WormBase Tree Display for Gene: WBGene00023491
expand all nodes | collapse all nodes | view schema
WBGene00023491 | SMap | S_parent | Sequence | C17G1 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | tsp-21 | Person_evidence | WBPerson522 | |||||
Sequence_name | C17G1.8 | ||||||||
Molecular_name | C17G1.8 | ||||||||
C17G1.8.1 | |||||||||
CE42559 | |||||||||
C17G1.8.2 | |||||||||
Other_name | CELE_C17G1.8 | Accession_evidence | NDB | BX284606 | |||||
Public_name | tsp-21 | ||||||||
DB_info | Database | AceView | gene | XK557 | |||||
WormFlux | gene | WBGene00023491 | |||||||
NDB | locus_tag | CELE_C17G1.8 | |||||||
Panther | gene | CAEEL|WormBase=WBGene00023491|UniProtKB=Q5WRN1 | |||||||
family | PTHR19282 | ||||||||
NCBI | gene | 259720 | |||||||
RefSeq | protein | NM_001383631.2 | |||||||
SwissProt | UniProtAcc | Q5WRN1 | |||||||
UniProt_GCRP | UniProtAcc | Q5WRN1 | |||||||
OMIM | gene | 613138 | |||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 24 Aug 2004 09:31:59 | WBPerson1846 | Event | Created | |||
2 | 29 Aug 2008 15:37:08 | WBPerson2970 | Name_change | CGC_name | tsp-21 | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | tsp | ||||||||
Allele (82) | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation (16) | |||||||||
Ortholog (42) | |||||||||
Paralog (20) | |||||||||
Structured_description | Automated_description | Enables identical protein binding activity. Involved in positive regulation of signal transduction; regulation of growth; and regulation of mesodermal cell fate specification. Located in basolateral plasma membrane. Expressed in several structures, including M lineage cell; gonad; intestine; rectal epithelium; and vulva. Used to study cancer. Human ortholog(s) of this gene implicated in exudative vitreoretinopathy 5. Is an ortholog of human CD53 (CD53 molecule) and TSPAN12 (tetraspanin 12). | 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 | Experimental_model | DOID:162 | Homo sapiens | Paper_evidence | WBPaper00046810 | ||||
Curator_confirmed | WBPerson324 | ||||||||
Date_last_updated | 15 Jul 2015 00:00:00 | ||||||||
Potential_model | DOID:0111408 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:21641) | |||||
Models_disease_in_annotation | WBDOannot00000355 | ||||||||
Molecular_info | Corresponding_CDS | C17G1.8 | |||||||
Corresponding_CDS_history | C17G1.8:wp190 | ||||||||
Corresponding_transcript | C17G1.8.1 | ||||||||
C17G1.8.2 | |||||||||
Other_sequence | CBC12790_1 | ||||||||
Oden_isotig20087 | |||||||||
EX557416.1 | |||||||||
ACC20644_1 | |||||||||
CRC05977_1 | |||||||||
EX827951.1 | |||||||||
CR10547 | |||||||||
Associated_feature | WBsf662382 | ||||||||
WBsf663211 | |||||||||
WBsf663212 | |||||||||
WBsf982222 | |||||||||
WBsf1006573 | |||||||||
WBsf236216 | |||||||||
Experimental_info | Expr_pattern | Expr12377 | |||||||
Expr12378 | |||||||||
Expr1010952 | |||||||||
Expr1040139 | |||||||||
Expr1144878 | |||||||||
Expr2017551 | |||||||||
Expr2035689 | |||||||||
Drives_construct | WBCnstr00020524 | ||||||||
WBCnstr00023858 | |||||||||
Construct_product | WBCnstr00020524 | ||||||||
WBCnstr00023858 | |||||||||
Microarray_results (13) | |||||||||
Expression_cluster (67) | |||||||||
Interaction | WBInteraction000525308 | ||||||||
WBInteraction000525309 | |||||||||
WBInteraction000551376 | |||||||||
WBInteraction000551377 | |||||||||
WBInteraction000551378 | |||||||||
Map_info | Map | X | Position | 1.7312 | |||||
Positive | Positive_clone | C17G1 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
Pseudo_map_position | |||||||||
Reference | WBPaper00038491 | ||||||||
WBPaper00046810 | |||||||||
WBPaper00048314 | |||||||||
WBPaper00055090 | |||||||||
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 |