Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00003911

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00003911SMapS_parentSequenceC09B8
IdentityVersion1
NameCGC_namepak-1Person_evidenceWBPerson516
Sequence_nameC09B8.7
Molecular_nameC09B8.7a
C09B8.7a.1
CE27670
C09B8.7b
CE06792
C09B8.7c
CE33559
C09B8.7b.1
C09B8.7c.1
Other_nameCePAK
CELE_C09B8.7Accession_evidenceNDBBX284606
Public_namepak-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpak
Allele (77)
StrainWBStrain00031427
WBStrain00000137
RNASeq_FPKM (74)
GO_annotation (49)
Ortholog (37)
Paralog (27)
Structured_descriptionConcise_descriptionpak-1 encodes, by alternative splicing, at least five isoforms of aputative p21-activated kinase orthologous to human PAK1, PAK2 (OMIM:?),and PAK3 (OMIM:300142, mutated in nonsyndromic mental retardation);PAK-1 is required (redundantly with its paralog, MAX-2) for normalaxonal guidance of motoneurons, P cell migration, and locomotion, withmax-2(cy2);pak-1(ok448) double mutants phenotypically resembling unc-73or ced-10;mig-2 mutants; pak-1 is expressed in pharyngeal muscles, CANneurons, ventral cord motoneurons, migrating distal tip cells,developing uterus, B, Y, and T cells in the male tail, and vulval musclecells; by itself, the null pak-1(ok448) mutation has no known phenotype.Paper_evidenceWBPaper00003060
WBPaper00028729
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated31 Jan 2007 00:00:00
Automated_descriptionEnables GTP binding activity and protein kinase activity. Involved in several processes, including anatomical structure morphogenesis; hemidesmosome assembly; and inductive cell migration. Located in several cellular components, including axon; hemidesmosome; and neuronal cell body. Expressed in several structures, including P5.p hermaphrodite; P7.p hermaphrodite; gonad; hypodermis; and neurons. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; carcinoma (multiple); kidney cancer (multiple); and non-syndromic X-linked intellectual disability 30. Is an ortholog of human PAK1 (p21 (RAC1) activated kinase 1); PAK2 (p21 (RAC1) activated kinase 2); and PAK3 (p21 (RAC1) activated kinase 3).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:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8590)
DOID:2154Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8590)
DOID:0112051Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8592)
DOID:2671Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8590)
DOID:4450Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8590)
DOID:0060074Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8591)
EFO:MONDO:0800166Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8591)
DOID:4001Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8590)
DOID:1612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8590)
DOID:5419Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8590)
Molecular_infoCorresponding_CDSC09B8.7a
C09B8.7b
C09B8.7c
Corresponding_CDS_historyC09B8.7d:wp135
C09B8.7e:wp275
Corresponding_transcriptC09B8.7a.1
C09B8.7b.1
C09B8.7c.1
Other_sequence (45)
Associated_feature (12)
Experimental_infoRNAi_result (16)
Expr_pattern (13)
Drives_constructWBCnstr00005467
WBCnstr00008104
WBCnstr00012501
WBCnstr00015511
WBCnstr00018256
WBCnstr00035801
WBCnstr00041561
Construct_productWBCnstr00008104
WBCnstr00012501
WBCnstr00015511
WBCnstr00018885
WBCnstr00035801
WBCnstr00041561
AntibodyWBAntibody00000121
Microarray_results (37)
Expression_cluster (124)
Interaction (222)
Map_infoMapXPosition-3.80222Error0.008236
PositivePositive_cloneC09B8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4344
4562
5639
Pseudo_map_position
ReferenceWBPaper00002544
WBPaper00003060
WBPaper00006196
WBPaper00017244
WBPaper00027245
WBPaper00027258
WBPaper00028086
WBPaper00028483
WBPaper00028729
WBPaper00028985
WBPaper00030275
WBPaper00031901
WBPaper00032371
WBPaper00033547
WBPaper00034902
WBPaper00035085
WBPaper00035198
WBPaper00035583
WBPaper00035946
WBPaper00035978
WBPaper00036905
WBPaper00038193
WBPaper00038247
WBPaper00038491
WBPaper00038583
WBPaper00041589
WBPaper00041761
WBPaper00042159
WBPaper00042732
WBPaper00042736
WBPaper00042750
WBPaper00042774
WBPaper00043327
WBPaper00044122
WBPaper00044916
WBPaper00045130
WBPaper00045213
WBPaper00048266
WBPaper00048282
WBPaper00050415
WBPaper00052174
WBPaper00052186
WBPaper00052195
WBPaper00052206
WBPaper00052209
WBPaper00054435
WBPaper00055090
WBPaper00055350
WBPaper00057243
WBPaper00057687
WBPaper00057701
WBPaper00058347
WBPaper00060685
WBPaper00061399
WBPaper00061553
WBPaper00064323
WBPaper00064400
WBPaper00064670
WBPaper00064789
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