C19orf40 |
FANCM |
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Gene Name | chromosome 19 open reading frame 40 | Fanconi anemia, complementation group M | |
Image | |||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 4 interactors: APP EME2 FANCM TERT | 8 interactors: APITD1 APP C19orf40 ECT2 EME2 STRA13 SUMO1 TRIM27 | |
Entrez ID | 91442 | 57697 | |
HPRD ID | 14547 | 13876 | |
Ensembl ID | ENSG00000187790 | ||
Uniprot IDs | K7EKQ4 Q9BTP7 | B2RTQ9 Q8IYD8 | |
PDB IDs | 2LYH 2M9M 2M9N 4BXO 4M6W | 4BXO 4DAY 4DRB 4E45 | |
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | anemia
arise
atm
deficiency
encoding
failure
fanconi
fertility
germ
hypogonadism
includes
instability
maintenance
males
meiotic
neonates
overlaid
partially
pgcs
phenotypes
primordial
progressive
propagate
propagation
repair
sexes
testicular
true
|
||
Tagcloud (Difference) ? | anemia
arise
atm
deficiency
encoding
failure
fanconi
fertility
germ
hypogonadism
includes
instability
maintenance
males
meiotic
neonates
overlaid
partially
pgcs
phenotypes
primordial
progressive
propagate
propagation
repair
sexes
testicular
true
|
||
Tagcloud (Intersection) ? |