WormBase Tree Display for Gene: WBGene00006770
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WBGene00006770 | SMap | S_parent | Sequence | Y50D4C | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | unc-34 | Person_evidence | WBPerson261 | |||||
Sequence_name | Y50D4C.1 | ||||||||
Molecular_name (21) | |||||||||
Other_name | CELE_Y50D4C.1 | Accession_evidence | NDB | BX284605 | |||||
Public_name | unc-34 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 07 Apr 2004 11:29:42 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
2 | 02 Mar 2018 11:09:16 | WBPerson4025 | Event | Split_into | WBGene00303091 | ||||
Split_into | WBGene00303091 | ||||||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | unc | ||||||||
Reference_allele | WBVar00143110 | ||||||||
Allele (349) | |||||||||
Legacy_information | e315ts : at 20x fairly severe coiler somewhat active grows well; male has crumpled copulatory spicules; variable defects in VD and DD commissures; at 15x moves much better. ES3 (20x) ME0. NA3 (e566 e951pdi : non-ts alleles coilers at all temperatures; e566 strongest allele). | ||||||||
See also s138 | |||||||||
[C.elegansII] e315ts : at 20C fairly severe coiler, somewhat active, grows well; male has crumpled copulatory spicules; variable defects in VD and DD commissures; At 15C moves much better. Low penetrance withered tail phenotype (CAN cell defect),and excretory cell abnormalities.ES3 (20C) ME0. OA>5: e566, (strongest allele,non-ts, coils at all temperatures; defects in axonal elongation and fasciculation), e951pdi, s138gri, etc. [Brenner 1974; McIntire et al. 1992; CX; NG; NW; MT] | |||||||||
Strain | WBStrain00022543 | ||||||||
WBStrain00024076 | |||||||||
WBStrain00024143 | |||||||||
WBStrain00027135 | |||||||||
WBStrain00027253 | |||||||||
WBStrain00031248 | |||||||||
WBStrain00004147 | |||||||||
WBStrain00004181 | |||||||||
WBStrain00051845 | |||||||||
WBStrain00053139 | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00001039 | ||||||||
00019523 | |||||||||
00019524 | |||||||||
00019525 | |||||||||
00019526 | |||||||||
00019527 | |||||||||
00019528 | |||||||||
00019529 | |||||||||
00019530 | |||||||||
00019531 | |||||||||
00019532 | |||||||||
00019533 | |||||||||
00019534 | |||||||||
00019535 | |||||||||
Ortholog (45) | |||||||||
Structured_description (2) | |||||||||
Disease_info | Experimental_model | DOID:680 | Homo sapiens | Paper_evidence | WBPaper00030773 | ||||
Curator_confirmed | WBPerson324 | ||||||||
Date_last_updated | 15 Oct 2018 00:00:00 | ||||||||
Potential_model | DOID:684 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:18271) | |||||
Models_disease_asserted | WBDOannot00000620 | ||||||||
Molecular_info | Corresponding_CDS | Y50D4C.1a | |||||||
Y50D4C.1b | |||||||||
Y50D4C.1c | |||||||||
Y50D4C.1d | |||||||||
Y50D4C.1e | |||||||||
Y50D4C.1f | |||||||||
Y50D4C.1g | |||||||||
Corresponding_CDS_history | Y50D4C.1:wp90 | ||||||||
Y50D4C.1a:wp196 | |||||||||
Y50D4C.1h:wp264 | |||||||||
Corresponding_transcript | Y50D4C.1a.1 | ||||||||
Y50D4C.1b.1 | |||||||||
Y50D4C.1c.1 | |||||||||
Y50D4C.1d.1 | |||||||||
Y50D4C.1e.1 | |||||||||
Y50D4C.1f.1 | |||||||||
Y50D4C.1g.1 | |||||||||
Other_sequence (21) | |||||||||
Associated_feature (12) | |||||||||
Experimental_info (11) | |||||||||
Map_info | Map | V | Position | -19.8783 | Error | 0.017009 | |||
Well_ordered | |||||||||
Positive | Inside_rearr | yDp1 | |||||||
Positive_clone | Y50D4C | Inferred_automatically | From sequence, transcript, pseudogene data | ||||||
Mapping_data | 2_point | 124 | |||||||
586 | |||||||||
1731 | |||||||||
3138 | |||||||||
3145 | |||||||||
6113 | |||||||||
Multi_point (18) | |||||||||
Pos_neg_data | 3089 | ||||||||
3095 | |||||||||
3104 | |||||||||
3396 | |||||||||
3146 | |||||||||
3147 | |||||||||
5194 | |||||||||
3258 | |||||||||
Reference (145) | |||||||||
Method | Gene |