Histone H2B Polyclonal Antibody, 50ul[BT-AP04028] Monoclonal Antibodies Mutations in this gene cause

Mutations in this gene cause Joubert syndrome

There are multiple components involved in the NER pathway| including Xeroderma pigmentosum (XP) A-G and V| Cockayne syndrome (CS) A and B| and trichothiodystrophy (TTD) group A| etc

TATA-box-binding protein that coordinates these activities is transcription factor IID (TFIID)

This gene product is a key molecule in ion channel regulation and synaptic exocytosis

This gene belongs to the R-spondin family

Histone H2B Polyclonal Antibody, 50ul[BT-AP04028] Monoclonal Antibodies Mutations in this gene causeH2BFS (H2B Histone Family Member S (Pseudogene)) is a Pseudogene. Diseases associated with H2BFS include endometrial stromal sarcoma. Among its related pathways are Packaging Of Telomere Ends. GO annotations related to this gene include sequence specific DNA binding and protein heterodimerization activity. An important paralog of this gene is HIST1H2BH.