BG:DS09218.1 , Dbf4, BG:DS09218.2
Dbf4 homolog - regulatory subunit of Cdc7-Dbf4 dimer - associated with the origin recognition complex activates the kinase function of its dimerization partner, thus triggering the initiation of cellular DNA replication
Please see the JBrowse view of Dmel\chif for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Multiphase exon postulated: this gene shares a region of coding sequence with an overlapping gene, but different reading frames are utilized in the overlapping coding region; overlap >20aa.
Gene model reviewed during 5.43
Gene model reviewed during 5.50
Complex/atypical overlap: Shares 5' UTR with downstream gene; in addition, one transcript isoform shares 3' UTR with downstream gene.
Gene model reviewed during 6.27
6.6, 6.5 (northern blot)
1711, 1695 (aa)
May be proteolytically cleaved to produce a N-terminal 50 kDa product.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\chif using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
Comment: anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
JBrowse - Visual display of RNA-Seq signals
View Dmel\chif in JBrowse





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Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
polyclonal
Hypomorphic mutations in chif cause thin, fragile chorions and female sterility, and eliminate chorion gene amplification. Null alleles have the additional phenotypes of rough eyes and thin thoracic bristles; phenotypes often associated with disruption of the normal cell cycle.
chif is involved in processes in addition to chorion gene amplification.
Mutations at the chif locus cause defects in midoogenesis.
5 alleles are discussed but are not named.