Description: | tubulin, beta 2A class IIa [Source:RGD Symbol;Acc:1588452] |
Synonyms: | |
Other ID(s): | ENSRNOG00000017558 |
Protein Accession Numbers: | NP_001102589 |
Statistics: | ClinVar(45) PTM(63) |
∙ 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.
ENST00000333628
NP_001060
NP_001297244 You are here now!
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 | ||||||
PF00091 | Tubulin | Tubulin/FtsZ family, GTPase domain | 3-212 | CL0566 | Tubulin | Homo sapiens |
PF03953 | Tubulin_C | Tubulin C-terminal domain | 261-383 | CL0442 | Tubulin_C | Homo sapiens |
Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
---|---|---|---|---|---|
Cerebrovascular Disorders | Nervous System Diseases ; Cardiovascular Diseases ; | 0.707 | 0.31 | ||
Creutzfeldt-Jakob disease | Nervous System Diseases ; Mental Disorders ; | 0.707 | 0.31 | ||
Leukemia, Myelocytic, Acute | Neoplasms ; | 0.707 | 0.31 | ||
Acute Myeloid Leukemia, M1 | Neoplasms ; | 0.707 | 0.31 | ||
Juvenile-Onset Still Disease | Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ; | 0.707 | 0.31 | ||
New Variant Creutzfeldt-Jakob Disease | Nervous System Diseases ; Mental Disorders ; | 0.707 | 0.31 | ||
Creutzfeldt-Jakob Disease, Familial | Nervous System Diseases ; Mental Disorders ; | 0.707 | 0.31 | ||
Colorectal Cancer | Neoplasms ; Digestive System Diseases ; | 0.707 | 0.31 | ||
Acute Myeloid Leukemia (AML-M2) | Neoplasms ; | 0.707 | 0.31 | ||
Malformations of Cortical Development | Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.707 | 0.31 | ||
Juvenile arthritis | Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ; | 0.707 | 0.31 | ||
Intellectual Disability | Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; | 0.707 | 0.31 | ||
Juvenile psoriatic arthritis | Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ; | 0.707 | 0.31 | ||
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5 | N/A | 0.707 | 0.31 | ||
NO RESULT FOUND |