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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 interfrontal bone morphology
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Accession:MP:0008818 term browser browse the term
Definition:any structural anomaly or presence of a bone between the frontal bones in the skull; an extra bony plate within the anterior fontanelle that is not usually present
Synonyms:exact_synonym: interfrontal bone dysplasia



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abnormal interfrontal bone morphology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gli3 GLI-Kruppel family member GLI3 IAGP MGI PMID:5806166 PMID:6049666 NCBI chr13:15,638,308...15,904,611
Ensembl chr13:15,637,820...15,904,611
JBrowse link
G Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano IAGP MGI PMID:19047372 NCBI chr 6:113,044,389...113,054,205
Ensembl chr 6:113,043,843...113,054,294
JBrowse link
G H2az2 H2A.Z histone variant 2 IAGP MGI PMID:19047372 NCBI chr11:6,377,226...6,394,511
Ensembl chr11:6,377,229...6,394,443
JBrowse link
G Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) IAGP MGI PMID:26234751 NCBI chr11:68,876,527...68,899,286
Ensembl chr11:68,876,523...68,899,286
JBrowse link
G Tet1 tet methylcytosine dioxygenase 1 IAGP MGI PMID:22246904 NCBI chr10:62,640,349...62,723,242
Ensembl chr10:62,640,349...62,744,775
JBrowse link
G Wnt9a wingless-type MMTV integration site family, member 9A IAGP MGI PMID:16818445 NCBI chr11:59,197,675...59,224,378
Ensembl chr11:59,197,754...59,224,378
JBrowse link
G Zic3 zinc finger protein of the cerebellum 3 IAGP MGI PMID:1018005 NCBI chr  X:57,075,988...57,081,990
Ensembl chr  X:57,068,060...57,087,096
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 16242
    craniofacial phenotype 1575
      abnormal craniofacial morphology 1575
        abnormal craniofacial bone morphology 997
          abnormal cranium morphology 981
            abnormal viscerocranium morphology 724
              abnormal interfrontal bone morphology 7
Path 2
Term Annotations click to browse term
  mammalian phenotype 16242
    skeleton phenotype 3197
      abnormal skeleton morphology 3013
        abnormal axial skeleton morphology 1722
          abnormal craniofacial bone morphology 997
            abnormal cranium morphology 981
              abnormal neurocranium morphology 344
                abnormal interfrontal bone morphology 7
paths to the root