Slc35c2 | solute carrier family 35, member C2

GeneMGI:2385166Synonyms: D2Wsu58e, Ovcov1, +1 more

Physiological systems

17 / 24 physiological systems tested

2 Significantly impacted by the knock-out

 Integument Behavior/neurological

15 No significant impact

7 Not tested

Gene metrics:3Significant phenotypes
0Associated diseases
Expression examined in:48Adult tissues
42Embryo tissues

Phenotypes

decreased thigmotaxis4 supporting datasetsSlc35c2tm1.1(KOMP)VlcghomozygoteEarly adult3.35x10-5 
abnormal behavior1 supporting datasetSlc35c2tm1.1(KOMP)VlcghomozygoteEarly adult6.08x10-5 
abnormal coat/ hair morphology1 supporting datasetSlc35c2tm1.1(KOMP)VlcghomozygoteEarly adult1.57x10-5 
* 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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Slc35c2tm1(KOMP)VlcgReporter-tagged deletion allele (with selection cassette)ES Cell
mouse
Slc35c2tm1.1(KOMP)VlcgReporter-tagged deletion allele (post Cre, with no selection cassette)mouse
Slc35c2tm1a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
Slc35c2tm33609(L1L2_gt1)KO first allele (reporter-tagged insertion with conditional potential)targeting vector

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