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WormBase Tree Display for Gene: WBGene00016415

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Name Class

WBGene00016415SMapS_parentSequenceC34F11
IdentityVersion2
NameCGC_nameampd-1Person_evidenceWBPerson10610
Sequence_nameC34F11.3
Molecular_name (12)
Other_nameCELE_C34F11.3Accession_evidenceNDBBX284602
Public_nameampd-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
227 Jun 2014 15:53:55WBPerson2970Name_changeCGC_nameampd-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classampd
AlleleWBVar00171934
WBVar00171935
WBVar00171936
WBVar01499702
WBVar00238007
WBVar01498435
WBVar02124677
WBVar02156332
WBVar00316209
WBVar00316210
WBVar00275984
WBVar00223652
WBVar00223653
WBVar00223655
WBVar00223657
WBVar00223658
WBVar00223659
WBVar00730649
WBVar00730650
WBVar00730651
WBVar00730652
WBVar00730653
WBVar00730654
WBVar00730655
WBVar00730656
WBVar00730657
WBVar00730658
WBVar00730659
WBVar00730660
WBVar00730661
WBVar00730662
WBVar00730663
WBVar00730664
WBVar00730665
WBVar02129909
WBVar00730666
WBVar00730667
WBVar02129910
WBVar00730668
WBVar00730669
WBVar02122540
WBVar00730670
WBVar00730671
WBVar00730672
WBVar00730673
WBVar00253862
WBVar00730674
WBVar00730675
WBVar00730676
WBVar01685322
WBVar00730677
WBVar00730678
WBVar00730679
WBVar00730680
WBVar00730681
WBVar00730682
WBVar01891699
WBVar00365683
WBVar00365684
WBVar00365685
WBVar00365686
WBVar00365687
WBVar00365688
WBVar00365689
WBVar00365690
WBVar00365691
WBVar00365692
WBVar00365693
WBVar00365694
WBVar00365695
WBVar01372600
WBVar01372611
WBVar01493966
WBVar00103855
WBVar01248951
WBVar00171932
WBVar02033229
WBVar00171933
StrainWBStrain00051109
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (49)
Structured_descriptionAutomated_descriptionPredicted to enable AMP deaminase activity. Predicted to be involved in AMP metabolic process and IMP biosynthetic process. Predicted to be located in cytosol. Human ortholog(s) of this gene implicated in several diseases, including congestive heart failure; hereditary spastic paraplegia 63; and pontocerebellar hypoplasia type 9. Is an ortholog of human AMPD2 (adenosine monophosphate deaminase 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:6000Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:468)
DOID:0060278Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:469)
DOID:0110814Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:469)
DOID:3393Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:468)
Molecular_infoCorresponding_CDSC34F11.3a
C34F11.3b
C34F11.3c
C34F11.3d
Corresponding_CDS_historyC34F11.3a:wp88
C34F11.3a:wp214
C34F11.3b:wp88
C34F11.3b:wp214
C34F11.3c:wp214
Corresponding_transcriptC34F11.3a.1
C34F11.3b.1
C34F11.3c.1
C34F11.3d.1
Other_sequence (78)
Associated_featureWBsf644169
WBsf654864
WBsf716685
WBsf987815
WBsf987816
WBsf987817
WBsf1012193
WBsf1012194
WBsf221244
Experimental_infoRNAi_resultWBRNAi00041909Inferred_automaticallyRNAi_primary
WBRNAi00076196Inferred_automaticallyRNAi_primary
WBRNAi00041910Inferred_automaticallyRNAi_primary
WBRNAi00011616Inferred_automaticallyRNAi_primary
WBRNAi00024736Inferred_automaticallyRNAi_primary
WBRNAi00027209Inferred_automaticallyRNAi_primary
Expr_patternChronogram508
Expr5422
Expr5423
Expr1011813
Expr1037035
Expr1145917
Expr2009323
Expr2027559
Drives_constructWBCnstr00003972
WBCnstr00003973
WBCnstr00028087
Construct_productWBCnstr00028087
Microarray_results (39)
Expression_cluster (202)
Interaction (28)
Map_infoMapIIPosition-1.9316
PositivePositive_cloneC34F11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (4)
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