Homo sapiens Protein: RNF213 | |||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Summary | |||||||||||||||||||
InnateDB Protein | IDBP-485521.4 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | RNF213 | ||||||||||||||||||
Protein Name | ring finger protein 213 | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000425956 | ||||||||||||||||||
InnateDB Gene | IDBG-71708 (RNF213) | ||||||||||||||||||
Protein Structure |
![]() |
||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Probable E3 ubiquitin-protein ligase that may play a role in angiogenesis. May also have an ATPase activity. | ||||||||||||||||||
Subcellular Localization | Cytoplasm {ECO:0000269PubMed:21799892}. | ||||||||||||||||||
Disease Associations | Moyamoya disease 2 (MYMY2) [MIM:607151]: A progressive cerebral angiopathy characterized by bilateral intracranial carotid artery stenosis and telangiectatic vessels in the region of the basal ganglia. The abnormal vessels resemble a 'puff of smoke' (moyamoya) on cerebral angiogram. Affected individuals can develop transient ischemic attacks and/or cerebral infarction, and rupture of the collateral vessels can cause intracranial hemorrhage. Hemiplegia of sudden onset and epileptic seizures constitute the prevailing presentation in childhood, while subarachnoid bleeding occurs more frequently in adults. {ECO:0000269PubMed:21048783, ECO:0000269PubMed:21799892}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.Note=A chromosomal aberration involving ALO17 is associated with anaplastic large-cell lymphoma (ALCL). Translocation t(2;17)(p23;q25) with ALK. | ||||||||||||||||||
Tissue Specificity | Widely expressed (at protein level). {ECO:0000269PubMed:21799892}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
|
||||||||||||||||||
Gene Ontology | |||||||||||||||||||
Molecular Function |
|
||||||||||||||||||
Biological Process |
|
||||||||||||||||||
Cellular Component |
|
||||||||||||||||||
Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR001841
Zinc finger, RING-type IPR003593 AAA+ ATPase domain IPR027417 P-loop containing nucleoside triphosphate hydrolase |
||||||||||||||||||
PFAM |
PF13639
PF14634 |
||||||||||||||||||
PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00184
SM00382 |
||||||||||||||||||
TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q63HN8 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q63HN8 | ||||||||||||||||||
TrEMBL | H3BLU6 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 57674 | ||||||||||||||||||
UniGene | Hs.743310 | ||||||||||||||||||
RefSeq | XP_005257602 | ||||||||||||||||||
HUGO | HGNC:14539 | ||||||||||||||||||
OMIM | 613768 | ||||||||||||||||||
CCDS | |||||||||||||||||||
HPRD | 10716 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB046774 AB046838 AB537889 AC123764 AC124319 AF397204 AF397205 AK023871 AK025676 AK025914 AK026038 AK074030 AL832920 AL833201 BC032220 BC036891 BC040341 BX640932 BX647946 | ||||||||||||||||||
GenPept | AAH32220 AAH36891 AAH40341 AAN63520 AAN63521 BAB13380 BAB13444 BAB14708 BAB15212 BAB15280 BAB15330 BAB84856 BAK53191 CAE45967 CAH10615 CAH56189 CAH56308 | ||||||||||||||||||