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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cephalic neural fold morphology
Debug Stats
  • ### Total Build Time: 65 ms 24.702 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 408 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 282 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 197 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=7 ms Completed: 7 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 584 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.576 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=38 ms Completed: 38 ms rowSize= 19.795 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.178 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal cephalic neural fold morphology MP:0011259
Definition (1)
any structural anomaly of the elevated margins of the neural groove that are located in the future cephalic region of the embryo
Synonyms (1)
"abnormal cranial neural fold morphology" EXACT
Parents (1)
img abnormal neural fold morphology MP:0011256
Children (1)
img incomplete cephalic closure MP:0000928
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053806img abnormal neural fold morphology MP:0011256
Genes (42)

Species:
human : 42
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanUNC5B219699unc-5 homolog B (C. elegans)
INFERRED
HumanGRHL279977grainyhead-like 2 (Drosophila)
INFERRED
HumanRGMA56963RGM domain family, member A
INFERRED
HumanIFT5755081intraflagellar transport 57 homolog (Chlamydomonas)
INFERRED
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanGATAD2A54815GATA zinc finger domain containing 2A
INFERRED
HumanTRIM3351592tripartite motif containing 33
INFERRED
HumanTXN225828thioredoxin 2
INFERRED
HumanPLXNB223654plexin B2
INFERRED
HumanPATZ123598POZ (BTB) and AT hook containing zinc finger 1
INFERRED
HumanPIP5K1C23396phosphatidylinositol-4-phosphate 5-kinase, type I, gamma
INFERRED
HumanCELSR19620cadherin, EGF LAG seven-pass G-type receptor 1
INFERRED
HumanGCM29247glial cells missing homolog 2 (Drosophila)
INFERRED
HumanNOG9241noggin
img Jax MP, Pubmed Id: 8536979, MOUSE PHENOTYPE ID: MGI:1096327
img Jax MP, Pubmed Id: 8536979, MOUSE PHENOTYPE ID: MGI:1096327
img Jax MP, Pubmed Id: 10688202, MOUSE PHENOTYPE ID: MGI:104327
img Jax MP, Pubmed Id: 9811592, MOUSE PHENOTYPE ID: MGI:97451
HumanIKBKAP8518inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
INFERRED
HumanAXIN18312axin 1
img Jax MP, Pubmed Id: 10688202, MOUSE PHENOTYPE ID: MGI:104327
img Jax MP, Pubmed Id: 8536979, MOUSE PHENOTYPE ID: MGI:1096327
img Jax MP, Pubmed Id: 9811592, MOUSE PHENOTYPE ID: MGI:97451
img Jax MP, Pubmed Id: 8536979, MOUSE PHENOTYPE ID: MGI:1096327
HumanFZD37976frizzled family receptor 3
INFERRED
HumanVCL7414vinculin
INFERRED
HumanTULP37289tubby like protein 3
INFERRED
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
INFERRED
HumanRPL386169ribosomal protein L38
INFERRED
HumanPTCH15727patched 1
INFERRED
HumanMAPK85599mitogen-activated protein kinase 8
INFERRED
HumanPOR5447P450 (cytochrome) oxidoreductase
INFERRED
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011259abnormal cephalic neural fold morphology0self