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WormBase Tree Display for Gene: WBGene00003890

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Name Class

WBGene00003890SMapS_parentSequenceT20H4
IdentityVersion1
NameCGC_nameosm-10Person_evidenceWBPerson242
Sequence_nameT20H4.1
Molecular_nameT20H4.1a
T20H4.1a.1
CE00750
T20H4.1b
CE51605
T20H4.1b.1
Other_nameCELE_T20H4.1Accession_evidenceNDBBX284603
Public_nameosm-10
DB_infoDatabaseAceViewgene3I337
WormQTLgeneWBGene00003890
WormFluxgeneWBGene00003890
OMIMdisease256000
gene602141
NDBlocus_tagCELE_T20H4.1
NCBIgene191740
RefSeqproteinNM_001330924.2
NM_066197.7
TrEMBLUniProtAccA0A168H2S6
Q22622
UniProt_GCRPUniProtAccQ22622
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classosm
Allele (30)
Legacy_information[C.elegansII] n1602 : specifically defective in osmotic avoidance; normal chemotaxis; normal garlic avoidance; normal nose touch response. NA1. Cloned: cosmid rescue [Bargmann et al. 1990; CX, KP]
StrainWBStrain00008277
WBStrain00008292
WBStrain00008293
WBStrain00008294
WBStrain00029473
WBStrain00027082
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (22)
Structured_descriptionConcise_descriptionosm-10 encodes a novel protein conserved amongst several Caenorhabditis species; osm-10 activity is required for normal osmosensory signaling in the ASH sensory neuron; in regulating ASH-mediated osmosensation, osm-10 interacts genetically with eos-1 and eos-2; OSM-10 is expressed in the ASH, ASI, PHA, and PHB sensory neurons beginning just prior to hatching and continuing through larval and adult stages; OSM-10 localizes to cell bodies, sensory processes, and axons.Paper_evidenceWBPaper00003408
Curator_confirmedWBPerson1843
Date_last_updated25 Sep 2006 00:00:00
Automated_descriptionEnables osmosensor activity. Involved in osmosensory signaling pathway. Located in axon; cytoplasm; and neuronal cell body.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_infoDisease_relevanceMutations in the human NADH-Ubiquinone oxidoreductase Fe-S protein 8 (NDUFS8; orthologous to elegans T20H4.1), are associated with Leigh syndrome, which is an an early-onset progressive neurodegenerative disorder, characterized by progressive loss of mental and movement abilities (psychomotor regression) and typically results in death within a couple of years, usually due to respiratory failure.Homo sapiensAccession_evidenceOMIM256000
602141
Curator_confirmedWBPerson324
Date_last_updated15 Jun 2012 00:00:00
Molecular_infoCorresponding_CDST20H4.1a
T20H4.1b
Corresponding_transcriptT20H4.1a.1
T20H4.1b.1
Associated_featureWBsf645329
WBsf225227
WBsf225228
WBsf225229
Experimental_infoRNAi_resultWBRNAi00035727Inferred_automaticallyRNAi_primary
WBRNAi00053670Inferred_automaticallyRNAi_primary
WBRNAi00018934Inferred_automaticallyRNAi_primary
WBRNAi00005588Inferred_automaticallyRNAi_primary
WBRNAi00065896Inferred_automaticallyRNAi_primary
Expr_patternChronogram614
Expr515
Expr1266
Expr6725
Expr15400
Expr1022236
Expr1031833
Expr1157225
Expr2014639
Expr2032872
Drives_construct (17)
Construct_productWBCnstr00012411
WBCnstr00022367
WBCnstr00035810
AntibodyWBAntibody00000213
Microarray_results (19)
Expression_cluster (104)
Interaction (14)
Map_infoMapIIIPosition-0.764685Error0.000739
Well_ordered
PositivePositive_cloneT20H4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point3719
Multi_point1363
4042
4043
4146
Pos_neg_data3720
3721
Reference (39)
MethodGene