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WormBase Tree Display for Gene: WBGene00020509

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Name Class

WBGene00020509SMapS_parentSequenceT14F9
IdentityVersion2
NameCGC_namehex-1Person_evidenceWBPerson2099
Sequence_nameT14F9.3
Molecular_nameT14F9.3
T14F9.3.1
CE07499
T14F9.3.2
Other_nameCELE_T14F9.3Accession_evidenceNDBBX284606
Public_namehex-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
219 Jul 2007 09:29:24WBPerson2970Name_changeCGC_namehex-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhex
Allele (68)
StrainWBStrain00002884
In_clusterconserved_RDE-1_cluster
RNASeq_FPKM (74)
GO_annotation (21)
Ortholog (41)
Structured_descriptionConcise_descriptionhex-1 encodes a beta-N-acetylhexosaminidase that is orthologous to the human gene CERVICAL CANCER PROTO-ONCOGENE 7 (HEXB; OMIM:606873), which when mutated leads to disease.Paper_evidenceWBPaper00030867
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated23 Jul 2007 00:00:00
Automated_descriptionEnables beta-N-acetylhexosaminidase activity. Involved in carbohydrate metabolic process. Predicted to be located in lysosome and membrane. Expressed in coelomocyte and pharyngeal neurons. Human ortholog(s) of this gene implicated in Sandhoff disease; Tay-Sachs disease; and spinal muscular atrophy. Is an ortholog of human HEXA (hexosaminidase subunit alpha) and HEXB (hexosaminidase subunit beta).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:12377Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4879)
DOID:3323Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4879)
DOID:3320Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4878)
Molecular_infoCorresponding_CDST14F9.3
Corresponding_transcriptT14F9.3.1
T14F9.3.2
Other_sequence (41)
Associated_featureWBsf655166
WBsf662510
WBsf662511
WBsf1004268
WBsf235376
Experimental_infoRNAi_resultWBRNAi00053327Inferred_automaticallyRNAi_primary
WBRNAi00018714Inferred_automaticallyRNAi_primary
WBRNAi00035568Inferred_automaticallyRNAi_primary
Expr_pattern (8)
Drives_constructWBCnstr00003403
WBCnstr00004955
WBCnstr00025086
Construct_productWBCnstr00025086
Microarray_resultsSMD_T14F9.3
173287_s_at
192747_at
A_12_P106940
A_12_P157825
Aff_T14F9.3
GPL13394_WBGene00020509
GPL13914_T14F9.3
GPL14144_T14F9.3_1157-1216_0.921_8_B
GPL14144_T14F9.3_1305-1364_0.921_7_A
GPL14144_T14F9.3_818-877_0.898_17_C
GPL19516_CGZ0035178
GPL21109_T14F9.3
GPL3518_CE07499
GPL8304_CE_WBGene00020509_A
GPL8304_CE_WBGene00020509_B
GPL8304_CE_WBGene00020509_C
GPL8673_T14F9_3P00339
GPL8673_T14F9_3P00946
GPL8673_T14F9_3P01415
GPL9450_T14F9.3
cea2.c.47924
Expression_cluster (276)
Interaction (124)
Map_infoMapXPosition-16.3239Error0.135409
PositivePositive_cloneT14F9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00030867
WBPaper00038491
WBPaper00055090
WBPaper00059755
WBPaper00062715
WBPaper00065036
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