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Gene: F53B2.6   

F53B2.6EvidenceCGC_data_submission
SMapS_parentSequenceSUPERLINK_CB_IV
ChromosomeIV
Identity (5)
Gene_info Gene_classham
Allele (6)
Phenotype[C.elegansII] n1438 : multiple HSN defects, Egl, Dyf; HSN and sister phasmid neuron PHB both abnormal; also disrupted asymmetry in other sister cells RID, ADE/ADA, ADL, ALN/PLM. OA1: n1810. Cloned: 1.8 kb RNA, encodes 414 aa novel protein. [Desai et al. 1988; Garriga and Stern 1994; NG; NH; MT]
StrainMT3551
GO_term (5)
Structured_description Provisional_descriptionham-1 encodes a novel protein with a winged helix DNA-binding motif; ham-1 is required for the asymmetric divisions of several neuroblasts in the developing embryo and may influence their spindle position; ham-1 mutations also exhibit HSN motor neuron migration defects; HAM-1 interacts with itself in a yeast two-hybrid screen and observations suggest that its multimerization is required for its proper localization; HAM-1 is cytoplasmic and is asymmetrically distributed to the posterior of the HSNPHB neuroblast. Paper_evidence WBPaper00001105
WBPaper00002607
WBPaper00019286
Person_evidenceWBPerson324
Curator_confirmedWBPerson324
Date_last_updated17 Jun 2004 00:00:00
Concise_descriptionham-1 encodes a novel protein with a winged helix DNA-binding motif; ham-1 is required for the asymmetric divisions of several neuroblasts in the developing embryo and may influence their spindle position; ham-1 mutations also exhibit HSN motor neuron migration defects; HAM-1 interacts with itself in a yeast two-hybrid screen and observations suggest that its multimerization is required for its proper localization; HAM-1 is cytoplasmic and is asymmetrically distributed to the posterior of the HSNPHB neuroblast.
Molecular_info (5)
Experimental_info RNAi_result Cenix:47-b11
JA:F53B2.6
WB_RNAi_result JA:F53B2.6
MV_SV:mv_F53B2.6
Cenix:47-b11
Expr_pattern Expr1604
Expr3416
Reference (30)
RemarkPrevious connection to hap-1 (ZC395.7) was incorrect [030311 ck1]
MethodGene