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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 hemoglobin content
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Accession:MP:0005563 term browser browse the term
Definition:deviation from the normal total hemoglobin content in the circulating blood
Synonyms:exact_synonym: abnormal haemoglobin content



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decreased hemoglobin content term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
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 Lrrk2 leucine-rich repeat kinase 2 IMP RGD PMID:23799078 RGD:13462048 NCBI chr 7:122,826,696...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:23799078 RGD:13462048
increased glycosylated hemoglobin level term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mc4r melanocortin 4 receptor IMP RGD PMID:24400148 RGD:13825242 NCBI chr18:60,419,832...60,421,719
Ensembl chr18:60,419,832...60,421,719
JBrowse link
G Mc4rm1Hubr melanocortin 4 receptor; ENU induced mutation 1, Hubr IMP RGD PMID:24400148 RGD:13825242

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5417
    hematopoietic system phenotype 250
      abnormal hematopoietic system morphology/development 230
        abnormal hematopoietic cell morphology 186
          abnormal blood cell morphology 99
            abnormal erythrocyte morphology 45
              abnormal hemoglobin 20
                abnormal hemoglobin content 14
                  abnormal cellular hemoglobin content + 0
                  abnormal glycosylated hemoglobin level + 7
                  abnormal hemoglobin concentration distribution width + 0
                  decreased hemoglobin content 7
                  increased hemoglobin content 0
Path 2
Term Annotations click to browse term
  mammalian phenotype 5417
    hematopoietic system phenotype 250
      abnormal hematopoietic system morphology/development 230
        abnormal hematopoietic cell morphology 186
          abnormal myeloid cell morphology 108
            abnormal erythroid lineage cell morphology 45
              abnormal erythrocyte morphology 45
                abnormal hemoglobin 20
                  abnormal hemoglobin content 14
                    abnormal cellular hemoglobin content + 0
                    abnormal glycosylated hemoglobin level + 7
                    abnormal hemoglobin concentration distribution width + 0
                    decreased hemoglobin content 7
                    increased hemoglobin content 0
paths to the root