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Details
Link-It Detail - Jax Mouse Phenotype - abnormal eye distance/ position
Debug Stats
  • ### Total Build Time: 476 ms 21.594 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 258 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 194 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.325 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.565 KB
  • CONCEPT_RELATIONSHIPS gt=445 ms Completed: 445 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 15.003 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal eye distance/ position MP:0001299
Definition (1)
abnormal placement of the eyes in relation to each other or in relation to other craniofacial structures
Synonyms (1)
"eye distance/ position abnormalities" EXACT
Parents (1)
img abnormal eye morphology MP:0002092
Children (5)
img hypertropia MP:0006199
img ocular hypertelorism MP:0001300
img ocular hypotelorism MP:0006197
img exophthalmos MP:0002750
img enophthalmos MP:0006198
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053914img abnormal eye morphology MP:0002092
Genes (44)

Species:
human : 44
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
Click here to display 18 evidence detail records.
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanTOM1L2146691target of myb1-like 2 (chicken)
Click here to display 18 evidence detail records.
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
INFERRED
HumanPGAP180055post-GPI attachment to proteins 1
INFERRED
HumanALX460529ALX homeobox 4
INFERRED
HumanIFT5755081intraflagellar transport 57 homolog (Chlamydomonas)
INFERRED
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanCDON50937cell adhesion associated, oncogene regulated
INFERRED
HumanHECTD125831HECT domain containing E3 ubiquitin protein ligase 1
Click here to display 18 evidence detail records.
HumanABCA523461ATP-binding cassette, sub-family A (ABC1), member 5
INFERRED
HumanKIF3A11127kinesin family member 3A
INFERRED
HumanITGB1BP19270integrin beta 1 binding protein 1
INFERRED
HumanHESX18820HESX homeobox 1
Click here to display 18 evidence detail records.
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
INFERRED
HumanTBX156913T-box 15
INFERRED
HumanSOS16654son of sevenless homolog 1 (Drosophila)
INFERRED
HumanSIX16495SIX homeobox 1
INFERRED
HumanRAF15894v-raf-1 murine leukemia viral oncogene homolog 1
INFERRED
HumanPTPN115781protein tyrosine phosphatase, non-receptor type 11
Click here to display 18 evidence detail records.
HumanPRKDC5591protein kinase, DNA-activated, catalytic polypeptide
INFERRED
HumanPITX35309paired-like homeodomain 3
Click here to display 18 evidence detail records.
HumanPITX25308paired-like homeodomain 2
Click here to display 18 evidence detail records.
HumanPDCD15133programmed cell death 1
INFERRED
HumanOTX25015orthodenticle homeobox 2
Click here to display 18 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001299abnormal eye distance/ position0self