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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 cranial flexure morphology
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Accession:MP:0004203 term browser browse the term
Definition:any structural anomaly or absence of the sharp, ventrally concave bend in the developing midbrain of the embryo
Synonyms:exact_synonym: abnormal cephalic flexure morphology;   abnormal cerebral flexure morphology;   abnormal mesencephalic flexure morphology;   abnormal midbrain flexure morphology



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abnormal cranial flexure morphology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Apaf1 apoptotic peptidase activating factor 1 IAGP MGI PMID:9216040 NCBI chr10:90,825,173...90,918,688
Ensembl chr10:90,825,173...90,918,632
JBrowse link
G C2cd3 C2 calcium-dependent domain containing 3 IAGP MGI PMID:19004860 PMID:34211969 NCBI chr 7:100,021,440...100,119,366
Ensembl chr 7:100,021,440...100,119,359
JBrowse link
G Erbb3 erb-b2 receptor tyrosine kinase 3 IAGP MGI PMID:9362461 NCBI chr10:128,403,392...128,425,504
Ensembl chr10:128,403,392...128,425,521
JBrowse link
G Ift57 intraflagellar transport 57 IAGP MGI PMID:17027958 NCBI chr16:49,519,657...49,585,489
Ensembl chr16:49,519,596...49,585,489
JBrowse link
G Ift88 intraflagellar transport 88 IAGP MGI PMID:14603322 NCBI chr14:57,661,519...57,755,393
Ensembl chr14:57,661,519...57,755,393
JBrowse link
G Intu inturned planar cell polarity protein IAGP MGI PMID:20067783 NCBI chr 3:40,585,559...40,659,206
Ensembl chr 3:40,585,435...40,659,204
JBrowse link
G Rest RE1-silencing transcription factor IAGP MGI PMID:23022299 NCBI chr 5:77,413,273...77,434,279
Ensembl chr 5:77,413,338...77,434,279
JBrowse link
G Ttbk2 tau tubulin kinase 2 IAGP MGI PMID:30532139 NCBI chr 2:120,563,297...120,681,111
Ensembl chr 2:120,563,297...120,681,085
JBrowse link
G Wnt1 wingless-type MMTV integration site family, member 1 IAGP MGI PMID:2205396 NCBI chr15:98,687,738...98,691,711
Ensembl chr15:98,687,738...98,691,718
JBrowse link

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  mammalian phenotype 17097
    nervous system phenotype 4654
      abnormal nervous system morphology 3677
        abnormal nervous system development 1586
          abnormal brain development 831
            abnormal midbrain development 67
              abnormal cranial flexure morphology 9
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