Entity Details
Primary name |
BMS1_HUMAN |
Entity type |
UniProt |
Source |
Source Link |
Details
Accession | Q14692 |
EntryName | BMS1_HUMAN |
FullName | Ribosome biogenesis protein BMS1 homolog |
TaxID | 9606 |
Evidence | evidence at protein level |
Length | 1282 |
SequenceStatus | complete |
DateCreated | 2002-12-13 |
DateModified | 2021-06-02 |
Subcellular Location
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Subcellular Location |
Nucleus |
Domains
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Domain | Name | Category | Type |
IPR007034 | Ribosome biogenesis protein BMS1/TSR1, C-terminal | Domain | Domain |
IPR012948 | AARP2CN | Domain | Domain |
IPR027417 | P-loop containing nucleoside triphosphate hydrolase | Family | Homologous superfamily |
IPR030387 | Bms1/Tsr1-type G domain | Domain | Domain |
IPR037875 | Ribosome biogenesis protein Bms1, N-terminal | Domain | Domain |
IPR039761 | Ribosome biogenesis protein Bms1/Tsr1 | Family | Family |
Diseases
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Disease ID | Source | Name | Description |
107600 | OMIM | Aplasia cutis congenita, non-syndromic (ACC) | A disorder characterized by congenital absence of a portion of skin in a localized or widespread area of the body. The lesions are most commonly localized on the scalp, however aplasia cutis congenita can affect any part of the body. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
5 interactions