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Liu, D. KIF1B Gene. Encyclopedia. Available online: (accessed on 24 April 2024).
Liu D. KIF1B Gene. Encyclopedia. Available at: Accessed April 24, 2024.
Liu, Dean. "KIF1B Gene" Encyclopedia, (accessed April 24, 2024).
Liu, D. (2020, December 23). KIF1B Gene. In Encyclopedia.
Liu, Dean. "KIF1B Gene." Encyclopedia. Web. 23 December, 2020.
KIF1B Gene

Kinesin family member 1B


1. Introduction

The KIF1B gene provides instructions for making a protein called kinesin family member 1B, part of the kinesin family of proteins. These proteins are essential for the transport of materials within cells. Kinesin proteins function like freight trains that transport cargo, and their structure is suited for this cargo-carrying function. One part of the protein, called the motor domain, provides the power to move the protein and its cargo along a track-like system made from structures called microtubules. Another part of the kinesin protein, which varies among members of this protein family, binds to specific materials for transport.

Research suggests that the kinesin family member 1B protein specializes in carrying two types of cargo. In nerve cells (neurons), this protein transports small, sac-like structures called synaptic vesicles, which contain materials necessary for the transmission of nerve impulses. In other cell types, the kinesin family member 1B protein carries energy-producing structures called mitochondria.

In addition to its transport functions, the kinesin family member 1B protein appears to be involved in programmed cell death (apoptosis). Apoptosis is a common process throughout life that helps the body get rid of cells it does not need.

2. Health Conditions Related to Genetic Changes

2.1. Neuroblastoma

Deletion of a region of chromosome 1 containing the KIF1B gene, designated 1p36, has been identified in some people with neuroblastoma, a type of cancerous tumor composed of immature nerve cells (neuroblasts). 1p36 deletions are somatic mutations, which means they occur during a person's lifetime and are present only in the cells that become cancerous. In addition, several inherited KIF1B gene mutations have been identified in families with a history of neuroblastoma. These mutations change single protein building blocks (amino acids) in the kinesin family member 1B protein. Studies suggest that deletion or mutation of the KIF1B gene may disrupt apoptosis, allowing cells to grow and divide too quickly or in an uncontrolled way. This kind of unregulated cell growth can lead to the formation of tumors.

2.2. Nonsyndromic Paraganglioma

KIF1B gene mutations have been reported in individuals with a type of paraganglioma called pheochromocytoma. Paragangliomas are noncancerous (benign) tumors of the nervous system. Pheochromocytomas specifically affect the adrenal glands, which are small hormone-producing glands located on top of each kidney. These tumors often cause no symptoms, but in some cases they can produce an excess of hormones that cause dangerously high blood pressure. KIF1B gene mutations are associated with nonsyndromic pheochromocytoma, which means the tumors occur without additional features of an inherited syndrome.

The KIF1B gene mutations identified in nonsyndromic pheochromocytoma change single amino acids in the kinesin family member 1B protein. Studies suggest that the mutations may disrupt apoptosis, allowing cells to grow and divide too quickly or in an uncontrolled way and potentially leading to tumor formation.

3. Other Names for This Gene

  • CMT2

  • CMT2A


  • KIAA0591

  • KIAA1488


  • KLP


  1. Berger P, Young P, Suter U. Molecular cell biology of Charcot-Marie-Toothdisease. Neurogenetics. 2002 Mar;4(1):1-15. Review.
  2. Galan SR, Kann PH. Genetics and molecular pathogenesis of pheochromocytoma andparaganglioma. Clin Endocrinol (Oxf). 2013 Feb;78(2):165-75. doi:10.1111/cen.12071. Review.
  3. Henrich KO, Schwab M, Westermann F. 1p36 tumor suppression--a matter ofdosage? Cancer Res. 2012 Dec 1;72(23):6079-88. doi:10.1158/0008-5472.CAN-12-2230.
  4. Munirajan AK, Ando K, Mukai A, Takahashi M, Suenaga Y, Ohira M, Koda T, HirotaT, Ozaki T, Nakagawara A. KIF1Bbeta functions as a haploinsufficient tumorsuppressor gene mapped to chromosome 1p36.2 by inducing apoptotic cell death. JBiol Chem. 2008 Sep 5;283(36):24426-34. doi: 10.1074/jbc.M802316200.
  5. Niemann A, Berger P, Suter U. Pathomechanisms of mutant proteins inCharcot-Marie-Tooth disease. Neuromolecular Med. 2006;8(1-2):217-42. Review.
  6. Qin Y, Buddavarapu K, Dahia PL. Pheochromocytomas: from genetic diversity tonew paradigms. Horm Metab Res. 2009 Sep;41(9):664-71. doi:10.1055/s-0029-1215590.
  7. Schlisio S, Kenchappa RS, Vredeveld LC, George RE, Stewart R, Greulich H,Shahriari K, Nguyen NV, Pigny P, Dahia PL, Pomeroy SL, Maris JM, Look AT,Meyerson M, Peeper DS, Carter BD, Kaelin WG Jr. The kinesin KIF1Bbeta actsdownstream from EglN3 to induce apoptosis and is a potential 1p36 tumorsuppressor. Genes Dev. 2008 Apr 1;22(7):884-93. doi: 10.1101/gad.1648608.
  8. Yeh IT, Lenci RE, Qin Y, Buddavarapu K, Ligon AH, Leteurtre E, Do Cao C,Cardot-Bauters C, Pigny P, Dahia PL. A germline mutation of the KIF1B beta geneon 1p36 in a family with neural and nonneural tumors. Hum Genet. 2008Oct;124(3):279-85. doi: 10.1007/s00439-008-0553-1.
  9. Zhao C, Takita J, Tanaka Y, Setou M, Nakagawa T, Takeda S, Yang HW, Terada S, Nakata T, Takei Y, Saito M, Tsuji S, Hayashi Y, Hirokawa N. Charcot-Marie-Toothdisease type 2A caused by mutation in a microtubule motor KIF1Bbeta. Cell. 2001Jun 1;105(5):587-97. Erratum in: Cell 2001 Jul 13;106(1):127.
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Update Date: 23 Dec 2020