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WormBase Tree Display for Gene: WBGene00006498

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Name Class

WBGene00006498SMapS_parentSequenceCHROMOSOME_III
IdentityVersion4
NameCGC_nameten-1Person_evidenceWBPerson104
Sequence_nameR13F6.4
Molecular_name (16)
Other_nametag-152Person_evidenceWBPerson201
mnm-5Paper_evidenceWBPaper00036313
Person_evidenceWBPerson488
CELE_R13F6.4Accession_evidenceNDBBX284603
Public_nameten-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:40WBPerson1971EventImportedInitial conversion from geneace
226 Jul 2005 11:46:16WBPerson2970Name_changeCGC_nameten-1
Other_nametag-152
320 Oct 2005 09:04:04WBPerson1867EventAcquires_mergeWBGene00017903
417 Aug 2010 12:12:13WBPerson2970EventAcquires_mergeWBGene00003383
Name_changeOther_namemnm-1
Acquires_mergeWBGene00003383
WBGene00017903
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classten
Allele (374)
StrainWBStrain00003335
WBStrain00003336
WBStrain00031159
WBStrain00035839
WBStrain00050786
RNASeq_FPKM (74)
GO_annotation (38)
Ortholog (54)
ParalogWBGene00011326Caenorhabditis elegansFrom_analysisPanther
WBGene00017892Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00018237Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionten-1 encodes a type II transmembrane protein containing EGF-like repeats that is the C. elegans ortholog of Drosophila Ten-m/Odz and vertebrate teneurins (OMIM:300588); in C. elegans, TEN-1 is required for proper development of the gonadal and pharyngeal basement membranes and for proper axonal placement and hypodermal morphogenesis; ten-1 and phy-1 act in parallel influencing the connection between epidermis and muscle during embryonic development; TEN-1 acts as an epidermal receptor for the BM collagens modified by PHY-1 and secreted by the muscle cells; loss of P4H function in ten-1 null mutants results in embryonic lethality due to arrest during late elongation with morphological defects; ten-1; phy-1 embryos have defects in epidermal development and body wall muscles due to basement membrane defects in arrested embryos; TEN-1 is expressed in the embryo and in multiple tissues during postembryonic development including the somatic gonad founder cells Z1 and Z4 and their descendants, as well as in six marginal cells and the M2 neurons in the pharynx; in the embryo, ten-1 expression overlaps with that of lat-1 in the dorsal left epidermoblasts; as ten-1 and lat-1 also display genetic interactions during embryonic development, the overlapping expression patterns suggest that these two genes have overlapping functions during embryogenesis.Paper_evidenceWBPaper00004588
WBPaper00006025
WBPaper00025239
WBPaper00032026
WBPaper00036313
WBPaper00039988
WBPaper00041503
Curator_confirmedWBPerson12884
WBPerson1843
WBPerson567
Date_last_updated22 Oct 2012 00:00:00
Automated_descriptionInvolved in several processes, including axon development; body morphogenesis; and gonad development. Located in nucleus and plasma membrane. Expressed in several structures, including body muscle cell; gonad; hypodermis; interfacial epithelial cell; and neurons. Human ortholog(s) of this gene implicated in essential tremor 5. Is an ortholog of human TENM2 (teneurin transmembrane protein 2) and TENM3 (teneurin transmembrane protein 3).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelEFO:MONDO:0000170Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29944)
DOID:0111432Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29945)
DOID:9975Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29944)
Molecular_infoCorresponding_CDSR13F6.4a
R13F6.4c
R13F6.4d
R13F6.4e
R13F6.4f
Corresponding_CDS_historyR13F6.4:wp82
R13F6.4a:wp229
R13F6.4b:wp142
R13F6.4d:wp193
Corresponding_transcriptR13F6.4a.1
R13F6.4a.2
R13F6.4c.1
R13F6.4d.1
R13F6.4e.1
R13F6.4f.1
Other_sequenceJI163882.1
CBC07315_1
CR01340
CRC08247_1
CRC01406_1
CR09660
CR08459
Associated_featureWBsf645290
WBsf645293
WBsf645294
WBsf658489
WBsf658522
WBsf659112
WBsf659113
WBsf659114
WBsf659115
WBsf659116
WBsf659117
WBsf659118
WBsf659119
WBsf659120
WBsf659121
WBsf659122
WBsf659123
WBsf659124
WBsf659125
WBsf659126
WBsf992865
WBsf992866
WBsf992867
WBsf992868
WBsf992869
WBsf992870
WBsf992871
WBsf992872
WBsf992873
WBsf992874
WBsf992875
WBsf992876
WBsf992877
WBsf992878
WBsf992879
WBsf992880
WBsf992881
WBsf992882
WBsf992883
WBsf992884
WBsf992885
WBsf1015158
WBsf1015159
WBsf1015160
WBsf1015161
WBsf225156
WBsf225157
WBsf225158
Experimental_infoRNAi_result (18)
Expr_pattern (14)
Drives_construct (11)
Construct_productWBCnstr00005422
WBCnstr00008913
WBCnstr00008960
WBCnstr00034335
AntibodyWBAntibody00000932
WBAntibody00000933
Microarray_results (38)
Expression_cluster (152)
Interaction (12)
Map_infoMapIIIPosition-0.935519Error0.002543
PositivePositive_cloneR13F6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4762
4976
Pseudo_map_position
Reference (21)
RemarkMap position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene