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Gene Expression Data
Assay Details
Assay
Reference: J:228552 Ercan-Sencicek AG, et al., Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. Eur J Hum Genet. 2015 Feb;23(2):165-72
Assay type: Western blot
MGI Accession ID: MGI:5812428
Gene symbol: Diaph1
Gene name: diaphanous related formin 1
Antibody: Anti-Diaph1 (ab11172)
Assay notes: Two antibodies were described, but the one used in this assay was not specified; either MGI:5812118 or MGI:5812121 could have been used.
Results Image: S5A
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Genetic BackgroundMutant Allele(s)Sex
Lane 1 P TS28: brain Present Not Specified Not Specified
Lane 2 P TS28: brain Absent involves: 129S1/Sv * C57BL/6 Diaph1tm1Asal/Diaph1tm1AsalNot Specified

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
04/23/2024
MGI 6.23
The Jackson Laboratory