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Details
Link-It Detail - Jax Mouse Phenotype - abnormal anterior eye segment morphology
Debug Stats
  • ### Total Build Time: 105 ms 22.778 KB
  • CONCEPT_NAME gt=5 ms Completed: 4 ms rowSize= 408 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 265 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 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=5 ms Completed: 5 ms rowSize= 3.316 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.565 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=88 ms Completed: 88 ms rowSize= 15.174 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 anterior eye segment morphology MP:0005193
Definition (1)
any structural anomaly of any of the parts of the eye that lie in front of, or ventral to, the lens (inclusive)
Synonyms (1)
"abnormal anterior segment" EXACT
Parents (1)
img abnormal eye morphology MP:0002092
Children (7)
img abnormal eye posterior chamber morphology MP:0005299
img abnormal conjunctiva morphology MP:0001310
img abnormal anterior uvea morphology MP:0005194
img abnormal lens morphology MP:0001303
img abnormal cornea morphology MP:0001312
img anterior staphyloma MP:0008815
img abnormal eye anterior chamber morphology MP:0005205
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053914img abnormal eye morphology MP:0002092
Genes (291)

Species:
human : 291
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanAREGB727738amphiregulin B
INFERRED
HumanPRSS56646960protease, serine, 56
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanVSX2338917visual system homeobox 2
INFERRED
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanTBC1D32221322TBC1 domain family, member 32
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanSIX5147912SIX homeobox 5
INFERRED
HumanTOM1L2146691target of myb1-like 2 (chicken)
INFERRED
HumanSLC25A25114789solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 25
INFERRED
HumanEGLN3112399egl-9 family hypoxia-inducible factor 3
INFERRED
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
INFERRED
HumanPYGO290780pygopus homolog 2 (Drosophila)
INFERRED
HumanSLX484464SLX4 structure-specific endonuclease subunit
INFERRED
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED
HumanZNRF384133zinc and ring finger 3
INFERRED
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanCOL18A180781collagen, type XVIII, alpha 1
INFERRED
HumanDOCK580005dedicator of cytokinesis 5
INFERRED
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED
HumanFKRP79147fukutin related protein
INFERRED
HumanVPS33A65082vacuolar protein sorting 33 homolog A (S. cerevisiae)
INFERRED
HumanNFKBIZ64332nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta
INFERRED
HumanSMOC164093SPARC related modular calcium binding 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005193abnormal anterior eye segment morphology0self