KIFC3

From Wikipedia, the free encyclopedia

Kinesin family member C3

PDB rendering based on 2h58.

Available structures: 2h58

Identifiers

Symbol(s)

KIFC3; DKFZp686D23201

External IDs

OMIM: 604535 MGI: 109202 HomoloGene: 83229

Gene ontology
Molecular Function:	• nucleotide binding • microtubule motor activity • ATP binding
Cellular Component:	• Golgi apparatus • kinesin complex • microtubule
Biological Process:	• microtubule-based movement • Golgi organization and biogenesis • visual perception

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_005550 (mRNA)
NP_005541 (protein)

NM_010631 (mRNA)
NP_034761 (protein)

Location

Chr 16: 56.35 - 56.39 Mb

Chr 8: 97.99 - 98.03 Mb

Pubmed search

[1]

[2]

Kinesin family member C3, also known as KIFC3, is a human gene.^[1]

[edit] References

^ Entrez Gene: KIFC3 kinesin family member C3.

[edit] Further reading

Diu A, Moebius U, Ferradini L, et al. (1993). "Limited T-cell receptor diversity in liver-infiltrating lymphocytes from patients with primary biliary cirrhosis.". J. Autoimmun. 6 (5): 611-9. doi:10.1006/jaut.1993.1050. PMID 8240664.
Hoang EH, Whitehead JL, Dosé AC, Burnside B (1998). "Cloning of a novel C-terminal kinesin (KIFC3) that maps to human chromosome 16q13-q21 and thus is a candidate gene for Bardet-Biedl syndrome.". Genomics 52 (2): 219-22. doi:10.1006/geno.1998.5431. PMID 9782090.
Hoang E, Bost-Usinger L, Burnside B (1999). "Characterization of a novel C-kinesin (KIFC3) abundantly expressed in vertebrate retina and RPE.". Exp. Eye Res. 69 (1): 57-68. doi:10.1006/exer.1999.0671. PMID 10375449.
Noda Y, Okada Y, Saito N, et al. (2001). "KIFC3, a microtubule minus end-directed motor for the apical transport of annexin XIIIb-associated Triton-insoluble membranes.". J. Cell Biol. 155 (1): 77-88. doi:10.1083/jcb.200108042. PMID 11581287.
Xu Y, Takeda S, Nakata T, et al. (2002). "Role of KIFC3 motor protein in Golgi positioning and integration.". J. Cell Biol. 158 (2): 293-303. doi:10.1083/jcb.200202058. PMID 12135985.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi:10.1038/ng1285. PMID 14702039.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334.
Roni V, Carpio R, Wissinger B (2007). "Mapping of transcription start sites of human retina expressed genes.". BMC Genomics 8: 42. doi:10.1186/1471-2164-8-42. PMID 17286855.