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: WBGene00021304

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00021304SMapS_parentSequenceY32G9A
IdentityVersion2
NameCGC_namenphp-2Paper_evidenceWBPaper00040842
Sequence_nameY32G9A.6
Molecular_name (20)
Other_nameCELE_Y32G9A.6Accession_evidenceNDBBX284605
Public_namenphp-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:04WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
211 Apr 2012 13:49:30WBPerson2970Name_changeCGC_namenphp-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnphp
Allele (226)
StrainWBStrain00036591
RNASeq_FPKM (74)
GO_annotation00000990
00000991
00092081
00092082
00092083
Ortholog (16)
ParalogWBGene00006780Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionnphp-2 encodes an ankyrin repeat domain-containing protein orthologous to mammalian inversin (INVS); NPHP-2 activity is required for ciliogenesis; in regulating ciliogenesis, nphp-2 functions together with nphp-1, nphp-2, and mks-1, mks-3, mks-6, mksr-1 and mksr-2; NPHP-2 localizes to the middle segment of sensory cilium (nonmotile primary cilium).Paper_evidenceWBPaper00040842
Curator_confirmedWBPerson1843
WBPerson324
Date_last_updated23 Oct 2014 00:00:00
Automated_descriptionInvolved in protein localization to ciliary inversin compartment. Located in ciliary inversin compartment. Expressed in neurons. Human ortholog(s) of this gene implicated in hypertension and nephronophthisis 2. Is an ortholog of human INVS (inversin).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:0111113Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17870)
DOID:10763Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17870)
Molecular_infoCorresponding_CDSY32G9A.6a
Y32G9A.6b
Y32G9A.6c
Y32G9A.6d
Y32G9A.6e
Y32G9A.6f
Corresponding_CDS_historyY32G9A.6:wp231
Corresponding_transcriptY32G9A.6g
Y32G9A.6h
Y32G9A.6a.1
Y32G9A.6b.1
Y32G9A.6c.1
Y32G9A.6d.1
Y32G9A.6e.1
Y32G9A.6f.1
Other_sequenceJI468614.1
JI479380.1
Acan_isotig04188
ASC39508_1
JI467427.1
FE909386.1
JI166629.1
JI166462.1
Associated_featureWBsf047485
WBsf646687
WBsf646688
WBsf718287
WBsf999415
WBsf999416
WBsf1019235
WBsf1019236
Experimental_infoRNAi_resultWBRNAi00055798Inferred_automaticallyRNAi_primary
Expr_patternExpr3730
Expr9983
Expr9984
Expr14514
Expr1020265
Expr1039287
Expr1159332
Expr2014366
Expr2032607
Drives_constructWBCnstr00011634
WBCnstr00014987
WBCnstr00014988
WBCnstr00041066
Construct_productWBCnstr00014988
WBCnstr00041066
Microarray_results (16)
Expression_cluster (100)
Map_infoMapVPosition-16.8496
PositivePositive_cloneY32G9AInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00026601
WBPaper00038491
WBPaper00040842
WBPaper00044991
WBPaper00045913
WBPaper00046152
WBPaper00055090
WBPaper00063946
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