OBO ID: DOID:0111080
Term Name: Fanconi anemia complementation group V Search Ontology:
Synonyms:
  • FANCV
Definition: A Fanconi anemia that has_material_basis_in homozygous mutation in the MAD2L2 gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/27500492
References:
Ontology: Human Disease   ( DOID:0111080 )
Relationships
is a type of:
disjoint_from:
OTHER Fanconi anemia complementation group V PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MAD2L2 ?Fanconi anemia, complementation group V 617243
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.