تخطي إلى المحتوى الرئيسي

structural maintenance of chromosomes 3

ال SMC3 gene provides instructions for making a protein that is part of the structural maintenance of chromosomes (SMC) family. Within the nucleus, SMC proteins help regulate the structure and organisation of chromosomes.

Normal function

ال SMC3 gene provides instructions for making a protein that is part of the structural maintenance of chromosomes (SMC) family. Within the nucleus, SMC proteins help regulate the structure and organisation of chromosomes.

The protein produced from the SMC3 gene helps control chromosomes during cell division. Before cells divide, they must copy all of their chromosomes. The copied DNA from each chromosome is arranged into two identical structures, called sister chromatids, which are attached to one another during the early stages of cell division. The SMC3 protein is part of a protein group called the cohesin complex that holds the sister chromatids together.

Researchers believe that the SMC3 protein, as a structural component of the cohesin complex, also plays important roles in stabilizing cells' genetic information, repairing damaged DNA, and regulating the activity of certain genes that are essential for normal development.

Although the SMC3 protein is found primarily in the nucleus, some of this protein is transported out of cells. The exported protein, which is usually called bamacan, may be involved in sticking cells together (cell adhesion) and cell growth. Bamacan is a component of basement membranes, which are thin, sheet-like structures that separate and support cells in many tissues. Little else is known about the function of this protein outside the cell, but it appears to be important for normal development.

Conditions referring to this gene or chromosome

Other names

BAM

bamacan

basement membrane-associated chondroitin proteoglycan

BMH

chondroitin sulfate proteoglycan 6

chromosome-associated polypeptide

CSPG6

HCAP

SMC3_HUMAN

SMC3L1

Related patient information and medicines

الفحص الجيني

Patient information leaflet

الفحص الجيني

الفحص الجيني is a type من medical test that identifies changes in chromosomes, genes or proteins. Genetic tests examine a person's DNA in a variety of ways to assess a person's genetic health. We all have 46 chromosomes in our cells. Chromosomes are made from DNA (deoxyribonucleic acid). Genes are short sections of DNA and each chromosome.

الشيخوخة

Patient information leaflet

الشيخوخة

Ageing (also spelt aging) is the process of becoming older. This happens continually throughout life. It may also be that the presence or absence of certain genes allows people to live longer. With repeated dividing, the telomeres - protective structures at the end of the threads of genes (chromosomes) - become shorter, exposing the chromosomes to.

ابيضاض الدم الليمفاوي الحاد

Patient information leaflet

ابيضاض الدم الليمفاوي الحاد

Acute lymphoblastic leukaemia (ALL) is a condition where the bone marrow makes large numbers of abnormal immature lymphocytes. What is acute lymphoblastic leukaemia. Chromosomes are the parts in the cell which contain DNA - the genetic makeup of the cell. In some ... (These changes in chromosomes only occur in the leukaemia cells, not the normal.

الإجهاض والنزيف في بداية الحمل

Patient information leaflet

الإجهاض والنزيف في بداية الحمل

This may be referred to by doctors as a missed miscarriage. What causes miscarriage. It is thought that most early miscarriages are caused by a one-off problem with the chromosomes of the developing baby (fetus) in the womb. Chromosomes are the structures that contain the genetic information inherited from the parents. If a baby (fetus) doesn't.

متلازمة تيرنر

Patient information leaflet

متلازمة تيرنر

Turner syndrome is a genetic condition that only affects girls. The most characteristic features of the syndrome are being short, having certain physical features (detailed below), and ovaries that do not work properly. Can Turner syndrome be ... Turner syndrome is a genetic condition. This means that there is an abnormality with the genes of the.

ابيضاض الدم النقوي المزمن

Patient information leaflet

ابيضاض الدم النقوي المزمن

Chronic myeloid leukaemia (CML) is sometimes called chronic myelogenous leukaemia, chronic granulocytic leukaemia, أو chronic myelocytic leukaemia. What is chronic myeloid leukaemia. Chronic myeloid leukaemia (CML) is sometimes called chronic myelogenous leukaemia, chronic granulocytic leukaemia, or chronic myelocytic leukaemia. CML develops due.

قراءة إضافية ومراجع

تاريخ المقال

تمت كتابة المعلومات على هذه الصفحة ومراجعتها من قبل أطباء مؤهلين.
  • 13 Apr 2022 | أحدث إصدار
  • 1 أبريل 2022 | نُشر في الأصل

انضم إلى المحادثة

شارك أفكارك أو تجاربك مع الآخرين في مجتمعات المرضى.

تنويه: The views expressed in the community do not represent medical advice. For any health concerns, consult your GP or healthcare provider.
أداة التحقق من أهلية لقاح الإنفلونزا

اسأل، شارك، تواصل.

تصفح المناقشات، اطرح الأسئلة، وشارك التجارب عبر مئات المواضيع الصحية.

اشترك في النشرة الإخبارية للمرضى

جرعتك الأسبوعية من النصائح الصحية الواضحة والموثوقة - مكتوبة لمساعدتك على الشعور بالاطلاع والثقة والتحكم.

يرجى إدخال عنوان بريد إلكتروني صالح

من خلال الاشتراك، فإنك تقبل سياسة الخصوصية. يمكنك إلغاء الاشتراك في أي وقت. نحن لا نبيع بياناتك أبدًا.