Nipa1 | non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)

GeneMGI:2442058Synonyms: Spg6, A830014A18Rik, +1 more

Physiological systems

20 / 24 physiological systems tested

1 Significantly impacted by the knock-out

 Vision/eye

19 No significant impact

4 Not tested

Gene metrics:1Significant phenotypes
3Associated diseases
Expression examined in:45Adult tissues
0Embryo tissues

Phenotypes

abnormal lens morphology1 supporting datasetNipa1tm1a(KOMP)WtsihomozygoteEarly adult5.1x10-5 
* Does not have a P-value assigned because it was manually marked as significant.
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* This parameter was manually assessed for significance.
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lacZ Expression

Associated images

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Histopathology

IMPC related publications

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Nipa1tm1(EGFP_CreERT2)WtsiReporter-tagged deletion allele (with selection cassette)ES Cell
Nipa1tm1.1(EGFP_CreERT2)WtsiReporter-tagged deletion allele (post Cre, with no selection cassette)ES Cell
Nipa1tm1a(KOMP)WtsiKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Nipa1tm1e(KOMP)WtsiTargeted, non-conditional alleleES Cell
Nipa1tm2a(KOMP)WtsiKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell

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