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WormBase Tree Display for Gene: WBGene00006915

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Name Class

WBGene00006915SMapS_parentSequenceCHROMOSOME_II
IdentityVersion1
NameCGC_namevha-6
Sequence_nameVW02B12L.1
Molecular_nameVW02B12L.1
VW02B12L.1.1
CE18980
Other_nameCELE_VW02B12L.1Accession_evidenceNDBBX284602
Public_namevha-6
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:43WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classvha
Allele (54)
Legacy_information[Pujol N] vha-6 is expressed only in the intestine, from the embryonic coma stage through larvae and adult
StrainWBStrain00036524
RNASeq_FPKM (74)
GO_annotation (17)
Ortholog (58)
ParalogWBGene00006768Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006914Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006916Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_description (2)
Disease_infoPotential_modelDOID:0070390Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:865)
DOID:0110942Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11647)
DOID:14219Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:866)
DOID:0112171Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18481)
EFO:MONDO:0015827Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:866)
DOID:0070134Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18481)
Molecular_infoCorresponding_CDSVW02B12L.1
Corresponding_transcriptVW02B12L.1.1
Other_sequenceAB055111
EX008139.1
FN601335.1
Oden_isotig12989
AS05322
FD513973.1
EX558568.1
PPC02052_1
Tcir_isotig07492
ACC04350_1
Tcir_isotig29012
Dviv_isotig35691
SR02674
FG973358.1
Name_isotig03156
MJ04859
FC543463.1
Dviv_isotig28706
EX012282.1
FC541220.1
PTC01014_1
CJC00902_1
EX008515.1
JO472469.1
ES561315.1
NAC00347_1
SRC01652_1
Tcir_isotig16492
HBC21651_1
FC543579.1
Tcol_isotig13075
FC543557.1
Acan_isotig18969
EY465731.1
BG467540.1
ASC01106_1
ASC24020_1
Hbac_isotig03389
FC810282.1
Hbac_isotig06054
JI171090.1
JI220521.1
JI174902.1
EY469248.1
PPC17889_1
SRC01750_1
ACC12501_1
FC815931.1
ACC15048_1
Dviv_isotig26420
AS08080
FC815666.1
Acan_isotig07945
PT01196
HC00751
PPC13084_1
HCC04093_1
CBC03657_1
FC810508.1
HBC14954_1
FC541171.1
JO472504.1
Name_isotig06322
CSC00688_1
Oden_isotig26768
BU606334.1
Oden_isotig12990
AS01642
PP02479
FC540466.1
MJC03988_1
Associated_featureWBsf650573
WBsf650574
WBsf989758
WBsf1013237
WBsf223933
Experimental_infoRNAi_result (55)
Expr_patternExpr851
Expr2404
Expr2407
Expr13465
Expr1029215
Expr1032932
Expr1158019
Expr2017992
Expr2036128
Drives_construct (205)
Construct_productWBCnstr00013297
WBCnstr00016253
WBCnstr00038389
AntibodyWBAntibody00000406
Microarray_results (20)
Expression_cluster (230)
Interaction (123)
Map_infoMapIIPosition3.46558Error0.000297
PositivePositive_cloneVW02B12LInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (28)
RemarkSequence From: Pujol Nathalie via ACEDB feedback page <pujol@lgpd.univ-mrs.fr>
Map 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