Ir al contenido principal

kinesin family member 1B

El 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.

Normal function

El 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.

Conditions referring to this gene or chromosome

Otros nombres

CMT2

CMT2A

HMSNII

KIAA0591

KIAA1488

KIF1B_HUMAN

KLP

Related patient information and medicines

Enfermedad renal poliquística

Patient information leaflet

Enfermedad renal poliquística

Polycystic kidney disease (PKD) causes many fluid-filled sacs (cysts) a develop in the kidneys. The most common type of PKD is an inherited condition called autosomal dominant polycystic kidney disease (ADPKD). Polycystic kidney disease is a genetic condition. You get one faulty gene from each... Non-hereditary polycystic kidney disease In about.

Distrofia muscular

Patient information leaflet

Distrofia muscular

Muscular dystrophy is an inherited (genetic) disorder causing muscle weakness. Muscular dystrophy (MD) is the name given to a group of disorders which cause progressive muscle weakness (meaning it gets worse over time). Also, if a child has delayed motor mi... MD may be diagnosed using one or more of the following tests: A blood test for creatine.

Distonía

Patient information leaflet

Distonía

A dystonia is a lasting or frequently recurring and unwanted (involuntary) muscle contraction. It can affect one or more muscles in the body. Secondary dystonia Secondary means the dystonia has been caused by another condition or by something which has happened ... It is not caused by your genetic make-up. Some neurological conditions can cause.

Enfermedad de Huntington

Patient information leaflet

Enfermedad de Huntington

Between 5-10 in 100 people with Huntington's disease develop symptoms before they are 20. This is known as juvenile Huntington's disease. It can cause more severe symptoms. What causes Huntington's disease. Enfermedad de Huntington es caused by a defective gene that you inherit from your parents. Enfermedad de Huntington is an autosomal dominant.

Albinismo

Patient information leaflet

Albinismo

Albinismo is a rare enfermedad cardíaca (genetic) condition which reduces the amount of of melanin pigment in the skin, hair and/or eyes. People with albinism are often pale, with light-coloured irises. However, there are many types of albinism and people can... How common is albinism. Approximately 1 in 17,000 people in Europe and the USA have one de the.

Cáncer de mama en hombres

Patient information leaflet

Cáncer de mama en hombres

We think of breast cancer as a disease of women because it is usually women who are affected. However, breast cancer can develop occasionally in men too. Whatever your gender, it is very important to see a doctor as soon a... What is breast cancer. Cancer is a condition where cells multiply abnormally, affecting and distorting nearby body.

Lecturas adicionales y referencias

Historial del artículo

La información en esta página está escrita y revisada por pares por clínicos calificados.
  • 18 Aug 2020 | Última versión
  • 1 Sept 2011 | Publicado originalmente

Únete a la conversación

Comparte tus pensamientos o experiencias con otros en nuestro comunidades de pacientes.

Aviso legal: The views expressed in the community do not represent medical advice. For any health concerns, consult your GP or healthcare provider.
verificador de elegibilidad para la gripe

Pregunta, comparte, conecta.

Navega por discusiones, haz preguntas y comparte experiencias en cientos de temas de salud.

Suscríbete al boletín de Patient

Tu dosis semanal de consejos de salud claros y confiables, escritos para ayudarte a sentirte informado, seguro y en control.

Por favor, introduce una dirección de correo electrónico válida

Al suscribirte aceptas nuestros Política de Privacidad. Puedes darte de baja en cualquier momento. Nunca vendemos tus datos.