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Human Disease and Mouse Model Detail
Human Disease Neutropenia, Severe Congenital, 3, Autosomal Recessive; SCN3
OMIM ID: 610738
Synonyms Agranulocytosis, Infantile; Kostmann Disease; Neutropenia, Severe Congenital
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     HAX1* Hax1   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.04
The Jackson Laboratory