WormBase Tree Display for Gene: WBGene00020275
expand all nodes | collapse all nodes | view schema
WBGene00020275 | SMap | S_parent | Sequence | T05H4 | |||
---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||
Name | CGC_name | atp-4 | Person_evidence | WBPerson1157 | |||
Sequence_name | T05H4.12 | ||||||
Molecular_name | T05H4.12 | ||||||
T05H4.12.1 | |||||||
CE13291 | |||||||
T05H4.12.2 | |||||||
Other_name | CELE_T05H4.12 | Accession_evidence | NDB | BX284605 | |||
Public_name | atp-4 | ||||||
DB_info | Database | AceView | gene | 5G906 | |||
WormQTL | gene | WBGene00020275 | |||||
WormFlux | gene | WBGene00020275 | |||||
NDB | locus_tag | CELE_T05H4.12 | |||||
Panther | gene | CAEEL|WormBase=WBGene00020275|UniProtKB=O16517 | |||||
family | PTHR12441 | ||||||
NCBI | gene | 179025 | |||||
RefSeq | protein | NM_001392530.1 | |||||
TrEMBL | UniProtAcc | O16517 | |||||
UniProt_GCRP | UniProtAcc | O16517 | |||||
Species | Caenorhabditis elegans | ||||||
History | Version_change (2) | ||||||
Status | Live | ||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | atp | ||||||
Allele (36) | |||||||
Strain | WBStrain00037564 | ||||||
RNASeq_FPKM (74) | |||||||
GO_annotation (12) | |||||||
Contained_in_operon | CEOP5108 | ||||||
Ortholog (31) | |||||||
Structured_description | Automated_description | Predicted to enable proton transmembrane transporter activity. Predicted to be involved in proton motive force-driven ATP synthesis and proton transmembrane transport. Predicted to be located in mitochondrial inner membrane. Predicted to be part of mitochondrial proton-transporting ATP synthase complex. Human ortholog(s) of this gene implicated in essential hypertension. Is an ortholog of human ATP5PF (ATP synthase peripheral stalk subunit F6). | 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:10825 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:847) | ||
Molecular_info | Corresponding_CDS | T05H4.12 | |||||
Corresponding_transcript | T05H4.12.1 | ||||||
T05H4.12.2 | |||||||
Other_sequence (54) | |||||||
Associated_feature | WBsf652701 | ||||||
WBsf652702 | |||||||
WBsf233795 | |||||||
WBsf233796 | |||||||
WBsf233797 | |||||||
Experimental_info | RNAi_result (35) | ||||||
Expr_pattern | Expr1025885 | ||||||
Expr1038829 | |||||||
Expr1156199 | |||||||
Expr2009512 | |||||||
Expr2027749 | |||||||
Drives_construct | WBCnstr00025246 | ||||||
Construct_product | WBCnstr00025246 | ||||||
Microarray_results (21) | |||||||
Expression_cluster (100) | |||||||
Interaction (49) | |||||||
Map_info (3) | |||||||
Reference | WBPaper00026715 | ||||||
WBPaper00049531 | |||||||
WBPaper00061870 | |||||||
WBPaper00062370 | |||||||
WBPaper00065341 | |||||||
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 |