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WormBase Tree Display for Gene: WBGene00008571

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Name Class

WBGene00008571SMapS_parentSequenceF08B12
IdentityVersion3
NameCGC_nameprmn-1Person_evidenceWBPerson691
Sequence_nameF08B12.1
Molecular_nameF08B12.1
F08B12.1.1
CE03162
Other_nameCELE_F08B12.1Accession_evidenceNDBBX284606
Public_nameprmn-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:49WBPerson1971EventImportedInitial conversion from CDS class of WS125
211 Dec 2012 14:02:14WBPerson2970Name_changeCGC_nameprmn-1
302 Mar 2018 10:40:21WBPerson4025EventSplit_intoWBGene00303052
Split_intoWBGene00303052
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classprmn
Allele (110)
StrainWBStrain00036390
RNASeq_FPKM (74)
GO_annotation00063780
00063781
00116485
Ortholog (40)
Structured_descriptionConcise_descriptionprmn-1 is orthologous to the human gene Prominin1 (PROML1); Prominin1 is a conserved glycoprotein and a member of the pentaspan transmembrane glycoproteins (5-transmembrane, 5-TM).Curator_confirmedWBPerson324
WBPerson1823
WBPerson567
Date_last_updated04 Nov 2013 00:00:00
Automated_descriptionPredicted to be located in membrane. Human ortholog(s) of this gene implicated in cone-rod dystrophy 12; retinal macular dystrophy; and retinitis pigmentosa 41. Is an ortholog of human PROM1 (prominin 1) and PROM2 (prominin 2).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:0110376Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9454)
DOID:0111019Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9454)
DOID:0070438Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9454)
Molecular_infoCorresponding_CDSF08B12.1
Corresponding_CDS_historyF08B12.1a:wp264
F08B12.1b:wp264
Corresponding_transcriptF08B12.1.1
Other_sequence (14)
Associated_feature (12)
Experimental_infoRNAi_resultWBRNAi00030628Inferred_automaticallyRNAi_primary
WBRNAi00012863Inferred_automaticallyRNAi_primary
WBRNAi00043961Inferred_automaticallyRNAi_primary
Expr_patternExpr1012828
Expr1033735
Expr1147935
Expr2015097
Expr2033334
Drives_constructWBCnstr00032867
Construct_productWBCnstr00032867
Microarray_results (20)
Expression_cluster (171)
InteractionWBInteraction000123134
WBInteraction000123135
WBInteraction000355285
WBInteraction000459227
WBInteraction000580600
Map_infoMapXPosition3.47275
PositivePositive_cloneF08B12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00026601
WBPaper00038491
WBPaper00042780
WBPaper00055090
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