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WormBase Tree Display for Gene: WBGene00001872

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Name Class

WBGene00001872SMapS_parentSequenceZK1127
IdentityVersion1
NameCGC_namehim-14Person_evidenceWBPerson261
Sequence_nameZK1127.11
Molecular_nameZK1127.11
ZK1127.11.1
CE24714
Other_nameCELE_ZK1127.11Accession_evidenceNDBBX284602
Public_namehim-14
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhim
Reference_alleleWBVar00088021
Allele (44)
Legacy_information[C.elegansII] it44ts : viable self-progeny 2--40% male,95% dead eggs, probable generalized nondisjunction,meiotic defect. OA4: it13, it21, it23, it52 (strongest allele, <3% eggs hatch). [Kemphues et al. 1988]
StrainWBStrain00029021
WBStrain00023558
WBStrain00000291
RNASeq_FPKM (74)
GO_annotation (21)
Ortholog (34)
ParalogWBGene00003418Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003421Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003422Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionhim-14 encodes a germline-specific member of the MutS family of DNA mismatch repair (MMR) proteins that is orthologous to human MSH4 and Saccharomyces cerevisiae Msh4p; during the pachytene stage of meiosis, HIM-14 activity is required for promoting crossing over between homologous chromosomes and thus, for chiasmata formation and proper chromosome segregation; in contrast, HIM-14 activity does not appear to be required for mismatch repair, nor for chromosome pairing or synapsis; him-14 mRNA expression is detected exclusively in the germline.Paper_evidenceWBPaper00001109
WBPaper00003779
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated18 Dec 2006 00:00:00
Automated_descriptionPredicted to enable double-stranded DNA binding activity. Involved in chiasma assembly; embryo development; and resolution of meiotic recombination intermediates. Located in nucleus. Expressed in embryonic cell and gonad. Human ortholog(s) of this gene implicated in primary ovarian insufficiency and spermatogenic failure 2. Is an ortholog of human MSH4 (mutS homolog 4).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:5426Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7327)
DOID:0070164Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7327)
Molecular_infoCorresponding_CDSZK1127.11
Corresponding_transcriptZK1127.11.1
Other_sequenceCR07984
JI167587.1
CBC06908_1
CRC02643_1
Associated_featureWBsf223282
WBsf223283
Experimental_infoRNAi_result (36)
Expr_patternExpr12974
Expr1025657
Expr1031101
Expr1162552
Expr2012423
Expr2030659
Drives_constructWBCnstr00001712
WBCnstr00020969
WBCnstr00036638
Construct_productWBCnstr00036638
Microarray_results (21)
Expression_cluster (136)
Interaction (51)
WBProcessWBbiopr:00000099
Map_infoMapIIPosition0.475478Error0.021331
Well_ordered
PositivePositive_cloneZK1127Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point3787
Multi_point1391
4542
Pos_neg_data4475
Reference (40)
MethodGene