Dystrophin-1

<p>This section provides any useful information about the protein, mostly biological knowledge.<p><a href='/help/function_section' target='_top'>More...</a></p>Functionⁱ

Sites

Regions

<p>The <a href="http://www.geneontology.org/">Gene Ontology (GO)</a> project provides a set of hierarchical controlled vocabulary split into 3 categories:<p><a href='/help/gene_ontology' target='_top'>More...</a></p>GO - Molecular functionⁱ

• actin binding Source: UniProtKB-KW
• zinc ion binding Source: InterPro

GO - Biological processⁱ

• acetylcholine transport Source: UniProtKB <p>Inferred from Mutant Phenotype</p> <p>Describes annotations that are concluded from looking at variations or changes in a gene product such as mutations or abnormal levels and includes techniques such as knockouts, overexpression, anti-sense experiments and use of specific protein inhibitors.</p> <p>More information in the <a href="http://geneontology.org/page/guide-go-evidence-codes#imp">GO evidence code guide</a></p> Inferred from mutant phenotypeⁱ
  • Ref.1

    "Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission."
    Bessou C., Giugia J.-B., Franks C.J., Holden-Dye L., Segalat L.
    Neurogenetics 2:61-72(1998) [PubMed] [Europe PMC] [Abstract]

    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM A), FUNCTION, TISSUE SPECIFICITY, DISRUPTION PHENOTYPE.
• forward locomotion Source: WormBaseInferred from mutant phenotypeⁱ
  • Ref.1

    "Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission."
    Bessou C., Giugia J.-B., Franks C.J., Holden-Dye L., Segalat L.
    Neurogenetics 2:61-72(1998) [PubMed] [Europe PMC] [Abstract]

    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM A), FUNCTION, TISSUE SPECIFICITY, DISRUPTION PHENOTYPE.
• locomotory behavior Source: WormBaseInferred from mutant phenotypeⁱ
  • Ref.1

    "Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission."
    Bessou C., Giugia J.-B., Franks C.J., Holden-Dye L., Segalat L.
    Neurogenetics 2:61-72(1998) [PubMed] [Europe PMC] [Abstract]

    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM A), FUNCTION, TISSUE SPECIFICITY, DISRUPTION PHENOTYPE.
• muscle cell cellular homeostasis Source: UniProtKBInferred from mutant phenotypeⁱ
  • Ref.1

    "Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission."
    Bessou C., Giugia J.-B., Franks C.J., Holden-Dye L., Segalat L.
    Neurogenetics 2:61-72(1998) [PubMed] [Europe PMC] [Abstract]

    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM A), FUNCTION, TISSUE SPECIFICITY, DISRUPTION PHENOTYPE.
• positive regulation of locomotion Source: UniProtKBInferred from mutant phenotypeⁱ
  • Ref.1

    "Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission."
    Bessou C., Giugia J.-B., Franks C.J., Holden-Dye L., Segalat L.
    Neurogenetics 2:61-72(1998) [PubMed] [Europe PMC] [Abstract]

    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM A), FUNCTION, TISSUE SPECIFICITY, DISRUPTION PHENOTYPE.
• positive regulation of synaptic transmission, cholinergic Source: WormBaseInferred from mutant phenotypeⁱ
  • Ref.1

    "Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission."
    Bessou C., Giugia J.-B., Franks C.J., Holden-Dye L., Segalat L.
    Neurogenetics 2:61-72(1998) [PubMed] [Europe PMC] [Abstract]

    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM A), FUNCTION, TISSUE SPECIFICITY, DISRUPTION PHENOTYPE.
• sarcomere organization Source: WormBase <p>Inferred from Genetic Interaction</p> <p>Used to describe "traditional" genetic interactions such as suppressors and synthetic lethals as well as other techniques such as functional complementation, rescue experiments, or inferences about a gene drawn from the phenotype of a mutation in a different gene.</p> <p>More information in the <a href="http://geneontology.org/page/guide-go-evidence-codes#igi">GO evidence code guide</a></p> Inferred from genetic interactionⁱ
  • Ref.5

    "Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans."
    Gieseler K., Grisoni K., Segalat L.
    Curr. Biol. 10:1092-1097(2000) [PubMed] [Europe PMC] [Abstract]

    Cited for: FUNCTION, DISRUPTION PHENOTYPE.
• synaptic signaling Source: GO_Central <p>Inferred from Biological aspect of Ancestor</p> <p>A type of phylogenetic evidence whereby an aspect of a descendent is inferred through the characterization of an aspect of a ancestral gene.</p> <p>More information in the <a href="http://geneontology.org/page/guide-go-evidence-codes#iba">GO evidence code guide</a></p> Inferred from biological aspect of ancestorⁱ
  • "Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."
    Gaudet P., Livstone M.S., Lewis S.E., Thomas P.D.
    Brief Bioinform 12:449-462(2011) [PubMed] [Europe PMC] [Abstract]
• synaptic transmission, cholinergic Source: UniProtKBInferred from mutant phenotypeⁱ
  • Ref.1

    "Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission."
    Bessou C., Giugia J.-B., Franks C.J., Holden-Dye L., Segalat L.
    Neurogenetics 2:61-72(1998) [PubMed] [Europe PMC] [Abstract]

    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM A), FUNCTION, TISSUE SPECIFICITY, DISRUPTION PHENOTYPE.

<p>UniProtKB Keywords constitute a <a href="http://www.uniprot.org/keywords">controlled vocabulary</a> with a hierarchical structure. Keywords summarise the content of a UniProtKB entry and facilitate the search for proteins of interest.<p><a href='/help/keywords' target='_top'>More...</a></p>Keywordsⁱ

Protein family/group databases

<p>This section provides information about the protein and gene name(s) and synonym(s) and about the organism that is the source of the protein sequence.<p><a href='/help/names_and_taxonomy_section' target='_top'>More...</a></p>Names & Taxonomyⁱ

Organism-specific databases

<p>This section provides information on the location and the topology of the mature protein in the cell.<p><a href='/help/subcellular_location_section' target='_top'>More...</a></p>Subcellular locationⁱ

• UniProt annotation
• GO - Cellular component

Keywords - Cellular componentⁱ

<p>This section provides information on the disease(s) and phenotype(s) associated with a protein.<p><a href='/help/pathology_and_biotech_section' target='_top'>More...</a></p>Pathology & Biotechⁱ

<p>This subsection of the 'Pathology and Biotech' section describes the in vivo effects caused by ablation of the gene (or one or more transcripts) coding for the protein described in the entry. This includes gene knockout and knockdown, provided experiments have been performed in the context of a whole organism or a specific tissue, and not at the single-cell level.<p><a href='/help/disruption_phenotype' target='_top'>More...</a></p>Disruption phenotypeⁱ

<p>This section describes post-translational modifications (PTMs) and/or processing events.<p><a href='/help/ptm_processing_section' target='_top'>More...</a></p>PTM / Processingⁱ

Molecule processing

Proteomic databases

PTM databases

<p>This section provides information on the expression of a gene at the mRNA or protein level in cells or in tissues of multicellular organisms.<p><a href='/help/expression_section' target='_top'>More...</a></p>Expressionⁱ

<p>This subsection of the 'Expression' section provides information on the expression of a gene at the mRNA or protein level in cells or in tissues of multicellular organisms. By default, the information is derived from experiments at the mRNA level, unless specified 'at protein level'.<br></br>Examples: <a href="http://www.uniprot.org/uniprot/P92958#expression">P92958</a>, <a href="http://www.uniprot.org/uniprot/Q8TDN4#expression">Q8TDN4</a>, <a href="http://www.uniprot.org/uniprot/O14734#expression">O14734</a><p><a href='/help/tissue_specificity' target='_top'>More...</a></p>Tissue specificityⁱ

Gene expression databases

<p>This section provides information on the quaternary structure of a protein and on interaction(s) with other proteins or protein complexes.<p><a href='/help/interaction_section' target='_top'>More...</a></p>Interactionⁱ

<p>This subsection of the <a href="http://www.uniprot.org/help/interaction%5Fsection">'Interaction'</a> section provides information about the protein quaternary structure and interaction(s) with other proteins or protein complexes (with the exception of physiological receptor-ligand interactions which are annotated in the <a href="http://www.uniprot.org/help/function%5Fsection">'Function'</a> section).<p><a href='/help/subunit_structure' target='_top'>More...</a></p>Subunit structureⁱ

<p>This subsection of the '<a href="http://www.uniprot.org/help/interaction%5Fsection">Interaction</a>' section provides information about binary protein-protein interactions. The data presented in this section are a quality-filtered subset of binary interactions automatically derived from the <a href="https://www.ebi.ac.uk/intact/">IntAct database</a>. It is updated at every <a href="http://www.uniprot.org/help/synchronization">UniProt release</a>.<p><a href='/help/binary_interactions' target='_top'>More...</a></p>Binary interactionsⁱ

GO - Molecular functionⁱ

• actin binding Source: UniProtKB-KW

Protein-protein interaction databases

<p>This section provides information on the tertiary and secondary structure of a protein.<p><a href='/help/structure_section' target='_top'>More...</a></p>Structureⁱ

3D structure databases

<p>This section provides information on sequence similarities with other proteins and the domain(s) present in a protein.<p><a href='/help/family_and_domains_section' target='_top'>More...</a></p>Family & Domainsⁱ

Domains and Repeats

Region

Compositional bias

Zinc finger

Keywords - Domainⁱ

Phylogenomic databases

Family and domain databases

<p>This section displays by default the canonical protein sequence and upon request all isoforms described in the entry. It also includes information pertinent to the sequence(s), including <a href="http://www.uniprot.org/help/sequence%5Flength">length</a> and <a href="http://www.uniprot.org/help/sequences">molecular weight</a>. The information is filed in different subsections. The current subsections and their content are listed below:<p><a href='/help/sequences_section' target='_top'>More...</a></p>Sequences (2+)ⁱ

<p>This subsection of the <a href="http://www.uniprot.org/help/sequences%5Fsection">Sequence</a> section indicates if the <a href="http://www.uniprot.org/help/canonical%5Fand%5Fisoforms">canonical sequence</a> displayed by default in the entry is complete or not.<p><a href='/help/sequence_status' target='_top'>More...</a></p>Sequence statusⁱ: Complete.

This entry has 2 described isoforms and 8 potential isoforms that are computationally mapped.Show allAlign All

        10         20         30         40         50
MLFSGASTAK PKKDEKKDKK SDRDPKNELQ EWVFVRWANH LLGTERLTDY 
        60         70         80         90        100
KSLQDGSNAI FVYQAIIGQT MAVLGNPSDD WPNVLQNIGD SKTNPQEVME 
       110        120        130        140        150
GQQKAVLSAW WQLVQFFWKN NAPVQLREEK LSEAIKQWCI EVMKSYEEID 
       160        170        180        190        200
VYDFTSSFRD GHAFNYLIHS YDRKLINLTK TAEMSAIDRI ENAFAVAEKT 
       210        220        230        240        250
WNVPRLLNPK DLHSDQLDSH SVLCYLMSLY LAMISTSKIE TELEAQQIQQ 
       260        270        280        290        300
QKVAALLASH KMLSSQPSTS SSSALQIPPQ TPPTAHHQAM LDRGKSFEQS 
       310        320        330        340        350
AEGEVRSRKS SSSSQKSGKS KKARREEQLA EFKSCIEQVL TWLLEAEDEL 
       360        370        380        390        400
TTLTQMPRVE LASVRSQFSD FESFMSSLTD SQDTVGRVLL RGQMLSNKSE 
       410        420        430        440        450
SEEEKESIGA NLHLVNTRWE ALREQAMQEQ AVLQQQIHLL QQSELDTISQ 
       460        470        480        490        500
WLDAAELEIE SFGPLAADSS QALRQIELHT KFQQKLNDFQ ETIDKLESFV 
       510        520        530        540        550
AVVDEENDAS VATLEDALSA VSVRWGHVCE WAEKRATKLD GLADLLDKTN 
       560        570        580        590        600
EVFENLSGWL AERENELMTG LKSAHHLENE EQVAQQVRRL QKTEEQLEQE 
       610        620        630        640        650
HASFVRLSQL SCELVGRLDD SNGAAANAVR LSLDSITQRW DNLVARIEEH 
       660        670        680        690        700
GKTLVKSGKA DVKQVQESQN EQKEQPASSE GLSTDTEGEE QKNQLVDKFL 
       710        720        730        740        750
LHISKLSHEL EPLQDWSEKF EVSRKKDDIR KMMNTCQEKL IQIKEQEARV 
       760        770        780        790        800
NRLQLELEHL HVAKLNARQL KRANDAFEQF AKGWARIVTK ISEAMNVLTG 
       810        820        830        840        850
QEAGGNGNGS EEAAVAAKIE QWIEAVDKVI NELSQLPVNE RRSRIDKLEQ 
       860        870        880        890        900
QLQVQDKNVG FIEKDLLKKA ILKKGLEIAG KRLAALKVEE KPVEKEEQLV 
       910        920        930        940        950
LSNSEEPEAE KHVTFVQETT EKPAPLQEPT SEAQLLEELD GPWSRVGDVV 
       960        970        980        990       1000
AIEHDLLRAK RAVDTARNSQ MSNETVEKAE TRKAEMEEKR RVTMSARSKF 
      1010       1020       1030       1040       1050
RMAEETLEEI ERNLDRLQVS DLEIADLVRG LEQEAAKLGE RVSQRKEAER 
      1060       1070       1080       1090       1100
TAEKILSMDD DEISQEIVIK TKDSTEKLIK RWNQLELDLE ENLRKAKRDQ 
      1110       1120       1130       1140       1150
DVFIQKRLRE GEEALNEIKT AIEGKRESLD AETAAENLDH LESSLDNISS 
      1160       1170       1180       1190       1200
LFGEIGSLPM DDNSREKLSK LAKAKDQITA RANEALAALT RTVSECEDFE 
      1210       1220       1230       1240       1250
KQIMLFQNWS ARIGFLLQAR KSADISAFDI PHEYHEDLGN EAELIPKLSR 
      1260       1270       1280       1290       1300
EFEEWTVKLN EMNSTATEKD DSARMREQLN HANETMAELK RKFNEFKRPK 
      1310       1320       1330       1340       1350
GFEEKLEKVI TTLSNVEMGL DDTTGIDGSE CGGALMEVRA LVRMLDGAQE 
      1360       1370       1380       1390       1400
KWKDLAENRE QLVKDRVLDE ETSKETLQKL QYAKTKSKEL YERSSTCIER 
      1410       1420       1430       1440       1450
LEDCVEMYQR LKMESDEIER FLEEMEGKLD QYAASDRPEE AEIVNELISE 
      1460       1470       1480       1490       1500
WNRNEAAMKN AEHLQRQLNE RAIKIPDDVL SLKRLRADAL KNRLNSWCRT 
      1510       1520       1530       1540       1550
IQEMSEDDES ALLEIDELHQ NLEKELKLVS DKEPSKIAEK LRFLRADRDR 
      1560       1570       1580       1590       1600
LSSRTRKLAA KNPRLAATSS DVLAGLNQKW KELEVKASAE KAPAPELRDA 
      1610       1620       1630       1640       1650
RLSSPSEQPF DKRVQELCDL FENLEAQLDF NGSPVSMVTE YQKRVENLDE 
      1660       1670       1680       1690       1700
YLDEYRPALD DTIEEGRKIA ETGRLELQTH SAIEKLDELT NRIEQVEVEL 
      1710       1720       1730       1740       1750
DKHRDKVPSL VEQHEQLKKD IDSFLLVLDV FTDRNLDDVD IAKSTRKELA 
      1760       1770       1780       1790       1800
ERDSHIVSLT SRATAIHCAL PGKGPQLHDV TLDKLRDRIE KLEARLSATE 
      1810       1820       1830       1840       1850
KKPVETVKST IPDRPEVPEE PEKSSPDRTS RSSLQLAMEA YGTATEDDSV 
      1860       1870       1880       1890       1900
ISEAVTVGQK SVDQVDPVEQ LEPVEPVEPK LEVKQLKDEA TEEEEKRTII 
      1910       1920       1930       1940       1950
LPDETEKVIE TIPAARPSAG PSEGTVAEVS TSEILKARPA QESIERTVRE 
      1960       1970       1980       1990       2000
VPVDEYEETA NISSGDELQD HKISSAVPDS ESEIASMFEV LDSIEDSHTN 
      2010       2020       2030       2040       2050
FEEFPFDYLD SADDDLKKTL LKLESCEKTL AKNEMTINIA QAENARERIT 
      2060       2070       2080       2090       2100
MLRQMALQRK DKLPKFNEEW NAMQELIQLA DALVDEAERY ESDQIPQMDR 
      2110       2120       2130       2140       2150
KSAPNVLGEL RKRVANAEGP VIDLVKKLSQ LVPRMQEDSP KSQDIRQKVY 
      2160       2170       2180       2190       2200
GIEDRFRRVG QAEGAAISKA LSSALTEPEL KLELDEVVRW CEMAEKEAAQ 
      2210       2220       2230       2240       2250
NVNSLDGDGL EKLDGRLAQF TKELQERKDD MVQLEMAKNM IIPSLKGDAH 
      2260       2270       2280       2290       2300
HDLRRNFSDT AKRVAMVRDE LSDAHKWVAT SRDTCDTFWA DIDSLEQLAR 
      2310       2320       2330       2340       2350
DVVRRANGIR MAVIYTPSRE NVEGVLRDVQ RLKMSIGDVK KRVQTANLPP 
      2360       2370       2380       2390       2400
AIKLAGKNAK RVVQVLTETA TTIADCHDIP TYLIDEMNDS GGDTTESRST 
      2410       2420       2430       2440       2450
VVEMTSVHTK QSSSSSSNKT PSAGGESDDA HTLNGDDEQS EEDQKIYSRE 
      2460       2470       2480       2490       2500
SSSTLPRGVS SLGSTGSSGV LDPVAVQLTH TRHWLHDVER DASITVDLAQ 
      2510       2520       2530       2540       2550
WQPARELWQS IQGIIDEIRL RSVHVTGAHD ASPNRQVRQQ AAQLLTEMRR 
      2560       2570       2580       2590       2600
TIENCEKRCL ILNQISDIAR QNEASRNEME LWLKSASDVI GERRVEELSE 
      2610       2620       2630       2640       2650
EVVRQELQVL ERVVEQLTER KDKMAEINSQ ANKIVDTYTK DEAHNLSHLL 
      2660       2670       2680       2690       2700
SRLNMSWTKF NDNIRIRRAV LEASLRSRRD FHSALSEFEK WLSRQEDNCS 
      2710       2720       2730       2740       2750
KLSADTSNHQ AIKDTSKRKN WTQSFKTLNA ELNAHEDVMK SVEKMGKMLA 
      2760       2770       2780       2790       2800
ESLESGNEKV ELLKRVGETT RRWTALRKTT NEIGERLEKA EQEWEKLSDG 
      2810       2820       2830       2840       2850
LADLLSWVEA KKQAIMDEQP TGGSLSAVMQ QASFVKGLQR EIESKTANYK 
      2860       2870       2880       2890       2900
STVEEAHSFL MQHDLRPKLH SPHVLDDDYE KEELANLEQR RRGLEINANC 
      2910       2920       2930       2940       2950
ERLKKNWAEL GIEVESWDKL VQHAMQRLQE LERNLAECQL HLTSSENEIE 
      2960       2970       2980       2990       3000
TMKAVEKIHL EDLKIAREET DQISKRIDEV RLFVDDVNDA AARLLAEDLK 
      3010       3020       3030       3040       3050
LDEHAKGQIE HVNKRYSTLK RAIRIRQAAV RNAASDFGPT SEHFLNQSVT 
      3060       3070       3080       3090       3100
LPWQRAISKS NLLPYYIEQT SEKTQWEHPV WVEIVKELSQ FNRVKFLAYR 
      3110       3120       3130       3140       3150
TAMKLRALQK RLCLDLVDLT LLEKAFVRLK GLSAEECPGL EGMVCALLPM 
      3160       3170       3180       3190       3200
YEALHAKYPN QVQSVSLAVD ICINFLLNLF DQSRDGIMRV LSFKIAMIVF 
      3210       3220       3230       3240       3250
SNIPLEEKYR YLFKLVSQDG HATQKQIALL LYDLIHIPRL VGESAAFGGT 
      3260       3270       3280       3290       3300
NVEPSVRSCF ETVRLAPTIS EGAFIDWVKK EPQSIVWLAV MHRLVISEST 
      3310       3320       3330       3340       3350
KHASKCNVCK MFPIIGIRYR CLTCFNCDLC QNCFFSQRTA KSHRTNHPMQ 
      3360       3370       3380       3390       3400
EYCEKTTSSD DARDFAKMIR NKFRASKRQK GYLPIDVAEE GIPLTCPPAK 
      3410       3420       3430       3440       3450
VTNQATEQMN ADTSQMTAHL AKLSAEHGGG AEHMEPVQSP LQIINQVEQL 
      3460       3470       3480       3490       3500
QRDEMDQMLH RLQFENKQLR KELEWKRGAA STMEIDRSSK RHQERHQSES 
      3510       3520       3530       3540       3550
RGGTLPLRNG RSVVSLKSTQ SQNDVMDEAK ALRLHKQRLE HRSRILEQQN 
      3560       3570       3580       3590       3600
EQLEMQLQRL KKVIDAQKQQ APLSTNSLLR GSHHQPWSPE RARSGSASTL 
      3610       3620       3630       3640       3650
DRGLIVSSRH QEQAEAAGGG AEDSSDEAGG AGGGPRGSSV GQMQNLMTAC 
      3660       3670 
DDLGKAMESL VVSVVYDSDD EEND                             

        10         20         30         40         50
MCSLLKLLKI SGKSVSDDDP IERYIKCEQC KCKRHWVEQL QRDEMDQMLH 
        60         70         80         90        100
RLQFENKQLR KELEWKRGAA STMEIDRSSK RHQERHQSES RGGTLPLRNG 
       110        120        130        140        150
RSVVSLKSTQ SQNDVMDEAK ALRLHKQRLE HRSRILEQQN EQLEMQLQRL 
       160        170        180        190        200
KKVIDAQKQQ APLSTNSLLR GSHHQPWSPE RARSGSASTL DRGLIVSSRH 
       210        220        230        240        250
QEQAEAAGGG AEDSSDEAGG AGGGPRGSSV GQMQNLMTAC DDLGKAMESL 
       260 
VVSVVYDSDD EEND                                        

Alternative sequence

Sequence databases

Genome annotation databases

Keywords - Coding sequence diversityⁱ

<p>This section provides links to proteins that are similar to the protein sequence(s) described in this entry at different levels of sequence identity thresholds (100%, 90% and 50%) based on their membership in UniProt Reference Clusters (<a href="http://www.uniprot.org/help/uniref">UniRef</a>).<p><a href='/help/similar_proteins_section' target='_top'>More...</a></p>Similar proteinsⁱ

• 100% Identity
• 90% Identity
• 50% Identity

<p>This section is used to point to information related to entries and found in data collections other than UniProtKB.<p><a href='/help/cross_references_section' target='_top'>More...</a></p>Cross-referencesⁱ

Sequence databases

3D structure databases

Protein-protein interaction databases

Protein family/group databases

PTM databases

Proteomic databases

Genome annotation databases

Organism-specific databases

Phylogenomic databases

Miscellaneous databases

Gene expression databases

Family and domain databases

<p>This section provides general information on the entry.<p><a href='/help/entry_information_section' target='_top'>More...</a></p>Entry informationⁱ

<p>This section contains any relevant information that doesn't fit in any other defined sections<p><a href='/help/miscellaneous_section' target='_top'>More...</a></p>Miscellaneousⁱ

Keywords - Technical termⁱ

Documents

1. Caenorhabditis elegans
   Caenorhabditis elegans: entries, gene names and cross-references to WormBase