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WormBase Tree Display for Gene: WBGene00000112

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Name Class

WBGene00000112SMapS_parentSequenceY57G7A
IdentityVersion2
NameCGC_namealh-6Person_evidenceWBPerson651
Sequence_nameF56D12.1
Molecular_name (13)
Other_namexrep-2Paper_evidenceWBPaper00051108
CELE_F56D12.1Accession_evidenceNDBBX284602
Public_namealh-6
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:20WBPerson1971EventImportedInitial conversion from geneace
216 May 2017 09:45:54WBPerson2970Name_changeOther_namexrep-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classalh
Allele (200)
RNASeq_FPKM (74)
GO_annotation (14)
Contained_in_operonCEOP2044
Ortholog (43)
Paralog (11)
Structured_descriptionConcise_descriptionalh-6 is orthologous to the human gene ALDEHYDE DEHYDROGENASE 4 FAMILY, MEMBER A1 (ALDH4A1; OMIM:606811), which when mutated leads to hyperprolinemia type II.Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable 1-pyrroline-5-carboxylate dehydrogenase activity. Predicted to be involved in proline catabolic process to glutamate. Predicted to be located in mitochondrial matrix. Expressed in head and tail. Human ortholog(s) of this gene implicated in hyperprolinemia type 2. Is an ortholog of human ALDH4A1 (aldehyde dehydrogenase 4 family member A1).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:0080543Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:406)
Molecular_infoCorresponding_CDSF56D12.1a
F56D12.1b
F56D12.1c
F56D12.1d
Corresponding_transcriptF56D12.1a.1
F56D12.1a.2
F56D12.1b.1
F56D12.1c.1
F56D12.1d.1
Other_sequenceEX550623.1
HCC09674_1
AYC02886_1
Acan_isotig07901
OFC01683_1
Tcol_isotig02064
HGC01171_1
FD515795.1
CBC00021_1
EX535600.1
OF01268
EX534515.1
HSC01446_1
PP01492
AE03803
CGC00088_1
HC02003
EY466051.1
PPC00477_1
FC545267.1
FC541742.1
CB299778.1
OF01267
FD517494.1
ACC38064_1
BXC07485_1
FC544460.1
Dviv_isotig14949
CJC05786_1
HS01347
HC04580
FK808616.1
FC552657.1
Oden_isotig08810
EY468896.1
BXC06891_1
EX535210.1
ACC21587_1
HG08127
ACC07842_1
Oden_isotig08808
EX535850.1
Dviv_isotig14950
FK803975.1
Name_isotig02288
Oden_isotig08809
Tcir_isotig06613
Oden_isotig08807
Hbac_isotig02400
Acan_isotig13782
JI165882.1
CSC00545_1
Tcol_isotig17151
FC552172.1
Tcir_isotig02557
OFC00244_1
FC540750.1
Tcol_isotig25505
CJC00406_1
EX565682.1
HCC03152_1
Tcir_isotig02556
CBC07829_1
EX555546.1
ACC35431_1
HG10251
BM00482
BMC17384_1
Associated_feature (11)
Experimental_infoRNAi_result (13)
Expr_patternChronogram1568
Expr6220
Expr1014020
Expr1030059
Expr1152446
Expr2009308
Expr2027544
Drives_constructWBCnstr00002586
Regulate_expr_clusterWBPaper00059231:alh-6(lax105)_D3Adult_downregulated
WBPaper00059231:alh-6(lax105)_D3Adult_upregulated
WBPaper00059231:alh-6(lax105)_L4_downregulated
WBPaper00059231:alh-6(lax105)_L4_upregulated
Microarray_results (44)
Expression_cluster (137)
Interaction (68)
Map_infoMapIIPosition-15.5079Error0.004302
PositivePositive_cloneF56D12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00040958
WBPaper00041713
WBPaper00042257
WBPaper00044733
WBPaper00045841
WBPaper00047646
WBPaper00051108
WBPaper00052171
WBPaper00055090
WBPaper00057533
WBPaper00060917
WBPaper00062816
WBPaper00063995
WBPaper00064934
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