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Pathways

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 fetal derived definitive erythrocyte morphology
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Accession:MP:0011240 term browser browse the term
Definition:any structural anomaly of a fetal liver derived enucleated erythrocyte, which matures in macrophage islands within the liver, enucleates, and then enters the bloodstream; these resemble adult erythrocytes in that they are small (3- to 6- times smaller than primitive erythrocytes) and produce adult hemoglobins
Synonyms:exact_synonym: abnormal foetal derived definitive erythrocyte morphology
 related_synonym: abnormal liver derived definitive erythrocyte morphology
 xref: CL:0002357



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abnormal fetal derived definitive erythrocyte morphology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cpeb4 cytoplasmic polyadenylation element binding protein 4 IAGP MGI PMID:25220394 NCBI chr11:31,820,911...31,885,635
Ensembl chr11:31,822,211...31,885,634
JBrowse link
abnormal fetal derived definitive erythrocyte cell number term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mir451a microRNA 451a IAGP MGI PMID:20679397 NCBI chr11:77,963,996...77,964,067
Ensembl chr11:77,963,996...77,964,067
JBrowse link
G Spi1 spleen focus forming virus (SFFV) proviral integration oncogene IAGP MGI PMID:14739214 NCBI chr 2:90,912,750...90,946,104
Ensembl chr 2:90,912,735...90,946,101
JBrowse link
decreased fetal derived definitive erythrocyte cell number term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ccbe1 collagen and calcium binding EGF domains 1 IAGP MGI PMID:23426945 NCBI chr18:66,189,926...66,424,909
Ensembl chr18:66,178,373...66,435,812
JBrowse link
G Cpeb4 cytoplasmic polyadenylation element binding protein 4 IAGP MGI PMID:25220394 NCBI chr11:31,820,911...31,885,635
Ensembl chr11:31,822,211...31,885,634
JBrowse link
G Epor erythropoietin receptor IAGP MGI PMID:23795291 NCBI chr 9:21,870,193...21,874,915
Ensembl chr 9:21,870,193...21,874,802
JBrowse link
G Ikzf1 IKAROS family zinc finger 1 IAGP MGI PMID:12871645 NCBI chr11:11,634,970...11,722,930
Ensembl chr11:11,634,980...11,722,926
JBrowse link
G Jarid2 jumonji and AT-rich interaction domain containing 2 IAGP MGI PMID:9864150 NCBI chr13:44,881,817...45,075,119
Ensembl chr13:44,882,950...45,075,119
JBrowse link
G Kdm1a lysine (K)-specific demethylase 1A IAGP MGI PMID:23795291 NCBI chr 4:136,277,844...136,330,127
Ensembl chr 4:136,277,851...136,330,034
JBrowse link
G Mcm3 minichromosome maintenance complex component 3 IAGP MGI PMID:26456157 NCBI chr 1:20,873,188...20,890,536
Ensembl chr 1:20,873,192...20,890,536
JBrowse link
G Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform IAGP MGI PMID:21514445 NCBI chr11:51,989,651...52,013,576
Ensembl chr11:51,989,508...52,018,605
JBrowse link
increased fetal derived definitive erythrocyte cell number term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ttc7 tetratricopeptide repeat domain 7 IAGP MGI PMID:16093647 NCBI chr17:87,590,328...87,689,197
Ensembl chr17:87,590,314...87,689,197
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 16478
    hematopoietic system phenotype 5344
      abnormal hematopoietic system morphology/development 4885
        abnormal hematopoietic cell morphology 4062
          abnormal blood cell morphology 3051
            abnormal erythrocyte morphology 1632
              abnormal fetal derived definitive erythrocyte morphology 11
                abnormal fetal derived definitive erythrocyte cell number + 11
Path 2
Term Annotations click to browse term
  mammalian phenotype 16478
    hematopoietic system phenotype 5344
      abnormal hematopoietic system morphology/development 4885
        abnormal hematopoietic cell morphology 4062
          abnormal myeloid cell morphology 2938
            abnormal erythroid lineage cell morphology 1696
              abnormal erythrocyte morphology 1632
                abnormal fetal derived definitive erythrocyte morphology 11
                  abnormal fetal derived definitive erythrocyte cell number + 11
paths to the root