B4DV47 (B4DV47_HUMAN) Unreviewed, UniProtKB/TrEMBL
Last modified
April 3, 2013.
Version 26.
History...
Names and origin
| Protein names | Submitted name: cDNA FLJ57893, highly similar to Parafibromin EMBL BAG62559.1 |
| Organism | Homo sapiens (Human) EMBL BAG62559.1 |
| Taxonomic identifier | 9606 [NCBI] |
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 316 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
Sequences
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References
| [1] | "NEDO human cDNA sequencing project focused on splicing variants." Wakamatsu A., Yamamoto J., Kimura K., Ishii S., Watanabe K., Sugiyama A., Murakawa K., Kaida T., Tsuchiya K., Fukuzumi Y., Kumagai A., Oishi Y., Yamamoto S., Ono Y., Komori Y., Yamazaki M., Kisu Y., Nishikawa T. Isogai T.Submitted (OCT-2007) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE. Tissue: Small intestine EMBL BAG62559.1. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK300929 mRNA. Translation: BAG62559.1. |
| IPI | IPI00909174. |
| UniGene | Hs.378996. |
3D structure databases | |
| ProteinModelPortal | B4DV47. |
| ModBase | Search... |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Phylogenomic databases | |
| HOGENOM | HOG000199494. |
| HOVERGEN | HBG091448. |
| OrthoDB | EOG4PC9RV. |
Family and domain databases | |
| InterPro | IPR007852. RNA_pol_access_fac_Cdc73. [Graphical view] |
| PANTHER | PTHR12466. PTHR12466. 1 hit. |
| Pfam | PF05179. CDC73. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 35475354. |
Entry information
| Entry name | B4DV47_HUMAN | ||||||||
| Accession | Primary (citable) accession number: B4DV47 | ||||||||
| Entry history |
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| Entry status | Unreviewed (UniProtKB/TrEMBL) | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||

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