WormBase Tree Display for Gene: WBGene00000055
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| WBGene00000055 | SMap | S_parent | Sequence | F25G6 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | CGC_name | acr-16 | Person_evidence | WBPerson1430 | |||||
| Sequence_name | F25G6.3 | ||||||||
| Molecular_name | F25G6.3 | ||||||||
| F25G6.3.1 | |||||||||
| CE09639 | |||||||||
| Other_name | Ce21 | ||||||||
| CELE_F25G6.3 | Accession_evidence | NDB | BX284605 | ||||||
| Public_name | acr-16 | ||||||||
| DB_info | Database | AceView | gene | 5J43 | |||||
| WormQTL | gene | WBGene00000055 | |||||||
| WormFlux | gene | WBGene00000055 | |||||||
| NDB | locus_tag | CELE_F25G6.3 | |||||||
| Panther | gene | CAEEL|WormBase=WBGene00000055|UniProtKB=P48180 | |||||||
| family | PTHR18945 | ||||||||
| NCBI | gene | 179235 | |||||||
| RefSeq | protein | NM_072806.5 | |||||||
| SwissProt | UniProtAcc | P48180 | |||||||
| UniProt_GCRP | UniProtAcc | P48180 | |||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:19 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | acr | ||||||||
| Allele | WBVar00464908 | ||||||||
| WBVar00464909 | |||||||||
| WBVar01499903 | |||||||||
| WBVar01825825 | |||||||||
| WBVar01500129 | |||||||||
| WBVar01911116 | |||||||||
| WBVar00092069 | |||||||||
| WBVar01499056 | |||||||||
| WBVar01031776 | |||||||||
| WBVar01031777 | |||||||||
| WBVar01031778 | |||||||||
| WBVar01031779 | |||||||||
| WBVar01031780 | |||||||||
| WBVar01031781 | |||||||||
| WBVar01031782 | |||||||||
| WBVar01031783 | |||||||||
| WBVar01031784 | |||||||||
| WBVar01031785 | |||||||||
| WBVar01031786 | |||||||||
| WBVar01031787 | |||||||||
| WBVar01031788 | |||||||||
| WBVar01031789 | |||||||||
| WBVar01031790 | |||||||||
| WBVar01848372 | |||||||||
| WBVar00250010 | |||||||||
| WBVar01661211 | |||||||||
| WBVar01651980 | |||||||||
| WBVar01499316 | |||||||||
| WBVar00464899 | |||||||||
| WBVar00464900 | |||||||||
| WBVar00464901 | |||||||||
| WBVar00464902 | |||||||||
| WBVar00464903 | |||||||||
| WBVar00464904 | |||||||||
| WBVar00464905 | |||||||||
| WBVar00464906 | |||||||||
| WBVar00464907 | |||||||||
| Strain | WBStrain00031630 | ||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (32) | |||||||||
| Ortholog (42) | |||||||||
| Paralog (100) | |||||||||
| Structured_description | Concise_description | acr-16 encodes an alpha-7-like homomer-forming subunit of the nicotinic acetylcholine receptor (nAChR) superfamily orthologous to human nicotinic cholinergic receptor alpha 7 (CHRNA7; OMIM:118511; possibly associated with schizophrenia and juvenile myoclonic epilepsy); ACR-16 functions as a ligand-gated ion channel that is required for the major fast cholinergic excitatory current at C. elegans neuromuscular junctions; when expressed in Xenopus ooctyes, ACR-16 is active as a homomeric receptor and responds robustly to acetylcholine; an ACR-16::GFP reporter fusion expressed in muscle cells localizes to the tips of muscle arms, specific regions of the muscle cell membrane that form synapses with neuronal processes; acr-16::gfp promoter fusions also reveal expression in a subset of neurons; ACR-16 localization to postsynaptic regions, a key component of activity-dependent synaptic plasticity, is regulated by a Wnt signaling pathway that includes CWN-2, LIN-17, CAM-1, and DSH-1. | Paper_evidence | WBPaper00003425 | |||||
| WBPaper00004459 | |||||||||
| WBPaper00005427 | |||||||||
| WBPaper00005594 | |||||||||
| WBPaper00025245 | |||||||||
| WBPaper00040939 | |||||||||
| Curator_confirmed | WBPerson1843 | ||||||||
| WBPerson1823 | |||||||||
| WBPerson567 | |||||||||
| Date_last_updated | 17 Apr 2012 00:00:00 | ||||||||
| Automated_description | Enables acetylcholine-gated monoatomic cation-selective channel activity. Involved in monoatomic ion transmembrane transport. Located in cell projection. Expressed in body wall musculature; linker cell; muscle cell; and neurons. Used to study nicotine dependence. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; Lewy body dementia; carcinoma (multiple); and inflammatory bowel disease (multiple). Is an ortholog of human CHRFAM7A (CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion) and CHRNA7 (cholinergic receptor nicotinic alpha 7 subunit). | 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:0050742 | Homo sapiens | Paper_evidence | WBPaper00028761 | ||||
| Curator_confirmed | WBPerson324 | ||||||||
| Date_last_updated | 22 May 2019 00:00:00 | ||||||||
| Potential_model | DOID:10652 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | |||||
| DOID:3908 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| DOID:3748 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| DOID:8778 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| DOID:3083 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| DOID:12217 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| DOID:8577 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| DOID:1324 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| DOID:7474 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| DOID:5419 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1960) | ||||||
| Models_disease_asserted | WBDOannot00000676 | ||||||||
| Molecular_info | Corresponding_CDS | F25G6.3 | |||||||
| Corresponding_CDS_history | F25G6.3a:wp246 | ||||||||
| F25G6.3b:wp246 | |||||||||
| Corresponding_transcript | F25G6.3.1 | ||||||||
| Other_sequence (27) | |||||||||
| Associated_feature | WBsf1000696 | ||||||||
| WBsf1000697 | |||||||||
| WBsf232121 | |||||||||
| Experimental_info | RNAi_result (11) | ||||||||
| Expr_pattern (13) | |||||||||
| Drives_construct | WBCnstr00004901 | ||||||||
| WBCnstr00004902 | |||||||||
| WBCnstr00004903 | |||||||||
| WBCnstr00004904 | |||||||||
| WBCnstr00004905 | |||||||||
| WBCnstr00009872 | |||||||||
| WBCnstr00011440 | |||||||||
| WBCnstr00011957 | |||||||||
| WBCnstr00017746 | |||||||||
| WBCnstr00018183 | |||||||||
| Construct_product | WBCnstr00001360 | ||||||||
| WBCnstr00006788 | |||||||||
| WBCnstr00009355 | |||||||||
| WBCnstr00011441 | |||||||||
| WBCnstr00014504 | |||||||||
| WBCnstr00020316 | |||||||||
| Antibody | WBAntibody00001986 | ||||||||
| Microarray_results (30) | |||||||||
| Expression_cluster (125) | |||||||||
| Interaction (28) | |||||||||
| Map_info | Map | V | Position | 1.46223 | Error | 0.003864 | |||
| Positive | Positive_clone | F25G6 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Mapping_data | Multi_point | 4869 | |||||||
| 5605 | |||||||||
| Pseudo_map_position | |||||||||
| Reference (89) | |||||||||
| 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 |
