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Details
Link-It Detail - Jax Mouse Phenotype - holoprosencephaly
Debug Stats
  • ### Total Build Time: 574 ms 21.507 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 362 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 264 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 571 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.572 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=550 ms Completed: 550 ms rowSize= 16.898 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
holoprosencephaly MP:0005157
Definition (1)
presence of a single forebrain hemisphere or lobe; often accompanied by a deficit in median facial development
Parents (1)
img abnormal brain development MP:0000913
Children (1)
img aprosencephaly MP:0006291
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal brain development MP:0000913
Genes (36)

Species:
human : 36
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanTTBK2146057tau tubulin kinase 2
Click here to display 77 evidence detail records.
HumanFOXP4116113forkhead box P4
Click here to display 77 evidence detail records.
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 77 evidence detail records.
HumanTCTN179600tectonic family member 1
Click here to display 77 evidence detail records.
HumanCC2D2A57545coiled-coil and C2 domain containing 2A
Click here to display 77 evidence detail records.
HumanTWSG157045twisted gastrulation homolog 1 (Drosophila)
Click here to display 77 evidence detail records.
HumanHHAT55733hedgehog acyltransferase
Click here to display 77 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
Click here to display 77 evidence detail records.
HumanCDON50937cell adhesion associated, oncogene regulated
Click here to display 77 evidence detail records.
HumanB9D127077B9 protein domain 1
Click here to display 77 evidence detail records.
HumanIFT17226160intraflagellar transport 172 homolog (Chlamydomonas)
Click here to display 77 evidence detail records.
HumanVAX111023ventral anterior homeobox 1
Click here to display 77 evidence detail records.
HumanSPRY210253sprouty homolog 2 (Drosophila)
Click here to display 77 evidence detail records.
HumanNOG9241noggin
Click here to display 77 evidence detail records.
HumanFOXH18928forkhead box H1
Click here to display 77 evidence detail records.
HumanCHRD8646chordin
Click here to display 77 evidence detail records.
HumanZIC27546Zic family member 2
Click here to display 77 evidence detail records.
HumanTGIF17050TGFB-induced factor homeobox 1
Click here to display 77 evidence detail records.
HumanTDGF16997teratocarcinoma-derived growth factor 1
Click here to display 77 evidence detail records.
HumanSIX36496SIX homeobox 3
Click here to display 77 evidence detail records.
HumanSTIL6491SCL/TAL1 interrupting locus
Click here to display 77 evidence detail records.
HumanSHH6469sonic hedgehog
Click here to display 77 evidence detail records.
HumanPTCH15727patched 1
Click here to display 77 evidence detail records.
HumanOTX25015orthodenticle homeobox 2
Click here to display 77 evidence detail records.
HumanNODAL4838nodal growth differentiation factor
Click here to display 77 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005157holoprosencephaly0self