WormBase Tree Display for Gene: WBGene00008598
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WBGene00008598 | SMap | S_parent | Sequence | F09A5 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | spin-3 | Paper_evidence | WBPaper00042308 | |||||
Sequence_name | F09A5.1 | ||||||||
Molecular_name | F09A5.1 | ||||||||
F09A5.1.1 | |||||||||
CE40809 | |||||||||
Other_name | CELE_F09A5.1 | Accession_evidence | NDB | BX284606 | |||||
Public_name | spin-3 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 26 May 2004 16:54:49 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
2 | 04 Jun 2013 14:47:04 | WBPerson2970 | Name_change | CGC_name | spin-3 | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | spin | ||||||||
Allele (64) | |||||||||
Strain | WBStrain00032469 | ||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00063987 | ||||||||
00063988 | |||||||||
00063989 | |||||||||
00116490 | |||||||||
00116491 | |||||||||
Ortholog (55) | |||||||||
Paralog | WBGene00007549 | Caenorhabditis elegans | From_analysis | Panther | |||||
WormBase-Compara | |||||||||
WBGene00008033 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
Panther | |||||||||
WormBase-Compara | |||||||||
WBGene00013739 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
Panther | |||||||||
WormBase-Compara | |||||||||
Structured_description | Automated_description | Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in membrane. Expressed in amphid neurons; intestine; and retrovesicular ganglion neurons. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 115. Is an ortholog of human SPNS1 (SPNS lysolipid transporter 1, lysophospholipid); SPNS2 (SPNS lysolipid transporter 2, sphingosine-1-phosphate); and SPNS3 (SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)). | Paper_evidence | WBPaper00065943 | |||||
Curator_confirmed | WBPerson324 | ||||||||
WBPerson37462 | |||||||||
Inferred_automatically | This description was generated automatically by a script based on data from the WS291 version of WormBase | ||||||||
Date_last_updated | 29 Nov 2023 00:00:00 | ||||||||
Disease_info | Potential_model | DOID:0111643 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:26992) | ||||
Molecular_info | Corresponding_CDS | F09A5.1 | |||||||
Corresponding_CDS_history | F09A5.1:wp102 | ||||||||
F09A5.1:wp173 | |||||||||
Corresponding_transcript | F09A5.1.1 | ||||||||
Other_sequence | HC05598 | ||||||||
ACC16946_1 | |||||||||
EY471708.1 | |||||||||
Dviv_isotig17614 | |||||||||
HCC07391_1 | |||||||||
Dviv_isotig17615 | |||||||||
Associated_feature | WBsf236537 | ||||||||
Experimental_info | RNAi_result | WBRNAi00030682 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00044069 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00012942 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Expr13201 | ||||||||
Expr1026100 | |||||||||
Expr1148034 | |||||||||
Expr2034294 | |||||||||
Drives_construct | WBCnstr00032841 | ||||||||
WBCnstr00038866 | |||||||||
Construct_product | WBCnstr00032841 | ||||||||
Microarray_results (18) | |||||||||
Expression_cluster (154) | |||||||||
Interaction (11) | |||||||||
Map_info | Map | X | Position | 10.2128 | |||||
Positive | Positive_clone | F09A5 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
Pseudo_map_position | |||||||||
Reference | WBPaper00038491 | ||||||||
WBPaper00055090 | |||||||||
WBPaper00061938 | |||||||||
Remark | 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 | |||||||
Method | Gene |