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
Reference (60)
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