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Details
Link-It Detail - Jax Mouse Phenotype - abnormal Ammon gyrus morphology
Debug Stats
  • ### Total Build Time: 91 ms 69.462 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 354 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 188 bytes
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  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 1.521 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 2.921 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 62.224 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal Ammon gyrus morphology MP:0000815
Definition (1)
any structural anomaly of one or both of the two interlocking gyri of the hippocampus formation; a circonvolution of rhinencephalon, the grey substance of which is rich in big pyramidal neuronal cells
Synonyms (1)
"abnormal Ammon horn morphology" EXACT
Parents (1)
img abnormal hippocampus morphology MP:0000807
Children (3)
img abnormal hippocampus CA2 region morphology MP:0008265
img abnormal hippocampus CA1 region morphology MP:0008263
img abnormal hippocampus CA3 region morphology MP:0008267
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal hippocampus morphology MP:0000807
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal hippocampus morphology MP:0000807
Genes (43)

Species:
human : 43
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanARX170302aristaless related homeobox
INFERRED
HumanLHX564211LIM homeobox 5
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 21452199, MOUSE PHENOTYPE ID: MGI:2444430
img Jax MP, Pubmed Id: 17218254, MOUSE PHENOTYPE ID: MGI:98869
img Jax MP, Pubmed Id: 9012509, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 16377659, MOUSE PHENOTYPE ID: MGI:88175
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 11493561, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 16338116, MOUSE PHENOTYPE ID: MGI:99400
img Jax MP, Pubmed Id: 18434600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 10325223, MOUSE PHENOTYPE ID: MGI:107792
img Jax MP, Pubmed Id: 14637104, MOUSE PHENOTYPE ID: MGI:97173
HumanNEUROD663974neuronal differentiation 6
INFERRED
HumanPLXNA355558plexin A3
img Jax MP, Pubmed Id: 16338116, MOUSE PHENOTYPE ID: MGI:99400
img Jax MP, Pubmed Id: 11493561, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 17218254, MOUSE PHENOTYPE ID: MGI:98869
img Jax MP, Pubmed Id: 14637104, MOUSE PHENOTYPE ID: MGI:97173
img Jax MP, Pubmed Id: 10325223, MOUSE PHENOTYPE ID: MGI:107792
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 9012509, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 21452199, MOUSE PHENOTYPE ID: MGI:2444430
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 16377659, MOUSE PHENOTYPE ID: MGI:88175
img Jax MP, Pubmed Id: 18434600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
HumanFEZF255079FEZ family zinc finger 2
INFERRED
HumanPOMT229954protein-O-mannosyltransferase 2
img Jax MP, Pubmed Id: 9012509, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 17218254, MOUSE PHENOTYPE ID: MGI:98869
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 10325223, MOUSE PHENOTYPE ID: MGI:107792
img Jax MP, Pubmed Id: 16377659, MOUSE PHENOTYPE ID: MGI:88175
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 14637104, MOUSE PHENOTYPE ID: MGI:97173
img Jax MP, Pubmed Id: 16338116, MOUSE PHENOTYPE ID: MGI:99400
img Jax MP, Pubmed Id: 18434600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 11493561, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 21452199, MOUSE PHENOTYPE ID: MGI:2444430
HumanTRIB228951tribbles homolog 2 (Drosophila)
INFERRED
HumanSS18L126039synovial sarcoma translocation gene on chromosome 18-like 1
INFERRED
HumanDPYSL410570dihydropyrimidinase-like 4
INFERRED
HumanTUBA1A7846tubulin, alpha 1a
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 16338116, MOUSE PHENOTYPE ID: MGI:99400
img Jax MP, Pubmed Id: 18434600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 21452199, MOUSE PHENOTYPE ID: MGI:2444430
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 14637104, MOUSE PHENOTYPE ID: MGI:97173
img Jax MP, Pubmed Id: 9012509, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 17218254, MOUSE PHENOTYPE ID: MGI:98869
img Jax MP, Pubmed Id: 11493561, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 10325223, MOUSE PHENOTYPE ID: MGI:107792
img Jax MP, Pubmed Id: 16377659, MOUSE PHENOTYPE ID: MGI:88175
HumanTP737161tumor protein p73
INFERRED
HumanTNR7143tenascin R
INFERRED
HumanTLR37098toll-like receptor 3
INFERRED
HumanSNAP256616synaptosomal-associated protein, 25kDa
INFERRED
HumanSLC1A26506solute carrier family 1 (glial high affinity glutamate transporter), member 2
INFERRED
HumanRGS25997regulator of G-protein signaling 2, 24kDa
INFERRED
HumanPTPN65777protein tyrosine phosphatase, non-receptor type 6
INFERRED
HumanRELN5649reelin
INFERRED
HumanABCB15243ATP-binding cassette, sub-family B (MDR/TAP), member 1
INFERRED
HumanNPC14864Niemann-Pick disease, type C1
INFERRED
HumanNFIX4784nuclear factor I/X (CCAAT-binding transcription factor)
INFERRED
HumanNCAM14684neural cell adhesion molecule 1
INFERRED
HumanMT34504metallothionein 3
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 9012509, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 15917450, MOUSE PHENOTYPE ID: MGI:95388
img Jax MP, Pubmed Id: 17218254, MOUSE PHENOTYPE ID: MGI:98869
img Jax MP, Pubmed Id: 16338116, MOUSE PHENOTYPE ID: MGI:99400
img Jax MP, Pubmed Id: 18434600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 16377659, MOUSE PHENOTYPE ID: MGI:88175
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 21452199, MOUSE PHENOTYPE ID: MGI:2444430
img Jax MP, Pubmed Id: 11683995, MOUSE PHENOTYPE ID: MGI:107683
img Jax MP, Pubmed Id: 14637104, MOUSE PHENOTYPE ID: MGI:97173
img Jax MP, Pubmed Id: 10325223, MOUSE PHENOTYPE ID: MGI:107792
img Jax MP, Pubmed Id: 11493561, MOUSE PHENOTYPE ID: MGI:95388
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
INFERRED
HumanMAPT4137microtubule-associated protein tau
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000815abnormal Ammon gyrus morphology0self