Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

CRRD ID: 1349319
Species: Homo sapiens
CRRD Object: Gene
Symbol: BCAP31
Name: B cell receptor associated protein 31
Acc ID: DOID:9006413
Term: Neonatal Severe Encephalopathy due to Mecp2 Mutations
Definition: null
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
QualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
 IAGPRGD:138186538554872ClinVarClinVar Annotator: match by term: Encephalopathy, neonatal severe, due to MECP2 mutations

PMID:15351775, PMID:15689435, PMID:16080119, PMID:17088400, PMID:17172942, PMID:22578097, PMID:23220634, PMID:26930212, PMID:28492532
Go Back to source page   Continue to Ontology report

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.