WormBase Tree Display for Gene: WBGene00016191
expand all nodes | collapse all nodes | view schema
WBGene00016191 | SMap | S_parent | Sequence | C28G1 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 1 | |||||||
Name | Sequence_name | C28G1.6 | |||||||
Molecular_name | C28G1.6 | ||||||||
C28G1.6.1 | |||||||||
CE30885 | |||||||||
Other_name | CELE_C28G1.6 | Accession_evidence | NDB | BX284606 | |||||
Public_name | C28G1.6 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 28 May 2004 13:30:57 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Allele (27) | |||||||||
Strain | WBStrain00055379 | ||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00084528 | ||||||||
00121873 | |||||||||
Ortholog (204) | |||||||||
Paralog (22) | |||||||||
Structured_description | Automated_description | Predicted to enable zinc ion binding activity. Human ortholog(s) of this gene implicated in several diseases, including Henoch-Schoenlein purpura; Sweet syndrome; and hematologic cancer (multiple). Is an ortholog of several human genes including MEFV (MEFV innate immunity regulator, pyrin); TRIM21 (tripartite motif containing 21); and TRIM27 (tripartite motif containing 27). | 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:4947 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:18064) | ||||
DOID:850 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
DOID:2987 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
DOID:9952 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
DOID:0050908 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
DOID:0080746 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
DOID:2841 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
DOID:11123 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
DOID:9538 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
DOID:9119 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6998) | ||||||
Molecular_info | Corresponding_CDS | C28G1.6 | |||||||
Corresponding_transcript | C28G1.6.1 | ||||||||
Associated_feature | WBsf654240 | ||||||||
WBsf237726 | |||||||||
Transcription_factor | WBTranscriptionFactor000411 | ||||||||
Experimental_info | RNAi_result | WBRNAi00041424 | Inferred_automatically | RNAi_primary | |||||
Expr_pattern | Expr1012035 | ||||||||
Expr1145454 | |||||||||
Expr2001203 | |||||||||
Expr2019425 | |||||||||
Drives_construct | WBCnstr00028257 | ||||||||
Construct_product | WBCnstr00028257 | ||||||||
Microarray_results (12) | |||||||||
Expression_cluster (121) | |||||||||
Interaction (14) | |||||||||
Map_info | Positive | Positive_clone | C28G1 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
Interpolated_map_position | X | 0.417489 | |||||||
Reference | WBPaper00027309 | ||||||||
WBPaper00027315 | |||||||||
WBPaper00038491 | |||||||||
WBPaper00055090 | |||||||||
Method | Gene |