Skip to main content

caspase recruitment domain family member 14

The CARD14 gene provides instructions for making a protein that turns on (activates) a group of interacting proteins known as nuclear factor-kappa-B (NF-κB). The NF-κB protein complex regulates the activity of multiple genes, including genes that control the body's immune responses and inflammatory reactions. Inflammation is a normal immune system response to injury and foreign invaders (such as bacteria). The NF-κB protein complex also protects cells from certain signals that would otherwise cause them to self-destruct (undergo apoptosis).

Normal function

The CARD14 gene provides instructions for making a protein that turns on (activates) a group of interacting proteins known as nuclear factor-kappa-B (NF-κB). The NF-κB protein complex regulates the activity of multiple genes, including genes that control the body's immune responses and inflammatory reactions. Inflammation is a normal immune system response to injury and foreign invaders (such as bacteria). The NF-κB protein complex also protects cells from certain signals that would otherwise cause them to self-destruct (undergo apoptosis).

The CARD14 protein is found in many of the body's tissues, but it is particularly abundant in the skin. NF-κB signaling appears to play important roles in regulating inflammatory reactions in the skin and in promoting the survival of skin cells.

Conditions referring to this gene or chromosome

Other names

bcl10-interacting maguk protein 2

BIMP2

CAR14_HUMAN

CARD-containing MAGUK protein 2

card-maguk protein 2

carma 2

CARMA2

caspase recruitment domain family, member 14

caspase recruitment domain-containing protein 14

Related patient information and medicines

BRCA genes

Patient information leaflet

BRCA genes

There are a few known gene changes (mutations) that can increase the risk of certain cancers, and tests available for some of them, including BRCA1 and BRCA2 gene mutations. The BRCA1 and BRCA2 genes normally protect against certain cancers, particularly breast cancer and ovarian cancer. If there is a mutation in one of these genes then this may.

Pancreatic cancer

Patient information leaflet

Pancreatic cancer

In the UK, there is no screening programme for pancreatic cancer that is available fo... However screening is available for people who are at higher-than-average risk of pancreatic cancer. The European Registry of Hereditary Pancreatitis and Familial Pancreatic Cancer (EUROPAC) is an organisation based in Liverpool that is involved in researching.

Breast cancer facts and risk factors

Patient information leaflet

Breast cancer facts and risk factors

Most cases of breast cancer occur by chance. However, breast cancer does occur more often than usual in some families because of their genetic makeup. Most cases of breast cancer occur by chance. However, breast cancer does occur more often than usual in some families because of their genetic makeup. Genetic means that the condition is passed on.

Alcohol use disorder

Patient information leaflet

Alcohol use disorder

Many people drink alcohol. For some, alcohol is something that they enjoy in moderation. Other people drink alcohol at levels that are likely to lead to physical or mental health problems. Some people can find it very difficult to control, or stop, their drinking. What is alcohol use disorder. Alcohol use disorder means drinking alcohol in a way.

Alpha-1 antitrypsin deficiency

Patient information leaflet

Alpha-1 antitrypsin deficiency

If the balance tips and there is too much activity, lung tissue can start to become damaged by the enzymes. A1AT helps to balance the protease enzymes in the lungs and stop lung damage. What is alpha-1 antitrypsin deficiency. A1AT deficiency is an inherited genetic condition. A genetic condition is one that can be passed on from parents through.

Duchenne muscular dystrophy

Patient information leaflet

Duchenne muscular dystrophy

This is because of there being two X chromosomes in women: one X chromosome has the 'faulty' DMD gene; the other X chromosome has a normal gene, which compensates for the faulty one. In contrast, boys with the DMD gene do not have a second X chromosome and so they cannot compensate for the faulty gene. Therefore, boys with the DMD gene always have.

Further reading and references

Article history

The information on this page is written and peer reviewed by qualified clinicians.
  • 18 Aug 2020 | Latest version
  • 1 May 2017 | Originally published

Join the conversation

Share your thoughts or experiences with others in our patient communities.

Disclaimer: The views expressed in the community do not represent medical advice. For any health concerns, consult your GP or healthcare provider.
flu eligibility checker

Ask, share, connect.

Browse discussions, ask questions, and share experiences across hundreds of health topics.

Sign up to the Patient newsletter

Your weekly dose of clear, trustworthy health advice - written to help you feel informed, confident and in control.

Please enter a valid email address

By subscribing you accept our Privacy Policy. You can unsubscribe at any time. We never sell your data.