| Description: | core-binding factor subunit beta [Source:ZFIN;Acc:ZDB-GENE-980526-440] |
| Synonyms: | unp1266 |
| Other ID(s): | ZDB-GENE-980526-440, ENSDARG00000040917 |
| Protein Accession Numbers: | XP_005159106, NP_954679, XP_021323265, XP_009291807, XP_005159105, XP_021323264, XP_009291805, XP_005159104, XP_021323266, XP_021323263 |
| Statistics: | COSMIC(317) PTM(14) |
∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000290858 You are here now!
ENST00000412916
ENST00000561924
ENST00000563939
ENST00000564034
ENST00000565389
NP_001355636
NP_001355637
NP_001355638
NP_001355639
NP_001746 You are here now!
NP_074036
| Pfam Domain filter_list | Domain Name filter_list | Description filter_list | Positions filter_list | Clan filter_list | Clan Name filter_list | Organism filter_list |
|---|---|---|---|---|---|---|
| NO RESULT FOUND | ||||||
| PF02312 | CBF_beta | Core binding factor beta subunit | 1-168 | Homo sapiens | ||
| Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
|---|---|---|---|---|---|
| Bone Diseases, Developmental | Musculoskeletal Diseases ; | 0.627 | 0.414 | ||
| Malignant neoplasm of breast | Neoplasms ; Skin and Connective Tissue Diseases ; | 0.627 | 0.414 | ||
| Cleft Palate | Musculoskeletal Diseases ; Stomatognathic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.627 | 0.414 | ||
| Congenital Heart Defects | Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.627 | 0.414 | ||
| Leukemia, Myelocytic, Acute | Neoplasms ; | 0.627 | 0.414 | ||
| Acute myelomonocytic leukemia | Neoplasms ; | 0.627 | 0.414 | ||
| Acute Myeloid Leukemia, M1 | Neoplasms ; | 0.627 | 0.414 | ||
| Heterotopic Ossification | Pathological Conditions, Signs and Symptoms ; | 0.627 | 0.414 | ||
| Cleft palate, isolated | Musculoskeletal Diseases ; Stomatognathic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.627 | 0.414 | ||
| Acute Myeloid Leukemia (AML-M2) | Neoplasms ; | 0.627 | 0.414 | ||
| AML M4 Eo with inv(16) or t(16;16) | N/A | 0.627 | 0.414 | ||
| NO RESULT FOUND | |||||