WormBase Tree Display for Gene: WBGene00302980
expand all nodes | collapse all nodes | view schema
| WBGene00302980 | SMap | S_parent | Sequence | F53E2 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | Sequence_name | F53E2.2 | |||||||
| Molecular_name | F53E2.2 | ||||||||
| F53E2.2.1 | |||||||||
| CE20547 | |||||||||
| Other_name | CELE_F53E2.2 | Accession_evidence | NDB | BX284605 | |||||
| Public_name | F53E2.2 | ||||||||
| DB_info | Database | NDB | locus_tag | CELE_F53E2.2 | |||||
| NCBI | gene | 41657006 | |||||||
| RefSeq | protein | NM_071024.9 | |||||||
| SwissProt | UniProtAcc | Q07750 | |||||||
| UniProt_GCRP | UniProtAcc | Q07750 | |||||||
| OMIM | gene | 601443 | |||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 06 Mar 2018 14:39:08 | WBPerson4025 | Event | Split_from | WBGene00006794 | ||
| Split_from | WBGene00006794 | ||||||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Allele (43) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (36) | |||||||||
| Contained_in_operon | CEOP5600 | ||||||||
| Ortholog (42) | |||||||||
| Paralog | WBGene00006794 | Caenorhabditis elegans | From_analysis | WormBase-Compara | |||||
| Structured_description | Automated_description | Enables actin filament binding activity. Involved in several processes, including actin filament-based process; embryo development; and positive regulation of actin filament polymerization. Located in striated muscle thin filament. Part of ribonucleoprotein complex. Human ortholog(s) of this gene implicated in brain compression; gallbladder carcinoma; and nemaline myopathy 7. Is an ortholog of human CFL2 (cofilin 2). | 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:4948 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1874) | ||||
| DOID:0110934 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1875) | ||||||
| DOID:11457 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:1874) | ||||||
| Molecular_info | Corresponding_CDS | F53E2.2 | |||||||
| Corresponding_transcript | F53E2.2.1 | ||||||||
| Experimental_info | RNAi_result (39) | ||||||||
| Microarray_results (30) | |||||||||
| Expression_cluster (55) | |||||||||
| Interaction | WBInteraction000519090 | ||||||||
| WBInteraction000581343 | |||||||||
| Map_info | Map | V | |||||||
| Positive | Positive_clone | F53E2 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Interpolated_map_position | V | -18.8782 | |||||||
| Method | Gene |
