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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:abnormal neutrophil morphology
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Accession:MP:0005065 term browser browse the term
Definition:any structural anomaly of the immature or mature forms of a granular leukocyte that in its mature form has a nucleus with three to five lobes connected by slender threads of chromatin, and cytoplasm containing fine inconspicuous granules and stainable by neutral dyes
Synonyms:exact_synonym: abnormal neutrocyte morphology;   abnormal neutrophil leucocyte morphology;   abnormal neutrophil leukocyte morphology;   abnormal neutrophilic leucocyte morphology;   abnormal neutrophilic leukocyte morphology;   abnormal polymorphonuclear cell;   neutrophil structural abnormalities
 broad_synonym: abnormal PMN morphology;   abnormal polymorphonuclear leucocyte morphology;   abnormal polymorphonuclear leukocyte morphology;   abnormal polymorphonuclear neutrophil morphology;   abnormal polynuclear neutrophilic leucocyte morphology;   abnormal polynuclear neutrophilic leukocyte morphology



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increased neutrophil cell number term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ccdc39 coiled-coil domain 39 molecular ruler complex subunit IMP RGD PMID:31771992 RGD:150521527 NCBI chr 2:116,665,651...116,703,354
Ensembl chr 2:116,665,261...116,703,350
JBrowse link
G Ccdc39em1Jgn coiled-coil domain containing 39; CRISPR/Cas9 induced mutant 1, Jgn IMP RGD PMID:31771992 RGD:150521527
G Cftr CF transmembrane conductance regulator IMP RGD PMID:24608905 RGD:11566051 NCBI chr 4:46,561,269...46,728,759
Ensembl chr 4:46,560,885...46,728,756
JBrowse link
G Cftrem1Sage cystic fibrosis transmembrane conductance regulator; ZFN induced mutant 1 Sage IMP RGD PMID:24608905 RGD:11566051
G P2ry2 purinergic receptor P2Y2 IMP RGD PMID:19155635 RGD:2316657 NCBI chr 1:155,352,050...155,367,423
Ensembl chr 1:155,351,165...155,367,632
JBrowse link
G Sh2b3 SH2B adaptor protein 3 IMP RGD PMID:25628389 RGD:12904914 NCBI chr12:34,731,934...34,753,617
Ensembl chr12:34,731,911...34,753,616
JBrowse link
G Sh2b3em2Mcwi SH2B adaptor protein 3; zinc finger nuclease induced mutant 2, Medical College of Wisconsin IMP RGD PMID:25628389 RGD:12904914

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5418
    hematopoietic system phenotype 250
      abnormal hematopoietic system morphology/development 230
        abnormal hematopoietic cell morphology 186
          abnormal blood cell morphology 99
            abnormal granulocyte morphology 43
              abnormal neutrophil morphology 11
                abnormal neutrophil cell number + 11
                abnormal neutrophil differentiation 0
Path 2
Term Annotations click to browse term
  mammalian phenotype 5418
    immune system phenotype 502
      abnormal immune system morphology 194
        abnormal immune system cell morphology 154
          abnormal leukocyte morphology 154
            abnormal myeloid leukocyte morphology 70
              abnormal granulocyte morphology 43
                abnormal neutrophil morphology 11
                  abnormal neutrophil cell number + 11
                  abnormal neutrophil differentiation 0
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