Description: | catenin alpha 1 [Source:VGNC Symbol;Acc:VGNC:3958] |
Synonyms: | |
Other ID(s): | ENSPTRG00000017291 |
Protein Accession Numbers: | XP_009448023, XP_009448022, XP_016809389, XP_009448018 |
Statistics: | ClinVar(3636) gnomAD(575) COSMIC(772) PTM(98) |
∙ 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.
ENST00000302763 You are here now!
ENST00000355078
ENST00000517533
ENST00000517656
ENST00000517980
ENST00000518381
ENST00000518825
ENST00000518910
ENST00000519113
ENST00000519116
ENST00000519309
ENST00000519634
ENST00000519768
ENST00000520158
ENST00000520260
ENST00000520339
ENST00000520520
ENST00000520522
ENST00000520865
ENST00000521368
ENST00000521640
ENST00000521683
ENST00000521724
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 | ||||||
PF01044 | Vinculin | Vinculin family | 333-867 | CL0705 | VBS-like | Homo sapiens |
PF01044 | Vinculin | Vinculin family | 19-339 | CL0705 | VBS-like | Homo sapiens |
Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
---|---|---|---|---|---|
Hereditary Nonpolyposis Colorectal Neoplasms | Neoplasms ; Digestive System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Nutritional and Metabolic Diseases ; | 0.636 | 0.483 | ||
Leukemia, Myelocytic, Acute | Neoplasms ; | 0.636 | 0.483 | ||
Acute Myeloid Leukemia, M1 | Neoplasms ; | 0.636 | 0.483 | ||
Gastrointestinal Stromal Tumors | Neoplasms ; Digestive System Diseases ; | 0.636 | 0.483 | ||
Hereditary non-polyposis colorectal cancer syndrome | N/A | 0.636 | 0.483 | ||
Hereditary Nonpolyposis Colorectal Cancer | Neoplasms ; Digestive System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Nutritional and Metabolic Diseases ; | 0.636 | 0.483 | ||
Hereditary Diffuse Gastric Cancer | Neoplasms ; Digestive System Diseases ; | 0.636 | 0.483 | ||
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 | Eye Diseases ; | 0.636 | 0.483 | ||
Patterned dystrophy of retinal pigment epithelium | Eye Diseases ; | 0.636 | 0.483 | ||
Acute Myeloid Leukemia (AML-M2) | Neoplasms ; | 0.636 | 0.483 | ||
Hematopoetic Myelodysplasia | Hemic and Lymphatic Diseases ; | 0.636 | 0.483 | ||
Gastrointestinal Stromal Sarcoma | Neoplasms ; Digestive System Diseases ; | 0.636 | 0.483 | ||
MYELODYSPLASTIC SYNDROME | Hemic and Lymphatic Diseases ; | 0.636 | 0.483 | ||
Butterfly-shaped pigmentary macular dystrophy | N/A | 0.636 | 0.483 | ||
NO RESULT FOUND |