A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Gene Dmel\mmy

General Information
SymbolDmel\mmySpeciesD. melanogaster
NamemummyAnnotation symbolCG9535
Feature typeprotein_coding_geneFlyBase IDFBgn0259749
Created / Updated2008-06-26/2008-06-26
Genomic Location
Chromosome (arm)2LRecombination map2-16
Cytogenetic map26D7-26D7Sequence location2L:6,468,538..6,473,919 [-]
Map ( GBrowse ) detailed view
hide Summary Information
Automatically generated summary

See sections below for more information
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hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
mmy: mummy
Embryonic lethal; mouth parts and denticles poorly differentiated.
hide Detailed Mapping Data
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
26D7-26D7  
Limits computationally determined from genome sequence between P{lacW}l(2)k09923k09923&P{lacW}CG9523k07502b and P{EP}Sec61αEP2180  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
26D7-26E1
Experimentally Determined Recombination Data
Location
Left of (cM)
Right of (cM)
Notes
Molecular Map Data
Gene Order (in direction of increasing cytology)
References
Gene Order (overall orientation not stated)
References
hide Gene Model & Products
Please see the GBrowse view of Dmel\mmy for information on other features
detailed view FBtr0079270 FBtr0079269 FBtr0079268 FBtr0079267 FBpp0078900 FBpp0078899 FBpp0078898 FBpp0078897 FBti0024695 FBti0027588 FBti0044893 FBti0077964 FBti0055131 FBti0036396 FBti0026379 FBti0021807 FBti0010773 FBti0025937 FBti0041579
Comments on Gene Model
hide Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Associated CDS (aa)
FBtr0079268
  2098
  520
FBtr0079269
  1919
  483
Additional Transcript Data & Comments
Reported size (kB)
Comments
External Data
Crossreferences
hide Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kD)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
mmy-PA  
FBpp0078898  
58.2  
520  
7.22  
mmy-PB  
FBpp0078899  
54.2  
483  
6.47  
Additional Polypeptide Data & Comments
Reported size (kD)
Comments
External Data
Linkouts
Crossreferences
InterPro domains - A database of protein families, domains, and functional sites
hide Sequences Consistent with the Gene Model
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
    Maps to
    Does NOT map to
    Identified with
    hide Mapped Features & Mutations
    Please see GBrowse or insertion reports for information on insertions of transgenic constructs and features not listed here
    Type
    Symbol & Location
    Additional Notes
    References
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=T6471405A
    pr_change=L124|mmy-PA,L87|mmy-PB
    reported_pr_change=L124@
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=G6471334A
    pr_change=G148R|mmy-PA,G111R|mmy-PB
    reported_pr_change=G148R
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=G6471328A
    pr_change=G150S|mmy-PA,G113S|mmy-PB
    reported_pr_change=G150S
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=C6469956T
    pr_change=T151I|mmy-PA,T114I|mmy-PB
    reported_pr_change=T151I
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=T6469866C
    pr_change=L181P|mmy-PA,L144P|mmy-PB
    reported_pr_change=181P
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=T6469818A
    pr_change=I197N|mmy-PA,I160N|mmy-PB
    reported_pr_change=I197N
    point mutation
    comment=G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation. (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    pr_change=W199|mmy-PA,W162|mmy-PB
    reported_pr_change=W199@
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=C6469797T
    pr_change=S204L|mmy-PA,S167L|mmy-PB
    reported_pr_change=S204L
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=G6469680A
    pr_change=G243E|mmy-PA,G206E|mmy-PB
    reported_pr_change=G243E
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=G6469626T
    pr_change=G261V|mmy-PA,G224V|mmy-PB
    reported_pr_change=G261V
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=C6469600T
    pr_change=Q270|mmy-PA,Q233|mmy-PB
    reported_pr_change=Q270@
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=T6469152A
    pr_change=V419D|mmy-PA,V382D|mmy-PB
    reported_pr_change=V419D
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=T6469107A
    pr_change=V434E|mmy-PA,V397E|mmy-PB
    reported_pr_change=V434E
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=T6469080G
    pr_change=L443R|mmy-PA,L406R|mmy-PB
    reported_pr_change=L443R
    hide External Data
    Linkouts
    Crossreferences
    hide Expression Data
    FlyBase-Curated Data
    Transcript and
    Protein data
    Please see the FlyBase Gene Expression Report for details of gene expression from the literature.
    hide Summary of Transcript Expression
    Stage
    Tissue/Position
    Reference
    Marker for
      Subcellular Localization
      CV Term
      hide Summary of Polypeptide Expression
      Stage
      Tissue/Position
      Reference
      Marker for
        Subcellular Localization
        CV Term
        hide External Data & Images
        Linkouts
        hide Alleles & Phenotypes
        hide Summary of Allele Phenotypes
        Lethality
        Allele
        Other Phenotypes
        Allele
        Sterility
        Allele
        Phenotype manifest in
        Allele
        larval hindgut & embryo
        commissure & embryo
        connective & embryo
        ventral nerve cord commissure & stage 16 embryo
        longitudinal connective & stage 16 embryo
        chordotonal organ & stage 16 embryo
        hide Classical Alleles ( 38 )
        For All Classical Alleles Show

        Allele of mmyClassMutagenStocksKnown lesion
        mmy038510 Yes
        mmy11 --
        mmy20 --
        mmyDG196121 --
        mmyEP20161 --
        mmyG131hypomorph
          0 --
          mmyGA740 Yes
          mmyGA7600 --
          mmyH0530 Yes
          mmyH120amorph
            0 --
            mmyIK630 Yes
            mmyIL070 Yes
            mmyJ1201amorph
              0 --
              mmyKG043491 --
              mmyKG086171 --
              mmyLM16loss of function0 Yes
              mmyLM1loss of function0 Yes
              mmyLM210 Yes
              mmyLM23loss of function0 --
              mmyLM24loss of function0 Yes
              mmyLM29loss of function0 --
              mmyLM320 Yes
              mmyLM33loss of function0 --
              mmyLM35loss of function0 Yes
              mmyLM42loss of function0 Yes
              mmyLM44loss of function0 --
              mmyLM45loss of function0 --
              mmyLM47loss of function0 Yes
              mmyLM49loss of function0 --
              mmyLM51loss of function0 Yes
              mmyLM55loss of function0 Yes
              mmyLM59loss of function0 --
              mmyQ180amorph
                0 --
                mmyZ234
                  0 --
                  mmyZ237
                    0 --
                    mmyk13717b
                      0 --
                      mmyunspecified
                        0 --
                        mmyΔ2016-30 Yes
                        hide Alleles Carried on Transgenic Constructs ( 1 )
                        For All Alleles Carried on Transgenic Constructs Show

                        Allele of mmyClassMutagenStocksKnown lesion
                        mmyGD142420 Yes
                        hide Aneuploid Aberrations
                        Useful deficiency
                        Useful duplication
                        Disrupted in
                        Not disrupted in
                        hide Transgenic Constructs & Insertions
                        Transgenic Constructs
                        Type of construct
                        Name
                        Expression data
                        UAS construct
                        Insertions
                        Type of insertions
                        Name
                        Expression data
                        insertion of enhancer trap
                        insertion of mobile activating element
                        hide Related Comments
                        Please look at the allele reports for the complete phenotype data
                        Two EMS induced alleles were identified in a screen for mutations affecting commissure formation in the CNS of the embryo.
                        Mutation in mmy alters tracheal tube size in embryos without affecting other aspects of tracheal development including primary branch budding and outgrowth or branch fusion.
                        hide Gene Ontology: Function, Process & Cellular Component ( 11 )
                        hide Molecular Function
                        CV term
                        References
                        inferred from mutant phenotype
                        inferred from sequence or structural similarity
                        inferred from sequence or structural similarity
                        inferred from sequence or structural similarity with SGD_LOCUS:QRI1; SGD:S0002261
                        hide Biological Process
                        CV term
                        References
                        inferred from mutant phenotype
                        inferred from mutant phenotype
                        inferred from mutant phenotype
                        inferred from mutant phenotype
                        inferred from mutant phenotype
                        inferred from mutant phenotype
                        inferred from mutant phenotype
                        inferred from mutant phenotype
                        inferred from mutant phenotype
                        inferred from mutant phenotype