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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
Results Image: 4B
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant 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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last database update
07/29/2020
MGI 6.15
The Jackson Laboratory