fs(1)1182, fs(1)A1182
Please see the JBrowse view of Dmel\mh for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Gene model reviewed during 5.52
Gene model reviewed during 5.43
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\mh 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).
mh protein is deposited into the nuclei of oocytes during oogenesis. It is expressed in germline cells but not in somatic follicle cells in the oocyte. mh protein is detected in early stages of spermatogenesis but not in mature sperm. It is also present in both the maternal and paternal pronuclei before the first zygotic mitosis.
JBrowse - Visual display of RNA-Seq signals
View Dmel\mh in JBrowsePlease Note FlyBase no longer curates genomic clone accessions so this list may not be complete
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
mh mutants are strict maternal effect mutations that cause the production of haploid gynogenetic embryos (eggs are fertilised but only maternal chromosomes participate in development).
In an acentriolar cell line made from the maternal haploid (mh) female sterile mutant Cyclin B does not localise to 2 spots per metaphase, as it does in wild type Kc cells.
Source for merge of: mh CG9203