WormBase Tree Display for Gene: WBGene00011262
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WBGene00011262 | SMap | S_parent | Sequence | R13H4 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | pho-8 | Person_evidence | WBPerson411 | |||||
WBPerson261 | |||||||||
Sequence_name | R13H4.3 | ||||||||
Molecular_name | R13H4.3 | ||||||||
R13H4.3.1 | |||||||||
CE43107 | |||||||||
Other_name | CELE_R13H4.3 | Accession_evidence | NDB | BX284605 | |||||
Public_name | pho-8 | ||||||||
DB_info | Database | AceView | gene | 5M313 | |||||
WormQTL | gene | WBGene00011262 | |||||||
WormFlux | gene | WBGene00011262 | |||||||
NDB | locus_tag | CELE_R13H4.3 | |||||||
Panther | gene | CAEEL|WormBase=WBGene00011262|UniProtKB=P90949 | |||||||
family | PTHR11567 | ||||||||
NCBI | gene | 179621 | |||||||
RefSeq | protein | NM_073582.5 | |||||||
TrEMBL | UniProtAcc | P90949 | |||||||
UniProt_GCRP | UniProtAcc | P90949 | |||||||
OMIM | gene | 606362 | |||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 26 May 2004 16:54:52 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
2 | 04 Nov 2008 10:21:23 | WBPerson2970 | Name_change | CGC_name | pho-8 | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | pho | ||||||||
Allele (37) | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00049569 | ||||||||
00049570 | |||||||||
Ortholog (34) | |||||||||
Paralog (23) | |||||||||
Structured_description | Automated_description | Predicted to enable phosphatase activity. Predicted to be involved in dephosphorylation. Human ortholog(s) of this gene implicated in amelogenesis imperfecta type 1J. Is an ortholog of human ACP2 (acid phosphatase 2, lysosomal) and ACP4 (acid phosphatase 4). | 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:0080953 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14376) | ||||
Molecular_info | Corresponding_CDS | R13H4.3 | |||||||
Corresponding_CDS_history | R13H4.3:wp195 | ||||||||
Corresponding_transcript | R13H4.3.1 | ||||||||
Other_sequence | HGC07463_1 | ||||||||
CRC08827_1 | |||||||||
Oden_isotig14541 | |||||||||
CJC18201_1 | |||||||||
Oden_isotig14542 | |||||||||
CR04016 | |||||||||
HG07302 | |||||||||
Experimental_info | RNAi_result | WBRNAi00051938 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00034929 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00017848 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00051939 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Expr1026966 | ||||||||
Expr1155583 | |||||||||
Expr2014911 | |||||||||
Expr2033147 | |||||||||
Microarray_results (19) | |||||||||
Expression_cluster (240) | |||||||||
Interaction (11) | |||||||||
Map_info | Map | V | Position | 3.40557 | Error | 0.003351 | |||
Positive | Positive_clone | R13H4 | 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 |