Cep78 RT-PCR Gene Expression Assay

Gene Expression Data
Assay Details

Assay

Reference:	J:252169 Nikopoulos K, et al., Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects. Am J Hum Genet. 2016 Sep 1;99(3):770-776
Assay type:	RT-PCR
MGI Accession ID:	MGI:6110558
Gene symbol:	Cep78
Gene name:	centrosomal protein 78

Probe:

Cep78-pA, Cep78-pB

Results

Image: 4B

	Sample Information		Bands	Other Sample Information
Lane	Age	Structure	Size Not Specified	Amount	Genetic Background	Mutant Allele(s)	Sex
E13	E13.0 (a)	TS21: eye	Strong (b)	Not Specified	Not Specified		Not Specified
P0	P0	TS27: eye	Present (c)	Not Specified	Not Specified		Not Specified
P7	P7	TS28: eye	Present (c)	Not Specified	Not Specified		Not Specified
P21	P21	TS28: eye	Present (d)	Not Specified	Not Specified		Not Specified
P65	P65	TS28: eye	Present (d)	Not Specified	Not Specified		Not Specified
P90	P90	TS28: eye	Present (d)	Not Specified	Not Specified		Not Specified
P120	P120	TS28: eye	Present (d)	Not Specified	Not Specified		Not Specified

Notes:
(a) Age of embryo at noon of plug day not specified in reference.
(b) Authors report high expression at embryonic stages.
(c) Authors report a progressive decrease at perinatal stages.
(d) Authors report expression reaches a plateau at adulthood.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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