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WormBase Tree Display for Gene: WBGene00006742

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Name Class

WBGene00006742SMapS_parentSequenceCHROMOSOME_X
IdentityVersion1
NameCGC_nameunc-2Person_evidenceWBPerson261
Sequence_nameT02C5.5
Molecular_name (45)
Other_nameCELE_T02C5.5Accession_evidenceNDBBX284606
Public_nameunc-2
DB_infoDatabaseAceViewgeneXD330
WormQTLgeneWBGene00006742
WormFluxgeneWBGene00006742
OMIMdisease141500
gene601011
601013
NDBlocus_tagCELE_T02C5.5
PanthergeneCAEEL|WormBase=WBGene00006742|UniProtKB=A0A3B1E663
familyPTHR45628
NCBIgene180570
RefSeqproteinNM_001348590.4
NM_001348592.5
NM_001348589.4
NM_001348588.4
NM_001368494.4
NM_001348593.4
NM_001348594.5
NM_001348597.2
NM_001348591.4
NM_001368497.5
NM_001348595.4
NM_001368495.4
NM_001348596.5
NM_171638.3
NM_001368496.4
TrEMBLUniProtAcc (15)
UniProt_GCRPUniProtAccA0A3B1E663
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:41WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_info (11)
Disease_infoExperimental_modelDOID:6364Homo sapiensPaper_evidenceWBPaper00006272
Accession_evidenceOMIM141500
Curator_confirmedWBPerson324
Date_last_updated14 Apr 2014 00:00:00
Potential_modelDOID:10024Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1388)
DOID:0080454Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1388)
DOID:0050956Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1388)
DOID:0112205Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1392)
DOID:2377Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1389)
DOID:0111181Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1388)
DOID:0050214Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1389)
DOID:0050990Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1388)
DOID:4724Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1389)
DOID:6364Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1388)
Disease_relevanceMutations in the human calcium channel CACNA1A (Calcium channel, voltage-dependent, P/Q type, alpha-1A subunit) are associated with Episodic ataxia (type 2), which affects the nervous system, resulting in migraines, vision and speech defects, and muscle weakness; mutations in CACNA1A also cause Spinocerebellar ataxia (type 6), a progressive movement disorder; voltage dependent calcium channels mediate calcium entry into cells and are involved in several calcium dependent processes; genetic studies in elegans show that unc-2, the ortholog of CACNA1A, negatively modulates a transforming growth factor (TGF)-beta pathway to affect certain phenotypes like movement, and for the normal accumulation of serotonin levels; further, unc-2 dependent inhibition of the TGF-beta pathway regulates the transcriptional expression of trytophan hydroxylase (tph-1) in serotonergic neurons under stress conditions like starvation and raised temperature; a construct expressing human CACNA1A can substitute for unc-2 function in elegans.Homo sapiensPaper_evidenceWBPaper00006272
Accession_evidenceOMIM601011
Curator_confirmedWBPerson324
Date_last_updated14 Apr 2014 00:00:00
Models_disease_in_annotationWBDOannot00000025
Molecular_info (5)
Experimental_infoRNAi_result (18)
Expr_pattern (13)
Drives_constructWBCnstr00003100
WBCnstr00003101
WBCnstr00004845
WBCnstr00004847
WBCnstr00038221
Construct_productWBCnstr00005852
WBCnstr00005853
WBCnstr00005854
WBCnstr00020432
WBCnstr00022471
WBCnstr00023025
WBCnstr00023027
Microarray_results (47)
Expression_cluster (201)
Interaction (139)
Anatomy_functionWBbtf0544
WBbtf0547
WBbtf0550
Map_infoMapXPosition-13.7946Error0.063386
Well_ordered
PositivePositive_cloneT02C5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point145
153
154
155
156
157
3151
4456
4457
7099
Multi_point (28)
Pos_neg_data (23)
Landmark_gene
ReferenceWBPaper00000031
WBPaper00000164
WBPaper00000608
WBPaper00001477
WBPaper00001709
WBPaper00001722
WBPaper00001852
WBPaper00002074
WBPaper00002168
WBPaper00002297
WBPaper00002487
WBPaper00002590
WBPaper00002756
WBPaper00002824
WBPaper00002832
WBPaper00003024
WBPaper00003038
WBPaper00003300
WBPaper00003760
WBPaper00003764
WBPaper00003955
WBPaper00004361
WBPaper00005102
WBPaper00005686
WBPaper00005734
WBPaper00005753
WBPaper00005799
WBPaper00006005
WBPaper00006049
WBPaper00006052
WBPaper00006076
WBPaper00006103
WBPaper00006167
WBPaper00006272
WBPaper00006296
WBPaper00006384
WBPaper00006402
WBPaper00006434
WBPaper00010480
WBPaper00010908
WBPaper00010992
WBPaper00011094
WBPaper00011099
WBPaper00014210
WBPaper00014234
WBPaper00014761
WBPaper00014772
WBPaper00014841
WBPaper00014842
WBPaper00014959
WBPaper00014960
WBPaper00015004
WBPaper00015440
WBPaper00015459
WBPaper00015628
WBPaper00016359
WBPaper00016388
WBPaper00016418
WBPaper00016621
WBPaper00016714
WBPaper00016926
WBPaper00017046
WBPaper00017112
WBPaper00017152
WBPaper00017175
WBPaper00017182
WBPaper00017184
WBPaper00017304
WBPaper00017365
WBPaper00017383
WBPaper00017406
WBPaper00017412
WBPaper00017428
WBPaper00018051
WBPaper00018323
WBPaper00018338
WBPaper00018918
WBPaper00019016
WBPaper00019070
WBPaper00019209
WBPaper00019229
WBPaper00019278
WBPaper00021934
WBPaper00022084
WBPaper00022149
WBPaper00022177
WBPaper00022459
WBPaper00022530
WBPaper00022744
WBPaper00022821
WBPaper00022843
WBPaper00022945
WBPaper00022963
WBPaper00023702
WBPaper00023731
WBPaper00023984
WBPaper00024131
WBPaper00024295
WBPaper00024600
WBPaper00024867
WBPaper00024990
WBPaper00025467
WBPaper00026068
WBPaper00026126
WBPaper00026194
WBPaper00026618
WBPaper00026667
WBPaper00026734
WBPaper00026866
WBPaper00026981
WBPaper00026988
WBPaper00027180
WBPaper00027274
WBPaper00027304
WBPaper00027305
WBPaper00027615
WBPaper00027624
WBPaper00027747
WBPaper00028105
WBPaper00028187
WBPaper00028258
WBPaper00028340
WBPaper00028384
WBPaper00028433
WBPaper00028808
WBPaper00028850
WBPaper00029015
WBPaper00029021
WBPaper00029025
WBPaper00029334
WBPaper00029404
WBPaper00029410
WBPaper00030291
WBPaper00030337
WBPaper00031000
WBPaper00031175
WBPaper00031254
WBPaper00031915
WBPaper00031982
WBPaper00032122
WBPaper00032389
WBPaper00032687
WBPaper00032811
WBPaper00032896
WBPaper00033037
WBPaper00034089
WBPaper00035163
WBPaper00035989
WBPaper00037330
WBPaper00037332
WBPaper00037339
WBPaper00038491
WBPaper00038566
WBPaper00039244
WBPaper00039245
WBPaper00039865
WBPaper00039901
WBPaper00040141
WBPaper00040144
WBPaper00040284
WBPaper00042167
WBPaper00042396
WBPaper00042931
WBPaper00043400
WBPaper00043415
WBPaper00043908
WBPaper00044263
WBPaper00045955
WBPaper00045968
WBPaper00046703
WBPaper00047904
WBPaper00048069
WBPaper00048388
WBPaper00049114
WBPaper00049806
WBPaper00051165
WBPaper00052786
WBPaper00053608
WBPaper00055090
WBPaper00057024
WBPaper00057095
WBPaper00060930
WBPaper00061313
WBPaper00061401
WBPaper00061408
WBPaper00061654
WBPaper00063130
WBPaper00063570
WBPaper00063852
WBPaper00063884
WBPaper00063950
WBPaper00064058
WBPaper00064165
WBPaper00064195
WBPaper00064506
WBPaper00065040
WBPaper00065118
WBPaper00065262
WBPaper00065342
WBPaper00065360
WBPaper00066029
MethodGene