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WormBase Tree Display for Gene: WBGene00001399

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Name Class

WBGene00001399SMapS_parentSequenceF10D2
IdentityVersion1
NameCGC_namefat-7
Sequence_nameF10D2.9
Molecular_nameF10D2.9
F10D2.9.1
CE09320
Other_nameCELE_F10D2.9Accession_evidenceNDBBX284605
Public_namefat-7
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfat
Allele (42)
StrainWBStrain00004020
WBStrain00004021
WBStrain00004022
WBStrain00008410
WBStrain00008411
RNASeq_FPKM (74)
GO_annotation (21)
Ortholog (59)
ParalogWBGene00001397Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00001398Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionfat-7 encodes an essential delta-9 fatty acid desaturase that is required for the synthesis of monounsaturated fatty acids; fat-7 can substitute for the functions of the other two fatty acid desaturases, fat-5 and fat-6; RNA interference has shown that fat-7 is required for viability and normal growth.Paper_evidenceWBPaper00004149
WBPaper00004424
WBPaper00005754
WBPaper00006113
WBPaper00013538
WBPaper00013550
Curator_confirmedWBPerson324
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables stearoyl-CoA 9-desaturase activity. Involved in fatty acid biosynthetic process and post-embryonic development. Acts upstream of or within intracellular oxygen homeostasis and response to hypoxia. Predicted to be located in endoplasmic reticulum membrane. Expressed in intestinal cell. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 79. Is an ortholog of human SCD (stearoyl-CoA desaturase) and SCD5 (stearoyl-CoA desaturase 5).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_modelDOID:0112160Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:21088)
Molecular_infoCorresponding_CDSF10D2.9
Corresponding_transcriptF10D2.9.1
Other_sequence (60)
Associated_featureWBsf019173
WBsf019174
WBsf019175
WBsf978978
WBsf233910
WBsf233911
Experimental_infoRNAi_result (54)
Expr_patternChronogram631
Expr4292
Expr4571
Expr5716
Expr13449
Expr16083
Expr1021466
Expr1148206
Expr2011440
Expr2029678
Drives_constructWBCnstr00004076
WBCnstr00009389
WBCnstr00011890
WBCnstr00016671
WBCnstr00020551
WBCnstr00036971
WBCnstr00042754
Construct_productWBCnstr00011890
WBCnstr00016671
WBCnstr00020551
WBCnstr00036971
WBCnstr00038737
Microarray_results (18)
Expression_cluster (383)
Interaction (289)
WBProcessWBbiopr:00000121
Map_infoMapVPosition0.613044Error0.000716
PositivePositive_cloneF10D2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4303
4307
Pseudo_map_position
ReferenceWBPaper00004149
WBPaper00005976
WBPaper00006160
WBPaper00018784
WBPaper00024086
WBPaper00024111
WBPaper00025114
WBPaper00026097
WBPaper00026349
WBPaper00026800
WBPaper00027365
WBPaper00027707
WBPaper00027749
WBPaper00029195
WBPaper00029226
WBPaper00029292
WBPaper00030454
WBPaper00031804
WBPaper00032634
WBPaper00032661
WBPaper00033126
WBPaper00033136
WBPaper00033382
WBPaper00033689
WBPaper00033728
WBPaper00033922
WBPaper00034335
WBPaper00034497
WBPaper00034498
WBPaper00034502
WBPaper00034504
WBPaper00035452
WBPaper00035560
WBPaper00036042
WBPaper00036474
WBPaper00036476
WBPaper00037402
WBPaper00037414
WBPaper00037502
WBPaper00038126
WBPaper00038491
WBPaper00038832
WBPaper00038982
WBPaper00039262
WBPaper00039723
WBPaper00039810
WBPaper00040208
WBPaper00040386
WBPaper00040706
WBPaper00040998
WBPaper00041973
WBPaper00042257
WBPaper00042856
WBPaper00042964
WBPaper00043167
WBPaper00044077
WBPaper00044578
WBPaper00044659
WBPaper00046830
WBPaper00047716
WBPaper00048987
WBPaper00049011
WBPaper00049740
WBPaper00053474
WBPaper00053788
WBPaper00055090
WBPaper00055256
WBPaper00055800
WBPaper00056739
WBPaper00056988
WBPaper00057086
WBPaper00057158
WBPaper00058278
WBPaper00059111
WBPaper00059136
WBPaper00059578
WBPaper00059658
WBPaper00059949
WBPaper00059977
WBPaper00059995
WBPaper00060060
WBPaper00060204
WBPaper00060264
WBPaper00060399
WBPaper00060713
WBPaper00060760
WBPaper00060893
WBPaper00060921
WBPaper00061413
WBPaper00061572
WBPaper00061746
WBPaper00061861
WBPaper00062322
WBPaper00062456
WBPaper00062463
WBPaper00062492
WBPaper00062709
WBPaper00062858
WBPaper00062990
WBPaper00063813
WBPaper00063942
WBPaper00064071
WBPaper00064097
WBPaper00064255
WBPaper00064284
WBPaper00064498
WBPaper00064516
WBPaper00064539
WBPaper00064592
WBPaper00064661
WBPaper00064721
WBPaper00064731
WBPaper00064763
WBPaper00064820
WBPaper00064847
WBPaper00064960
WBPaper00064979
WBPaper00065081
WBPaper00065123
WBPaper00065133
WBPaper00065597
WBPaper00065695
WBPaper00065727
WBPaper00065784
WBPaper00065847
WBPaper00065859
WBPaper00065904
WBPaper00065942
WBPaper00066260
WBPaper00066300
PictureWBPicture0000013088
WBPicture0000013096
WBPicture0000013098
Remarksequence connection from [Watts J]
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