WormBase Tree Display for Gene: WBGene00194710
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WBGene00194710 | SMap | S_parent | Sequence | C30B5 | ||
---|---|---|---|---|---|---|
Identity (6) | ||||||
Gene_info | Biotype | SO:0001217 | ||||
Gene_class | mks | |||||
Allele (12) | ||||||
RNASeq_FPKM (74) | ||||||
GO_annotation | 00007025 | |||||
00007026 | ||||||
00007027 | ||||||
00007028 | ||||||
00007029 | ||||||
00007030 | ||||||
00007031 | ||||||
Ortholog (39) | ||||||
Paralog | WBGene00022733 | Caenorhabditis elegans | From_analysis | Panther | ||
Structured_description | Automated_description | Involved in non-motile cilium assembly and protein localization to ciliary transition zone. Located in ciliary transition zone. Human ortholog(s) of this gene implicated in Joubert syndrome 2 and Meckel syndrome 2. Is an ortholog of human TMEM216 (transmembrane protein 216). | 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:0110988 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:25018) | |
DOID:0070116 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:25018) | |||
DOID:0050777 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:25018) | |||
Molecular_info | Corresponding_CDS | C30B5.9 | ||||
Corresponding_CDS_history | C30B5.9:wp224 | |||||
Corresponding_transcript | C30B5.9.1 | |||||
Associated_feature | WBsf650119 | |||||
WBsf665242 | ||||||
WBsf988101 | ||||||
WBsf988102 | ||||||
WBsf988103 | ||||||
Experimental_info | Expr_pattern | Expr1145552 | ||||
Expr2013583 | ||||||
Expr2031816 | ||||||
Microarray_results | 181850_at | |||||
Aff_C30B5.6 | ||||||
GPL19516_CGZ0006717 | ||||||
GPL21109_C30B5.9 | ||||||
Expression_cluster (91) | ||||||
Map_info | Map | II | Position | -0.400561 | ||
Positive | Positive_clone | C30B5 | Inferred_automatically | From sequence, transcript, pseudogene data | ||
Pseudo_map_position | ||||||
Reference | WBPaper00040522 | |||||
WBPaper00046659 | ||||||
WBPaper00048909 | ||||||
WBPaper00049218 | ||||||
WBPaper00049372 | ||||||
WBPaper00052057 | ||||||
WBPaper00053681 | ||||||
WBPaper00055090 | ||||||
WBPaper00060708 | ||||||
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 |