A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Gene Dmel\hop

General Information
SymbolDmel\hopSpeciesD. melanogaster
NamehopscotchAnnotation symbolCG1594
Feature typeprotein_coding_geneFlyBase IDFBgn0004864
Created / Updated2003-12-01/2003-12-01
Genomic Location
Chromosome (arm)XRecombination map1-34.6
Cytogenetic map10B5-10B6Sequence locationX:11,254,932..11,262,130 [-]
Map ( GBrowse ) detailed view
hide Summary Information
Automatically generated summary

See sections below for more information
The gene hopscotch is referred to in FlyBase by the symbol hop (CG1594, FBgn0004864). It has the cytological map location 10B5-10B6. Its sequence location is X:11254932..11262130. Its molecular function is described as: Janus kinase activity; protein-tyrosine kinase activity; non-membrane spanning protein tyrosine kinase activity; ATP binding; metallopeptidase activity; protein binding; zinc ion binding. It is involved in the biological processes described with 40 unique terms, many of which group under: anatomical structure development; immune response; sensory organ development; organ morphogenesis; cell division; gamete generation; ovarian follicle cell development; defense response; biopolymer modification; reproductive developmental process; embryonic pattern specification. 69 alleles are reported. The phenotypes of these alleles are annotated with 62 unique terms, many of which group under: organ system; peripheral nervous system; embryonic/larval hemocoel; nervous system; abdominal ventral denticle belt; adult segment; embryonic/larval tracheal system; follicle cell; thoracic segment; adult mesothoracic segment; portion of tissue. It has one annotated transcript and one annotated polypeptide.

External Summaries
hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
hop: hopscotch
The wild-type allele of hop is required for the continued cell division of all diploid cells as well as the establishment of the normal array of segments. Most of the mutants are homozygous late zygotic (L-P) lethals; one mutant is a larval lethal; two other mutants have some adult survivors (hemizygous males being morphologaically normal, but 40% of the homzygous females and 85% of the hemizygous females showing major defects). Most of the heteroallelic females are lethal, with the following exceptions:
            
 
            genotype      percent viable 
            ____________________________ 
             
            hop29/hop25   12% 
            hop3/hop25    16% 
            hop14/hop25   40% 
            hop12/hop25   68% 
            hop27/hop25   100% 
            hop32/hop25   100% 
            hop33/hop25   100% 
             
             
             
All viable heteroallelic combinations are female sterile, failing to produce eggs or laying abnormal eggs that are small, with a clear chorion and with chorionic filaments absent or partially fused (Perrimon and Mahowald, 1986a). There is a maternal effect on thoracic and abdominal segments, the most extreme embryos [produced from homozygous l(1)hop germline clones that have not received a paternal copy of hop+] showing defects in the posterior spiracles and in segments T2 (denticle belt deleted). T3, A4, and A5 (segment missing) and A8 (segment reduced in size); the least extreme mutant embryos from germline clones show defects in segment A5. Defects visible in early segmentation stages. The extent of the defects is dependent on the strength of the maternal alleles and the paternal contribution. Wild-type sperm can rescue all defects, except those in A5. A few of the rescued progeny hatch and develop into adults.
Tum: Tumorous
Dominant tumorous gene that is a temperature-sensitive lethal at 29 in hemizygous males and homozygous females; about two-thirds of the hemizygous males survive at 18 and one-quarter of these have melanotic tumors. Males raised at 26 and heterozygous females raised at 29 survive to adulthood, but show melanotic masses in the abdominal cavity or small black specks in the legs, wings, or thorax. Mutant larvae kept at 29 show enlargement of the lymph glands in the late second- or early third-instar larvae, but no melanotic masses. By mid third-instar, the lymph glands are large and diffuse and the gastric caeca have become encapsulated and melanized. By late third-instar, the larvae have melanotic masses in the body cavity, lack lymph glands, and have reduced, encapsulated and melanized gastric caeca as well as encapsulated and melanized muscles and fat bodies. These mutants do not survive beyond the late third-instar or the early pupal stage. When lymph glands from Tum larvae are injected into adult female hosts, transplantable neoplasms are produced. Melanization, at first associated with the leg joints and later with the head, thorax, and abdomen, takes place; also abdominal bloating. The lymph glands become melanotic and the abdomen is filled with encapsulated masses before the premature death of the injected individuals. Injection of Tum tissue other than lymph glands fails to produce these effects. The melanotic neoplasms can be transplanted into a succession of hosts in which they produce the same abnormalities. The neoplastic cells resemble hemocytes; some cell lines are melanotic and others are unpigmented, but in both types, the tissue, when transplanted, grows rapidly in the hosts and kills them.
hide Detailed Mapping Data
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
10B5-10B6  
Limits computationally determined from genome sequence between P{EP}CG11756EP1610 and P{EP}CG32666EP1452  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
10B6-10B6
(determined by in situ hybridisation)  
10B6-10B6
(determined by in situ hybridisation)  
Experimentally Determined Recombination Data
Location
1-34.6
 
Left of (cM)
Right of (cM)
Notes
Molecular Map Data
Gene Order (in direction of increasing cytology)
References
In direction of increasing cytology: dsh+ anon-10Ba- hop-
Gene Order (overall orientation not stated)
References
hide Gene Model & Products
Please see the GBrowse view of Dmel\hop for information on other features
detailed view FBtr0073456 FBtr0073457 FBtr0073482 FBtr0112813 FBtr0073490 FBtr0073491 FBtr0073488 FBtr0073483 FBtr0073492 FBpp0073312 FBpp0073313 FBpp0073338 FBti0071723 FBti0024932 FBti0052587 FBti0068320
Comments on Gene Model
DGC clone HL03036 appears problematic: incomplete CDS
hide Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Associated CDS (aa)
FBtr0073457
  5085
  1177
Additional Transcript Data & Comments
Reported size (kB)
5.4, 5.1 (northern blot)
Comments
External Data
Crossreferences
hide Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kD)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
hop-PA  
FBpp0073313  
135.1  
1177  
7.25  
Additional Polypeptide Data & Comments
Reported size (kD)
Comments
External Data
Linkouts
PANTHER - Protein classification by function, families, and pathways
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
    deletion
    comment=Approximate endpoints of a 5bp deletion reported to be at residue 201 within the JH6 domain.
    evidence=experimental
    deletion
    comment=Approximate endpoints of a 4bp deletion reported to be at residue 1121 at the C-terminal end of the kinase domain.
    evidence=experimental
    point mutation
    comment=One of two amino acid substitutions observed in mutant. Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=G11261467A
    pr_change=R10K|hop-PA
    reported_pr_change=R10K
    point mutation
    comment=hop[J1A.1] was generated in a hop[Tum] background. Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. The mutation is within the JH7 domain.
    evidence=experimental
    na_change=C11261237T
    pr_change=L87F|hop-PA
    reported_pr_change=L87F
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=G11260973M
    pr_change=G175R|hop-PA
    reported_pr_change=G175R
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=C11260760A
    pr_change=Q246K|hop-PA
    reported_pr_change=Q246K
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=A11260553T
    pr_change=K315@|hop-PA
    reported_pr_change=K315@
    point mutation
    evidence=experimental
    na_change=G11260474A
    pr_change=G341E|hop-PA
    reported_na_change=G1641A
    reported_pr_change=G341E
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=G11258124A
    pr_change=E695K|hop-PA
    reported_pr_change=E695K
    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. The A592G substitution, also observed in the mutant strain, appears to be a polymorphism, since a G residue is present at this site in the reference sequence.
    evidence=experimental
    pr_change=W741@|hop-PA
    reported_pr_change=W741@
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=C11257775A
    pr_change=S773@|hop-PA
    reported_pr_change=S773@
    point mutation
    comment=One of two amino acid substitutions observed in mutant. Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=C11257349R
    pr_change=Y892@|hop-PA
    reported_pr_change=Y892@
    point mutation
    comment=hop[F1.1] was generated in a hop[Tum] background. Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. The mutation is within the C terminal kinase domain.
    evidence=experimental
    na_change=G11257207A
    pr_change=E940K|hop-PA
    reported_pr_change=E940K
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=T11256488C
    pr_change=I1011T|hop-PA
    reported_pr_change=I1011T
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=C11256263T
    pr_change=S1062F|hop-PA
    reported_pr_change=S1062F
    point mutation
    comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
    evidence=experimental
    na_change=C11255991T
    pr_change=Q1131@|hop-PA
    reported_pr_change=Q1131@
    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=W1134@|hop-PA
    reported_pr_change=W1134@
    hide External Data
    Linkouts
    DEDB - Drosophila exon database: splicing graphs
    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
     embryonic stage | early
     embryonic stage-adult stage
    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
        FLIGHT - Cell culture data for RNAi and other high-throughput technologies
        FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
        GEO (NCBI) - Gene expression data: microarray and other high-throughput technologies
        hide Alleles & Phenotypes
        hide Summary of Allele Phenotypes
        Lethality
        Allele
        Other Phenotypes
        Allele
        Sterility
        Allele
        Phenotype manifest in
        Allele