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: WBGene00004737

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00004737EvidenceCGC_data_submission
SMapS_parentSequenceF10G7
IdentityVersion1
NameCGC_namescc-1Person_evidenceWBPerson421
Sequence_nameF10G7.4
Molecular_nameF10G7.4
F10G7.4.1
CE02628
Other_namecoh-2Person_evidenceWBPerson421
WBPerson1819
rad-21.1
CELE_F10G7.4Accession_evidenceNDBBX284602
Public_namescc-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classscc
Allele (26)
Legacy_information[J. Loidl] RNAi phenotypes : ~98% embryo lethality, HIM (~3% males); protein localizes to somatic nuclei of the embryo and to nuclei at meiotic prophase
[J. Loidl] (F10G7.4) is homolog to the Rad21/Scc1/Rec8 family of cohesion proteins with knownmembers in S. cerevisiae, S. pombe, A. thaliana and vertebrates. R-S-R is the acronym of the founder family.
StrainWBStrain00035987
RNASeq_FPKM (74)
GO_annotation (20)
Ortholog (44)
ParalogWBGene00000591Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
Structured_descriptionConcise_descriptionscc-1 encodes a member of the Rad21/Rec8-like family of cohesion proteins that affects embryonic viability, fertility, the rate of embryonic cell divisions and the incidence of male progeny; interacts with ATL-1, F56D12.5, and F11E6.1 based on yeast two-hybrid assays, and is expressed in nondividing embryonic and germline nuclei.Paper_evidenceWBPaper00004651
WBPaper00004722
WBPaper00005039
WBPaper00018377
Curator_confirmedWBPerson48
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable chromatin binding activity and damaged DNA binding activity. Involved in meiotic cell cycle. Located in nucleus. Part of cohesin complex. Expressed in several structures, including SDQ; germ line; seam cell; touch receptor neurons; and ventral nerve cord. Human ortholog(s) of this gene implicated in Cornelia de Lange syndrome 4; carcinoma (multiple); and endometrial cancer. Is an ortholog of human RAD21 (RAD21 cohesin complex component) and RAD21L1 (RAD21 cohesin complex component like 1).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:0080508Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9811)
DOID:0050866Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9811)
DOID:3908Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9811)
DOID:0080199Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9811)
DOID:684Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9811)
DOID:1380Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9811)
Molecular_infoCorresponding_CDSF10G7.4
Corresponding_transcriptF10G7.4.1
Other_sequenceCRC06495_1
MP00107
BXC03089_1
CBC02363_1
MI06164
CJC04977_1
CR03754
RSC00091_1
CJC01832_1
MIC05797_1
Associated_featureWBsf644122
WBsf987674
WBsf221156
Experimental_infoRNAi_result (17)
Expr_patternExpr1350
Expr2579
Expr11962
Expr1015315
Expr1032337
Expr1148255
Expr2015621
Expr2033856
Drives_constructWBCnstr00035420
Construct_productWBCnstr00035420
AntibodyWBAntibody00000375
WBAntibody00000636
WBAntibody00000645
WBAntibody00000646
Microarray_results (19)
Expression_cluster (151)
Interaction (107)
WBProcessWBbiopr:00000099
Map_infoMapIIPosition-3.59162Error0.111344
PositivePositive_cloneF10G7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4996
Pseudo_map_position
Reference (13)
RemarkSequence connection from [Sugimoto A]
Map 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