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Details
Link-It Detail - Jax Mouse Phenotype - photoreceptor inner segment degeneration
Debug Stats
  • ### Total Build Time: 19 ms 20.931 KB
  • CONCEPT_NAME gt=4 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= 394 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 602 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 4.308 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 13.922 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.178 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
photoreceptor inner segment degeneration MP:0008580
Definition (1)
retrogressive pathologic change in the photoreceptor region which contains the machinery of the cell (mitochondria, golgi, endoplasmic reticulum, etc) and where opsin molecules are assembled and passed to be part of the outer segment region
Parents (1)
img abnormal photoreceptor inner segment morphology MP:0003730
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal photoreceptor inner segment morphology MP:0003730
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal photoreceptor inner segment morphology MP:0003730
img mammalian phenotype MP:0000001img vision/eye phenotype MP:000539112img abnormal photoreceptor inner segment morphology MP:0003730
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanASIC39311acid-sensing (proton-gated) ion channel 3
img Jax MP, Pubmed Id: 11182090, MOUSE PHENOTYPE ID: MGI:103555
img Jax MP, Pubmed Id: 22002997, MOUSE PHENOTYPE ID: MGI:1343101
img Jax MP, Pubmed Id: 18032602, MOUSE PHENOTYPE ID: MGI:1277215
img Jax MP, Pubmed Id: 19117938, MOUSE PHENOTYPE ID: MGI:2159339
HumanKAT2A2648K(lysine) acetyltransferase 2A
img Jax MP, Pubmed Id: 18032602, MOUSE PHENOTYPE ID: MGI:1277215
img Jax MP, Pubmed Id: 11182090, MOUSE PHENOTYPE ID: MGI:103555
img Jax MP, Pubmed Id: 19117938, MOUSE PHENOTYPE ID: MGI:2159339
img Jax MP, Pubmed Id: 22002997, MOUSE PHENOTYPE ID: MGI:1343101
HumanCLCN31182chloride channel, voltage-sensitive 3
img Jax MP, Pubmed Id: 18032602, MOUSE PHENOTYPE ID: MGI:1277215
img Jax MP, Pubmed Id: 11182090, MOUSE PHENOTYPE ID: MGI:103555
img Jax MP, Pubmed Id: 19117938, MOUSE PHENOTYPE ID: MGI:2159339
img Jax MP, Pubmed Id: 22002997, MOUSE PHENOTYPE ID: MGI:1343101
HumanBBS1582Bardet-Biedl syndrome 1
img Jax MP, Pubmed Id: 18032602, MOUSE PHENOTYPE ID: MGI:1277215
img Jax MP, Pubmed Id: 22002997, MOUSE PHENOTYPE ID: MGI:1343101
img Jax MP, Pubmed Id: 11182090, MOUSE PHENOTYPE ID: MGI:103555
img Jax MP, Pubmed Id: 19117938, MOUSE PHENOTYPE ID: MGI:2159339
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008580photoreceptor inner segment degeneration0self