucional |
| Lenguaje: | inglés |
| OAI Identifier: | oai:repositorioacademico.upc.edu.pe:10757/655505 |
| Enlace del recurso: | http://hdl.handle.net/10757/655505 |
| Nivel de acceso: | acceso embargado |
| Materia: | data lake genocentric germline mosaicism in-frame deletion KIF1A literature review |
| id |
UUPC_4ffd283acb6145104091b1528fb70d13 |
|---|---|
| oai_identifier_str |
oai:repositorioacademico.upc.edu.pe:10757/655505 |
| network_acronym_str |
UUPC |
| network_name_str |
UPC-Institucional |
| repository_id_str |
2670 |
| dc.title.en_US.fl_str_mv |
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases |
| title |
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases |
| spellingShingle |
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases Montenegro-Garreaud, Ximena data lake genocentric germline mosaicism in-frame deletion KIF1A literature review |
| title_short |
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases |
| title_full |
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases |
| title_fullStr |
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases |
| title_full_unstemmed |
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases |
| title_sort |
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases |
| author |
Montenegro-Garreaud, Ximena |
| author_facet |
Montenegro-Garreaud, Ximena Hansen, Adam W. Khayat, Michael M. Chander, Varuna Grochowski, Christopher M. Jiang, Yunyun Li, He Mitani, Tadahiro Kessler, Elena Jayaseelan, Joy Shen, Hua Gezdirici, Alper Pehlivan, Davut Meng, Qingchang Rosenfeld, Jill A. Jhangiani, Shalini N. Madan-Khetarpal, Suneeta Scott, Daryl A. Abarca-Barriga, Hugo Trubnykova, Milana Gingras, Marie Claude Muzny, Donna M. Posey, Jennifer E. Liu, Pengfei Lupski, James R. Gibbs, Richard A. |
| author_role |
author |
| author2 |
Hansen, Adam W. Khayat, Michael M. Chander, Varuna Grochowski, Christopher M. Jiang, Yunyun Li, He Mitani, Tadahiro Kessler, Elena Jayaseelan, Joy Shen, Hua Gezdirici, Alper Pehlivan, Davut Meng, Qingchang Rosenfeld, Jill A. Jhangiani, Shalini N. Madan-Khetarpal, Suneeta Scott, Daryl A. Abarca-Barriga, Hugo Trubnykova, Milana Gingras, Marie Claude Muzny, Donna M. Posey, Jennifer E. Liu, Pengfei Lupski, James R. Gibbs, Richard A. |
| author2_role |
author author author author author author author author author author author author author author author author author author author author author author author author author |
| dc.contributor.author.fl_str_mv |
Montenegro-Garreaud, Ximena Hansen, Adam W. Khayat, Michael M. Chander, Varuna Grochowski, Christopher M. Jiang, Yunyun Li, He Mitani, Tadahiro Kessler, Elena Jayaseelan, Joy Shen, Hua Gezdirici, Alper Pehlivan, Davut Meng, Qingchang Rosenfeld, Jill A. Jhangiani, Shalini N. Madan-Khetarpal, Suneeta Scott, Daryl A. Abarca-Barriga, Hugo Trubnykova, Milana Gingras, Marie Claude Muzny, Donna M. Posey, Jennifer E. Liu, Pengfei Lupski, James R. Gibbs, Richard A. |
| dc.subject.en_US.fl_str_mv |
data lake genocentric germline mosaicism in-frame deletion KIF1A literature review |
| topic |
data lake genocentric germline mosaicism in-frame deletion KIF1A literature review |
| description |
KIF1A is a molecular motor for membrane-bound cargo important to the development and survival of sensory neurons. KIF1A dysfunction has been associated with several Mendelian disorders with a spectrum of overlapping phenotypes, ranging from spastic paraplegia to intellectual disability. We present a novel pathogenic in-frame deletion in the KIF1A molecular motor domain inherited by two affected siblings from an unaffected mother with apparent germline mosaicism. We identified eight additional cases with heterozygous, pathogenic KIF1A variants ascertained from a local data lake. Our data provide evidence for the expansion of KIF1A-associated phenotypes to include hip subluxation and dystonia as well as phenotypes observed in only a single case: gelastic cataplexy, coxa valga, and double collecting system. We review the literature and suggest that KIF1A dysfunction is better understood as a single neuromuscular disorder with variable involvement of other organ systems than a set of discrete disorders converging at a single locus. |
| publishDate |
2020 |
| dc.date.accessioned.none.fl_str_mv |
2021-04-14T12:28:39Z |
| dc.date.available.none.fl_str_mv |
2021-04-14T12:28:39Z |
| dc.date.issued.fl_str_mv |
2020-12-01 |
| dc.type.en_US.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.issn.none.fl_str_mv |
10597794 |
| dc.identifier.doi.none.fl_str_mv |
10.1002/humu.24118 |
| dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/10757/655505 |
| dc.identifier.eissn.none.fl_str_mv |
10981004 |
| dc.identifier.journal.en_US.fl_str_mv |
Human Mutation |
| dc.identifier.eid.none.fl_str_mv |
2-s2.0-85092158304 |
| dc.identifier.scopusid.none.fl_str_mv |
SCOPUS_ID:85092158304 |
| dc.identifier.isni.none.fl_str_mv |
0000 0001 2196 144X |
| identifier_str_mv |
10597794 10.1002/humu.24118 10981004 Human Mutation 2-s2.0-85092158304 SCOPUS_ID:85092158304 0000 0001 2196 144X |
| url |
http://hdl.handle.net/10757/655505 |
| dc.language.iso.en_US.fl_str_mv |
eng |
| language |
eng |
| dc.relation.url.en_US.fl_str_mv |
https://onlinelibrary.wiley.com/doi/10.1002/humu.24118 |
| dc.rights.en_US.fl_str_mv |
info:eu-repo/semantics/embargoedAccess |
| eu_rights_str_mv |
embargoedAccess |
| dc.format.en_US.fl_str_mv |
application/pdf |
| dc.publisher.en_US.fl_str_mv |
John Wiley and Sons Inc |
| dc.source.es_PE.fl_str_mv |
Universidad Peruana de Ciencias Aplicadas (UPC) Repositorio Academico - UPC |
| dc.source.none.fl_str_mv |
reponame:UPC-Institucional instname:Universidad Peruana de Ciencias Aplicadas instacron:UPC |
| instname_str |
Universidad Peruana de Ciencias Aplicadas |
| instacron_str |
UPC |
| institution |
UPC |
| reponame_str |
UPC-Institucional |
| collection |
UPC-Institucional |
| dc.source.journaltitle.none.fl_str_mv |
Human Mutation |
| dc.source.volume.none.fl_str_mv |
41 |
| dc.source.issue.none.fl_str_mv |
12 |
| dc.source.beginpage.none.fl_str_mv |
2094 |
| dc.source.endpage.none.fl_str_mv |
2104 |
| bitstream.url.fl_str_mv |
https://repositorioacademico.upc.edu.pe/bitstream/10757/655505/1/license.txt |
| bitstream.checksum.fl_str_mv |
8a4605be74aa9ea9d79846c1fba20a33 |
| bitstream.checksumAlgorithm.fl_str_mv |
MD5 |
| repository.name.fl_str_mv |
Repositorio académico upc |
| repository.mail.fl_str_mv |
upc@openrepository.com |
| _version_ |
1846065751368138752 |
| spelling |
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-Garreaud, XimenaHansen, Adam W.Khayat, Michael M.Chander, VarunaGrochowski, Christopher M.Jiang, YunyunLi, HeMitani, TadahiroKessler, ElenaJayaseelan, JoyShen, HuaGezdirici, AlperPehlivan, DavutMeng, QingchangRosenfeld, Jill A.Jhangiani, Shalini N.Madan-Khetarpal, SuneetaScott, Daryl A.Abarca-Barriga, HugoTrubnykova, MilanaGingras, Marie ClaudeMuzny, Donna M.Posey, Jennifer E.Liu, PengfeiLupski, James R.Gibbs, Richard A.2021-04-14T12:28:39Z2021-04-14T12:28:39Z2020-12-011059779410.1002/humu.24118http://hdl.handle.net/10757/65550510981004Human Mutation2-s2.0-85092158304SCOPUS_ID:850921583040000 0001 2196 144XKIF1A is a molecular motor for membrane-bound cargo important to the development and survival of sensory neurons. KIF1A dysfunction has been associated with several Mendelian disorders with a spectrum of overlapping phenotypes, ranging from spastic paraplegia to intellectual disability. We present a novel pathogenic in-frame deletion in the KIF1A molecular motor domain inherited by two affected siblings from an unaffected mother with apparent germline mosaicism. We identified eight additional cases with heterozygous, pathogenic KIF1A variants ascertained from a local data lake. Our data provide evidence for the expansion of KIF1A-associated phenotypes to include hip subluxation and dystonia as well as phenotypes observed in only a single case: gelastic cataplexy, coxa valga, and double collecting system. We review the literature and suggest that KIF1A dysfunction is better understood as a single neuromuscular disorder with variable involvement of other organ systems than a set of discrete disorders converging at a single locus.National Institutes of HealthRevisión por paresapplication/pdfengJohn Wiley and Sons Inchttps://onlinelibrary.wiley.com/doi/10.1002/humu.24118info:eu-repo/semantics/embargoedAccessUniversidad Peruana de Ciencias Aplicadas (UPC)Repositorio Academico - UPCHuman Mutation411220942104reponame:UPC-Institucionalinstname:Universidad Peruana de Ciencias Aplicadasinstacron:UPCdata lakegenocentricgermline mosaicismin-frame deletionKIF1Aliterature reviewPhenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published casesinfo:eu-repo/semantics/articleLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorioacademico.upc.edu.pe/bitstream/10757/655505/1/license.txt8a4605be74aa9ea9d79846c1fba20a33MD51false10757/655505oai:repositorioacademico.upc.edu.pe:10757/6555052021-04-14 12:28:39.905Repositorio académico upcupc@openrepository.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 |
| score |
13.888049 |
Nota importante:
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).