Entity Details

Primary name SAMD9L
Entity type gene
Source Source Link

Details

PrimaryID219285
RefseqGeneNG_053186
SymbolSAMD9L
Namesterile alpha motif domain containing 9 like
Chromosome7
Location7q21.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-05-05
ModificationDate2021-06-19

Ontological Relatives

UniProt IDsSAM9L_HUMAN

GO terms

Show/Hide Table
GOName
GO:0005737 cytoplasm
GO:0005769 early endosome

Diseases

Show/Hide Table
Disease IDSourceNameDescription
159550 OMIMAtaxia-pancytopenia syndrome (ATXPC)An autosomal dominant disorder characterized by cerebellar ataxia, variable hematologic cytopenias, and predisposition to bone marrow failure and myeloid leukemia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

8 interactions