BCL7B Products

Description

BCL7B is a member of the BCL7 family. Involved in cellular and developmental functions, BCL7B is located in the Williams-Beuren syndrome (WBS) critical region. Frequently expressed in heart, skeletal muscle and fetal liver, BLC7B can cause certain cardiovascular and musculo-skeletal defects.

Bioinformatics

Entrez	9275 Human
Uniprot	NP_001698 Human NP_001698.2 Human NM_001707 Human
Product By Gene ID	9275
Alternate Names	Allergen Hom s 3 B-cell CLL/lymphoma 7 protein family member B B-cell CLL/lymphoma 7B

Diseases related to BCL7B

Discover more about diseases related to BCL7B.

Williams Syndrome
Burkitt Lymphoma
Malignant Neoplasms
Neoplasms
Adenoma
Lymphoma
Coronary Heart Disease
Stenosis
Tumor Progression
Dermatitis, Atopic
Swine Diseases
Ileal Neoplasms
Sarcoma
Malignant Neoplasm Of Lung
Carcinoma
Carcinogenesis
Myopathy
Cardiovascular Diseases
Carcinoma, Large Cell
Lupus Erythematosus, Systemic

Pathways for BCL7B

View related products by pathway and learn more about each of the pathways below.

Transport
Cell Cycle
Immune Response
Lung Development
Dna Repair
Cognition
Pathogenesis
Nuclear Transport

Bioinformatics Tool for BCL7B

Discover related pathways, diseases and genes to BCL7B. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.