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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 erythrocyte cell number
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Accession:MP:0001586 term browser browse the term
Definition:altered number of the cells that transport oxygen, red blood cells, per unit
Synonyms:exact_synonym: abnormal RBC count;   abnormal definitive erythrocyte cell number;   abnormal erythrocyte count;   abnormal red blood cell count;   erythrocyte count abnormalities
 alt_id: MP:0000214


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decreased erythrocyte cell number term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cd59em1Ask CD59 molecule; CRISPR/Cas9 induced mutant1, Ask IMP RGD PMID:28212662 RGD:13792592
G Cd59b CD59b molecule IMP RGD PMID:28212662 RGD:13792592 NCBI chr 3:90,459,085...90,477,571
Ensembl chr 3:90,459,162...90,478,847 		JBrowse link
G F8 coagulation factor VIII IAGP DNA,protein:missense mutation,decreased activity:exon:p.L176P(rat) RGD PMID:20626616 RGD:7245964 NCBI chr18:140,848...172,330
Ensembl chr18:140,955...171,857 		JBrowse link
G F8m1Ycb coagulation factor VIII, procoagulant component; mutation 1, Ycb IAGP DNA,protein:missense mutation,decreased activity:exon:p.L176P(rat) RGD PMID:20626616 RGD:7245964
G Kit KIT proto-oncogene receptor tyrosine kinase IMP RGD PMID:1912576 RGD:5133424 NCBI chr14:32,547,459...32,624,694
Ensembl chr14:32,548,877...32,624,652 		JBrowse link
G KitWs KIT proto-oncogene receptor tyrosine kinase; mutant 1 IMP RGD PMID:1912576 RGD:5133424
G Lrrk2 leucine-rich repeat kinase 2 IMP RGD PMID:24244710 PMID:23799078 RGD:12880447, RGD:13462048 NCBI chr 7:122,826,712...122,987,711
Ensembl chr 7:122,826,696...122,987,703 		JBrowse link
G Lrrk2em1Sage leucine-rich repeat kinase 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs IMP RGD PMID:24244710 RGD:12880447
Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5372
    hematopoietic system phenotype 243
      abnormal hematopoietic system morphology/development 223
        abnormal hematopoietic cell morphology 179
          abnormal blood cell morphology 96
            abnormal erythrocyte morphology 42
              abnormal erythrocyte cell number 12
                abnormal fetal derived definitive erythrocyte cell number + 0
                decreased erythrocyte cell number + 12
                increased erythrocyte cell number + 0
Path 2
Term Annotations click to browse term
  mammalian phenotype 5372
    hematopoietic system phenotype 243
      abnormal hematopoietic system morphology/development 223
        abnormal hematopoietic cell morphology 179
          abnormal myeloid cell morphology 102
            abnormal erythroid lineage cell morphology 42
              abnormal erythrocyte morphology 42
                abnormal erythrocyte cell number 12
                  abnormal fetal derived definitive erythrocyte cell number + 0
                  decreased erythrocyte cell number + 12
                  increased erythrocyte cell number + 0
paths to the root