WormBase Tree Display for Gene: WBGene00185001
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| WBGene00185001 | SMap | S_parent | Sequence | F56A8 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | Sequence_name | F56A8.9 | |||||||
| Molecular_name | F56A8.9 | ||||||||
| F56A8.9.1 | |||||||||
| CE43524 | |||||||||
| Other_name | CELE_F56A8.9 | Accession_evidence | NDB | BX284603 | |||||
| Public_name | F56A8.9 | ||||||||
| DB_info | Database | WormFlux | gene | WBGene00185001 | |||||
| NDB | locus_tag | CELE_F56A8.9 | |||||||
| Panther | gene | CAEEL|WormBase=WBGene00185001|UniProtKB=C0P287 | |||||||
| family | PTHR14735 | ||||||||
| NCBI | gene | 13191724 | |||||||
| RefSeq | protein | NM_001268263.2 | |||||||
| TrEMBL | UniProtAcc | C0P287 | |||||||
| UniProt_GCRP | UniProtAcc | C0P287 | |||||||
| OMIM | gene | 618788 | |||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 11 Feb 2009 14:49:26 | WBPerson1983 | Event | Split_from | WBGene00010138 | ||
| Split_from | WBGene00010138 | ||||||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Allele (44) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| Ortholog (30) | |||||||||
| Structured_description | Automated_description | Enriched in several structures, including ABplpppapa; ABprpppapa; G2; pharyngeal cell; and rectal epithelial cell based on RNA-seq and single-cell RNA-seq studies. Is affected by several genes including skn-1; clk-1; and npr-1 based on RNA-seq and microarray studies. Is affected by six chemicals including rotenone; allantoin; and Sirolimus based on RNA-seq and microarray studies. Human ortholog(s) of this gene implicated in osteogenesis imperfecta. Is predicted to encode a protein with the following domains: ERK and JNK pathways, inhibitor and Coiled-coil domain-containing protein 134. Is an ortholog of human CCDC134 (coiled-coil domain containing 134). | 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:12347 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:26185) | ||||
| Molecular_info | Corresponding_CDS | F56A8.9 | |||||||
| Corresponding_transcript | F56A8.9.1 | ||||||||
| Other_sequence (17) | |||||||||
| Associated_feature | WBsf645694 | ||||||||
| Experimental_info | Expr_pattern | Expr1022593 | |||||||
| Expr1040434 | |||||||||
| Expr1152394 | |||||||||
| Expr2004270 | |||||||||
| Expr2022492 | |||||||||
| Microarray_results (14) | |||||||||
| Expression_cluster (78) | |||||||||
| Map_info | Positive | Positive_clone | F56A8 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | III | 21.144 | |||||||
| Reference | WBPaper00055090 | ||||||||
| Method | Gene |
