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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vision
Debug Stats
  • ### Total Build Time: 132 ms 24.097 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 358 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 191 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 172 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=0 Completed: 0 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 3.654 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.565 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=109 ms Completed: 109 ms rowSize= 16.311 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal vision MP:0002090
Definition (1)
inability or decreased ability to see
Synonyms (1)
"visual defects" EXACT
Parents (1)
img abnormal eye physiology MP:0005253
Children (8)
img double vision MP:0006150
img myopia MP:0003100
img abnormal visual contrast sensitivity MP:0011831
img tunnel vision MP:0006152
img abnormal visual acuity MP:0011832
img hypermetropia MP:0006153
img blindness MP:0002001
img hemeralopia MP:0008145
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053914img abnormal eye physiology MP:0005253
Genes (52)

Species:
human : 52
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanCPLX3594855complexin 3
Click here to display 41 evidence detail records.
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanNXNL1115861nucleoredoxin-like 1
Click here to display 41 evidence detail records.
HumanGJA1084694gap junction protein, alpha 10, 62kDa
Click here to display 41 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
Click here to display 41 evidence detail records.
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
INFERRED
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Click here to display 41 evidence detail records.
HumanNYX60506nyctalopin
Click here to display 41 evidence detail records.
HumanDNASE2B58511deoxyribonuclease II beta
Click here to display 41 evidence detail records.
HumanSLC17A757030solute carrier family 17 (vesicular glutamate transporter), member 7
INFERRED
HumanERC226059ELKS/RAB6-interacting/CAST family member 2
Click here to display 41 evidence detail records.
HumanMERTK10461c-mer proto-oncogene tyrosine kinase
INFERRED
HumanSLC4A79497solute carrier family 4, sodium bicarbonate cotransporter, member 7
INFERRED
HumanAP3B18546adaptor-related protein complex 3, beta 1 subunit
Click here to display 41 evidence detail records.
HumanBFSP28419beaded filament structural protein 2, phakinin
Click here to display 41 evidence detail records.
HumanTYRO37301TYRO3 protein tyrosine kinase
INFERRED
HumanTYR7299tyrosinase
Click here to display 41 evidence detail records.
HumanNR2E17101nuclear receptor subfamily 2, group E, member 1
INFERRED
HumanELOVL46785ELOVL fatty acid elongase 4
Click here to display 41 evidence detail records.
HumanSLC6A66533solute carrier family 6 (neurotransmitter transporter), member 6
Click here to display 41 evidence detail records.
HumanSLC4A36508solute carrier family 4 (anion exchanger), member 3
INFERRED
HumanRHO6010rhodopsin
Click here to display 41 evidence detail records.
HumanRELA5970v-rel avian reticuloendotheliosis viral oncogene homolog A
INFERRED
HumanOPN1LW5956opsin 1 (cone pigments), long-wave-sensitive
Click here to display 41 evidence detail records.
HumanRBP45950retinol binding protein 4, plasma
Click here to display 41 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002090abnormal vision0self