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Gene Expression Data
Assay Details
Assay
Reference: J:178421 Dowdle WE, et al., Disruption of a ciliary B9 protein complex causes Meckel syndrome. Am J Hum Genet. 2011 Jul 15;89(1):94-110
Assay type: RT-PCR
MGI Accession ID: MGI:6370129
Gene symbol: B9d1
Gene name: B9 protein domain 1
Results Image: S2B Exon3/4-Exon7
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex
B9d1 +/+ E9.5 TS15: embryo Present Not Specified involves: C57BL/6 * FVB/N * SJL Not Specified
B9d1 +/- E9.5 TS15: embryo Weak Not Specified involves: C57BL/6 * FVB/N * SJL B9d1tm1d(EUCOMM)Wtsi/B9d1+Not Specified
B9d1 -/- E9.5 TS15: embryo Absent (a) Not Specified involves: C57BL/6 * FVB/N * SJL B9d1tm1d(EUCOMM)Wtsi/B9d1tm1d(EUCOMM)WtsiNot Specified
Notes:
(a) Authors state the wild-type transcript is almost completely abrogated in homozygous mutant embryos.
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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03/25/2025
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