KLC2 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "KLC2" in English language version.

refsWebsite

Global rank English rank

11nih.gov

4^th place

6doi.org

2^nd place

2ensembl.org

1,626^th place

1,007^th place

1omim.org

4,380^th place

4,305^th place

1rarediseases.org

5,181^st place

3,260^th place

1semanticscholar.org

11^th place

8^th place

1worldcat.org

5^th place

1handle.net

102^nd place

76^th place

doi.org (Global: 2^nd place; English: 2^nd place)

Rahman A, Friedman DS, Goldstein LS (Jun 1998). "Two kinesin light chain genes in mice. Identification and characterization of the encoded proteins". The Journal of Biological Chemistry. 273 (25): 15395–15403. doi:10.1074/jbc.273.25.15395. PMID 9624122.
Bowman AB, Kamal A, Ritchings BW, Philp AV, McGrail M, Gindhart JG, et al. (Nov 2000). "Kinesin-dependent axonal transport is mediated by the sunday driver (SYD) protein". Cell. 103 (4): 583–594. doi:10.1016/S0092-8674(00)00162-8. PMID 11106729. S2CID 247102.
Rahman A, Kamal A, Roberts EA, Goldstein LS (Sep 1999). "Defective kinesin heavy chain behavior in mouse kinesin light chain mutants". The Journal of Cell Biology. 146 (6): 1277–1288. doi:10.1083/jcb.146.6.1277. PMC 2156125. PMID 10491391.
Kok F, Weller M, de Paiva FR, Otto PA, Santos S (April 2010). "Inbreeding levels in Northeast Brazil: Strategies for the prospecting of new genetic disorders". Genetics and Molecular Biology. 33 (2): 220–223. doi:10.1590/S1415-47572010005000020. ISSN 1678-4685. PMC 3036858. PMID 21637472.
Melo US, Macedo-Souza LI, Figueiredo T, Muotri AR, Gleeson JG, Coux G, et al. (18 September 2015). "Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome". Human Molecular Genetics ddv388. doi:10.1093/hmg/ddv388. hdl:11336/29433. PMC 6296331.
Farias AA, Nunes K, Lemes RB, Moura R, Fernandes GR, Melo US, et al. (8 November 2018). "Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations". Scientific Reports. 8 (1) 16552. doi:10.1038/s41598-018-35022-1. PMC 6224410.

ensembl.org (Global: 1,626^th place; English: 1,007^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000174996 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000024862 – Ensembl, May 2017

handle.net (Global: 102^nd place; English: 76^th place)

hdl.handle.net

Melo US, Macedo-Souza LI, Figueiredo T, Muotri AR, Gleeson JG, Coux G, et al. (18 September 2015). "Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome". Human Molecular Genetics ddv388. doi:10.1093/hmg/ddv388. hdl:11336/29433. PMC 6296331.

nih.gov (Global: 4^th place; English: 4^th place)

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: KLC2 kinesin light chain 2".
Rahman A, Kamal A, Roberts EA, Goldstein LS (Sep 1999). "Defective kinesin heavy chain behavior in mouse kinesin light chain mutants". The Journal of Cell Biology. 146 (6): 1277–1288. doi:10.1083/jcb.146.6.1277. PMC 2156125. PMID 10491391.
Kok F, Weller M, de Paiva FR, Otto PA, Santos S (April 2010). "Inbreeding levels in Northeast Brazil: Strategies for the prospecting of new genetic disorders". Genetics and Molecular Biology. 33 (2): 220–223. doi:10.1590/S1415-47572010005000020. ISSN 1678-4685. PMC 3036858. PMID 21637472.
Melo US, Macedo-Souza LI, Figueiredo T, Muotri AR, Gleeson JG, Coux G, et al. (18 September 2015). "Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome". Human Molecular Genetics ddv388. doi:10.1093/hmg/ddv388. hdl:11336/29433. PMC 6296331.
Farias AA, Nunes K, Lemes RB, Moura R, Fernandes GR, Melo US, et al. (8 November 2018). "Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations". Scientific Reports. 8 (1) 16552. doi:10.1038/s41598-018-35022-1. PMC 6224410.

pubmed.ncbi.nlm.nih.gov

Rahman A, Friedman DS, Goldstein LS (Jun 1998). "Two kinesin light chain genes in mice. Identification and characterization of the encoded proteins". The Journal of Biological Chemistry. 273 (25): 15395–15403. doi:10.1074/jbc.273.25.15395. PMID 9624122.
Bowman AB, Kamal A, Ritchings BW, Philp AV, McGrail M, Gindhart JG, et al. (Nov 2000). "Kinesin-dependent axonal transport is mediated by the sunday driver (SYD) protein". Cell. 103 (4): 583–594. doi:10.1016/S0092-8674(00)00162-8. PMID 11106729. S2CID 247102.
Rahman A, Kamal A, Roberts EA, Goldstein LS (Sep 1999). "Defective kinesin heavy chain behavior in mouse kinesin light chain mutants". The Journal of Cell Biology. 146 (6): 1277–1288. doi:10.1083/jcb.146.6.1277. PMC 2156125. PMID 10491391.
Kok F, Weller M, de Paiva FR, Otto PA, Santos S (April 2010). "Inbreeding levels in Northeast Brazil: Strategies for the prospecting of new genetic disorders". Genetics and Molecular Biology. 33 (2): 220–223. doi:10.1590/S1415-47572010005000020. ISSN 1678-4685. PMC 3036858. PMID 21637472.

omim.org (Global: 4,380^th place; English: 4,305^th place)

"Entry - #609541 - SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN - OMIM". omim.org. Retrieved 2025-05-12.

rarediseases.org (Global: 5,181^st place; English: 3,260^th place)

"SPOAN syndrome - National Organization for Rare Disorders". rarediseases.org. Retrieved 2025-05-12.

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Bowman AB, Kamal A, Ritchings BW, Philp AV, McGrail M, Gindhart JG, et al. (Nov 2000). "Kinesin-dependent axonal transport is mediated by the sunday driver (SYD) protein". Cell. 103 (4): 583–594. doi:10.1016/S0092-8674(00)00162-8. PMID 11106729. S2CID 247102.

worldcat.org (Global: 5^th place; English: 5^th place)

search.worldcat.org

Kok F, Weller M, de Paiva FR, Otto PA, Santos S (April 2010). "Inbreeding levels in Northeast Brazil: Strategies for the prospecting of new genetic disorders". Genetics and Molecular Biology. 33 (2): 220–223. doi:10.1590/S1415-47572010005000020. ISSN 1678-4685. PMC 3036858. PMID 21637472.

KLC2 (English Wikipedia)

doi.org (Global: 2nd place; English: 2nd place)

ensembl.org (Global: 1,626th place; English: 1,007th place)