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KRT6B

Reviewed August 2008

What is the official name of the KRT6B gene?

The official name of this gene is “keratin 6B.”

KRT6B is the gene's official symbol. The KRT6B gene is also known by other names, listed below.

What is the normal function of the KRT6B gene?

The KRT6B gene provides instructions for making a protein called keratin 6b or K6b. Keratins are a group of tough, fibrous proteins that form the structural framework of certain cells, particularly cells that make up the skin, hair, nails, and similar tissues. Keratin 6b is produced in the nails, the hair follicles, and the skin on the palms of the hands and soles of the feet. It is also found in the skin's sebaceous glands, which produce an oily substance called sebum.

Keratin 6b partners with a similar protein, keratin 17, to form molecules called keratin intermediate filaments. These filaments assemble into dense networks that provide strength and resiliency to the skin, nails, and other tissues. Networks of keratin filaments protect these tissues from being damaged by friction and other everyday physical stresses. Keratin 6b is also among several keratins involved in wound healing.

Does the KRT6B gene share characteristics with other genes?

The KRT6B gene belongs to a family of genes called KRT (keratins).

A gene family is a group of genes that share important characteristics. Classifying individual genes into families helps researchers describe how genes are related to each other. For more information, see What are gene families? in the Handbook.

How are changes in the KRT6B gene related to health conditions?

pachyonychia congenita - caused by mutations in the KRT6B gene

At least two mutations in the KRT6B gene have been identified in people with pachyonychia congenita type 2 (PC-2). One of these mutations changes a single protein building block (amino acid) in keratin 6b, while the other mutation deletes an amino acid from the protein.

The KRT6B mutations responsible for PC-2 change the structure of keratin 6b, preventing it from working effectively with keratin 17 and interfering with the assembly of the keratin intermediate filament network. Without this network, skin cells become fragile and are easily damaged, making the skin less resistant to friction and minor trauma. Even normal activities such as walking can cause skin cells to break down, resulting in the formation of painful blisters and calluses. In the sebaceous glands, abnormal keratin filaments lead to the development of cysts called steatocystomas. Defective keratin 6b also disrupts the growth and function of cells in the nails and hair follicles, which explains why the signs and symptoms of PC-2 also affect these tissues.

Where is the KRT6B gene located?

Cytogenetic Location: 12q12-q13

Molecular Location on chromosome 12: base pairs 51,126,701 to 51,132,176

The KRT6B gene is located on the long (q) arm of chromosome 12 between positions 12 and 13.

The KRT6B gene is located on the long (q) arm of chromosome 12 between positions 12 and 13.

More precisely, the KRT6B gene is located from base pair 51,126,701 to base pair 51,132,176 on chromosome 12.

See How do geneticists indicate the location of a gene? in the Handbook.

Where can I find additional information about KRT6B?

You and your healthcare professional may find the following resources about KRT6B helpful.

You may also be interested in these resources, which are designed for genetics professionals and researchers.

What other names do people use for the KRT6B gene or gene products?

  • CK 6B
  • CK6B
  • cytokeratin 6B
  • Cytokeratin-6B
  • K2C6B_HUMAN
  • K6B
  • K6b keratin
  • keratin, epidermal, type II, K6B
  • keratin, type II cytoskeletal 6B
  • KRTL1

Where can I find general information about genes?

The Handbook provides basic information about genetics in clear language.

These links provide additional genetics resources that may be useful.

What glossary definitions help with understanding KRT6B?

acids ; amino acid ; blister ; callus ; cell ; cysts ; cytokeratin ; domain ; gene ; hair follicle ; intermediate filaments ; keratin ; molecule ; motif ; mutation ; pachyonychia ; protein ; sign ; stress ; symptom ; tissue ; trauma

You may find definitions for these and many other terms in the Genetics Home Reference Glossary.

References (3 links)

 

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? in the Handbook.

 
Reviewed: August 2008
Published: January 23, 2009